Former Topics

Collapse allExpand all

 Publications 

H.-U. Reißig*, R. Zimmer
Münchnone – 50 Jahre und ein bisschen weiser

Angew. Chem.
2014, 126, 9864 – 9866.

H.-U. Reißig*, R. Zimmer
Münchnones – New Facets after 50 Years
Angew. Chem. Int. Ed. 2014, 53, 9708 – 9710.

B. Dugovič, H.-U. Reißig*
A New Alkoxyallene-Based [3+2] Approach to the Synthesis of Highly Substituted Cyclopentenones
Synlett 2008, 769 – 773.

B. Dugovič, L. Fišera, H.-U. Reißig*
1,3-Dipolar Cycloadditions of N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone to Methoxyallene – Control of Site- and Diastereoselectivity of Isoxazolidine Formation by Lewis Acids
Eur. J. Org. Chem. 2008, 277 – 284.

S. Yekta, V. Prisyazhnyuk, H.-U. Reißig*
Simple Modifications of Enantiopure 1,2-Oxazines Leading to Building Blocks for Carbohydrate and Peptide Mimetics
Synlett 2007, 2069 – 2072.

E. Schmidt, H.-U. Reißig*, R. Zimmer
Regio- and Stereoselective 1,3-Dipolar Cycloadditions to 6H-1,2-Oxazines Leading to New Heterobicyclic Compounds
Synthesis 2006, 2074 -2084

E. Schmidt, H.-U. Reißig, O. Rademacher*
Crystal Structure of 3aS*,4S*,7aR*-4-Ethoxy-3a,7a-dihydro-3,7-diphenyl-
4H-1,5-dioxa-2,6-diazaindene, C19H18N2O3

Z. Kristallogr. NCS 2000, 215, 283 - 284.

R. Zschiesche, H.-U. Reißig*
Reductive Transformations of Polyfunctional Nitro Compounds: Synthesis of Methyl 7-Aminoalkanoates and Five-Membered Cyclic Nitrones - Inter- and Intramolecular 1,3-Dipolar Cycloadditions
Liebigs Ann. Chem. 1989, 551 - 557.

J. L. Flippen-Anderson, I. Karle, R. Huisgen*, H.-U. Reißig
Trimerisierung eines Azomethin-imins durch drei aufeinanderfolgende 1,3-dipolare Cycloadditionen
Angew. Chem. 1980, 92, 936 - 937.

J. L. Flippen-Anderson, I. Karle, R. Huisgen*, H.-U. Reißig
Trimerization of an Azomethine Imine by Threee Successive 1,3-Dipolar Cycloaddition Reactions
Angew. Chem. Int. Ed. Engl. 1980, 19, 906 - 907.

R. Huisgen*, H.-U. Reißig
Cycloadditions to Methyl 3,3-Dimethyl-3H-pyrazole-5-carboxylate
J. Chem. Soc., Chem. Commun. 1979, 568 - 570.

R. Huisgen*, H.-U. Reißig, H. Huber, S. Voss
α-Diazocarbonyl Compounds and Enamines - A Dichotomy of Reaction Paths
Tetrahedron Lett. 1979, 2987 - 2990.

H.-U. Reißig, R. Huisgen*
Conducted Tour Mechanism of Ester Group Migration in a 3H-Pyrazole
J. Am. Chem. Soc. 1979, 101, 3648 - 3649.

R. Huisgen*, H.-U. Reißig, H. Huber
Diazocarbonyl Compounds and 1-Diethylaminopropyne
J. Am. Chem. Soc. 1979, 101, 3647 - 3648.

W. Bihlmaier, R. Huisgen*, H.-U. Reißig, S. Voss
Reactivity Sequences of Dipolarophiles Towards Diazocarbonyl Compounds - MO Pertubation Treatment
Tetrahedron Lett. 1979, 2621 - 2624.

R. Huisgen*, W. Bihlmaier, H.-U. Reißig
Azokupplung von α-Diazocarbonylverbindungen mit N-(1-Cyclopentenyl)aminen
Angew. Chem. 1979, 91, 347 - 348.

R. Huisgen*, W. Bihlmaier, H.-U. Reißig
Azo Coupling of a-Diazo Cyrbonyl Compounds with N-(1-Cyclopentenyl)amines
Angew. Chem. Int. Ed. Engl. 1979, 18, 331 - 332.

R. Huisgen*, H.-U. Reißig
Cycloadditionen von α-Diazocarbonylverbindungen an Enamine
Angew. Chem. 1979, 91, 346 - 347.

  R. Huisgen*, H.-U. Reißig
Cycloadditions of a-Diazo Carbonyl Compounds to Enamines
Angew. Chem. Int. Ed. Engl. 1979, 18, 330 - 331.

J. Geittner, R. Huisgen*, H.-U. Reißig
Solvent Dependence of Cycloaddition Rates of Phenyldiazomethane and Activation Parameters
Heterocycles (Sendai) 1978, 11, 109 - 112.

L. Fisera, J. Geittner, R. Huisgen*, H.-U. Reißig
Cycloaddition Rates of Diazomethane and Diphenyldiazomethane
Heterocycles (Sendai) 1978, 10, 153 - 158.

W. Bihlmaier, J. Geittner, R. Huisgen*, H.-U. Reißig
The Stereospecificity of Diazomethane Cycloadditions
Heterocycles (Sendai) 1978, 10, 147 - 152.

 

Direct link

 Publications 

H. Angert, R. Czerwonka, H.-U. Reißig*
Mukaiyama Reactions of a Silyl Enol Ether with Heteroatom-Substituted β-Formyl Esters
Liebigs Ann./Recueil 1997, 2215 - 2220.
 
H. Angert, R. Czerwonka, H.-U. Reißig*
TiCl4 and LiClO4 Promoted Additions of O-Silylketene Acetals to Chiral β-Formyl Esters
J. Prakt. Chem. 1997, 339, 453 - 455.
 
H. Angert, R. Schumacher, S. Foro, H.-U. Reißig, H. J. Lindner*
Crystal Structure of 4,5-Dihydro-4,4-dimethyl-5-(4,4-dimethyl-3-oxo-2-pentyl)-
2(3H)-furanone, OCOCH2C(CH3)2CHCH(CH3)COC(CH3)3

Z. Kristallogr. 1996, 211, 403 - 404.
 
H. Angert, R. Schumacher, S. Foro, H.-U. Reißig, H. J. Lindner*
Crystal Structure of 4,5-Dihydro-5-(4,4-dimethyl-3-oxo-2-pentyl)-2(3H)-furanone, OCO(CH2)2CHCH(CH3)COC(CH3)3
Z. Kristallogr. 1996, 211, 401 - 402.
 
H. Angert, R. Schumacher, H.-U. Reißig*
Chelate-Controlled Additions of Titanium and Lithium Enolates to Chiral β-Formyl Esters - Diastereofacial and Simple Diastereoselectivity
Chem. Ber. 1996, 129, 227 - 232.
 
H. Angert, R. Czerwonka, H.-U. Reißig*
Additions of Silyl Enol Ethers to β-Formyl Esters - A Chelate-Controlled Synthesis of the Pheromone (+)-Eldanolide.
Liebigs Ann. 1996, 259 - 263.
 
H.-U. Reißig*, H. Angert, T. Kunz, A. Janowitz, G. Handke, E. Bruce-Adjei
Ester Groups as Effective Ligands in Chelate-Controlled Additions of Cuprates and Grignard Reagents to Chiral β-Formyl Esters
J. Org. Chem. 1993, 58, 6280 - 6285.
 
H. Angert, T. Kunz, H.-U. Reißig*
Chelate-Controlled Mukaiyama Reactions with Chiral β-Formyl Esters
in Tetrahedron-Symposium-in-Print on Organotitanium Reagents in Organic Synthesis (M. T. Reetz, Ed.)
Tetrahedron 1992, 48, 5681 - 5690.
 
T. Kunz, A. Janowitz, H.-U. Reißig*
A Chelate-Controlled Route to Disubstituted and Tetrasubstituted γ-Lactones - Stereoselectivity in Lewis Acid Promoted Additions to Chiral Methyl β-Formylcarboxylates
Chem. Ber. 1989, 122, 2165 - 2175.
 
A. Janowitz, T. Kunz, G. Handke, H.-U. Reißig*
Asymmetric 1,2- and 1,3-Inductions and Solvent Dependence Found in Chelate-Controlled Additions of Grignard Reagents and Cuprates to Chiral β-Formyl Esters – Stereoselective Synthesis of γ-Lactones
Synlett 1989, 24 – 25.

T. Kunz, H.-U. Reißig*
Radical Additions in Aqueous Medium: Direct Synthesis of 5-Allyl-Substituted γ-Lactones from Allylic Bromides/Zinc and Methyl γ-Oxocarboxylates
Liebigs Ann. Chem. 1989, 891 - 893.
 
T. Kunz, H.-U. Reißig*
Ein neuer Weg zu trans-substituierten γ-Lactonen
Angew. Chem. 1988, 100, 297 - 298.

T. Kunz, H.-U. Reißig*
A New Route to trans-Substituted γ-Lactones
Angew. Chem. Int. Ed. Engl. 1988, 27, 268 - 270.

 

Direct link

Publications

D. Reich, D. S. Müller, L. Schefzig, R. Zimmer,* H.-U. Reißig*
One-Pot Generation of C≡X Bonds from Methyl 2-Siloxycyclopropanecarboxylates: Simple Syntheses of Functionalized Nitriles and Alkynes
Synlett 2014, 25, 2265 – 2270.

T. H. Ngo, H. Berndt, D. Lentz, H.-U. Reißig*
Linear and Cyclic Amides with a Thiophene Backbone: Ultrasound-Promoted Synthesis and Crystal Structures
J. Org. Chem. 2012, 77, 9676 – 9683.

D. Gladow, H.-U. Reißig*
Synthesis of Perfluoroalkyl-Substituted γ-Lactones and 4,5-Dihydropyridazin-3(2H)-ones via Donor-Acceptor Cyclopropanes
Helv. Chim. Acta 2012, 95, 1818 1830.

H. Özbek, I. S. Veljkovic, H.-U. Reißig*
Gewald Synthesis of Aminothiophene Carboxylic Acids Providing New Dipeptide Analogues
Synlett 2008, 3145 – 3148.

H.-U. Reißig*, G. Böttcher, R. Zimmer
New 1,3-Dihydroazepin-2-one Derivatives by [3,3]-Sigmatropic Rearrangement of Suitably Substituted 2-Alkenylcyclopropyl Isocyanates
Can. J. Chem 2004, 82, 166 – 176.

H.-U. Reißig*, R. Zimmer
Donor-Acceptor-Substituted Cyclopropane Derivatives and their Application in Organic Synthesis
Chem. Rev. 2003, 103, 1151 – 1196.

P. K. Patra, H.-U. Reißig*
Functionalized Azamacrocycles and Large-Ring α-Amino Esters by One-Pot Syntheses from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
Eur. J. Org. Chem. 2001, 4195 – 4206.

R. Zimmer, A. Ziemer, M. Gruner, I. Brüdgam, H. Hartl, H.-U.  Reißig*
Siloxycyclopropanes in Ugi Four-Component Reaction: A New Method for Synthesis of Highly Substituted Pyrrolidinone Derivatives
Synthesis 2001, 1649 – 1658.

P. K. Patra, H..U. Reißig*
An Efficient One-pot Synthesis of Functionalized Azamacrocycles from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
Synlett 2001, 33 – 36.

F. A. Khan, R. Czerwonka, H.-U. Reißig*
Pd-Catalyzed Reactions of Donor-Acceptor Substituted Cyclopropanes and their Ring-opened Derivatives: Attempted Heck Cyclization and Novel One-pot Enolate Arylations
Eur. J. Org. Chem. 2000, 3607 - 3617.

G. Böttcher, H.-U. Reißig*
Synthesis of New Highly Substituted 1,3-Dihydroazepin-2-ones Starting from 2-Siloxycyclopropanecarboxylates
Synlett 2000, 725 - 727.

D. Sperling, H.-U. Reißig, J. Fabian*
1,3-Sigmatropic Rearrangements of Divinylcyclopropane Derivatives and Hetero Analogs in Competition with Cope-Type Rearrangements - A DFT Study
Eur. J. Org. Chem. 1999, 1107 - 1114.

A. Ullmann, M. Gruner, H.-U. Reißig*
Synthesis of Functionalized Cyclophanes by Ring-Opening/Ring-Closure Cascade Reactions of Siloxycyclopropanes
Chem. Eur. J. 1999, 5, 187 – 197.

A. Ullmann, H.-U. Reißig*, O. Rademacher
A Repetitive Approach to the Synthesis of Medium and Large Ring Compounds with a Ring-Opening/Ring-Closure Cascade Reaction of Siloxycyclopropane Derivatives as Crucial Step
Eur. J. Org. Chem. 1998, 2541 – 2549.

D. Sperling, H.-U. Reißig, J. Fabian*
A DFT Study on the Vinylcyclopropanecarbaldehyde to 2,5-Dihydrooxepin Hetero-Cope-type Rearrangement and on Related Reactions
Liebigs Ann./Recueil 1997, 2443 - 2450.

H.-U. Reißig*, R. Schumacher, D. Ferse
Baeyer-Villiger Oxidations of γ-Oxo Esters - Determination of the Absolute Configurations of Methyl 2-Siloxycyclopropanecarboxylates - Interpretation of the Enantioselective Cyclopropanations of Silyl Enol Ethers
Liebigs Ann./Recueil 1997, 2119 - 2124.

D. Sperling, H.-U. Reißig, J. Fabian*
Quantenchemische Berechnungen zur chemischen Reaktivität: Isomerisierung einiger substituierter Cyclopropane
Wiss. Z. Techn. Univ. Dresden 1997, 46, (Heft 5) 33 - 38.

R. Schumacher, F. Dammast, H.-U. Reißig*
Screening of Various Catalysts for the Asymmetric Cyclopropanation of Structurally Typical Silyl Enol Ethers - Scope and Limitations of Evans's Bisoxazoline Copper Catalyst
Chem. Eur. J. 1997, 3, 614 - 619.

R. Schumacher, H.-U. Reißig*
Influence of Nucleophilicity of Silyl Enol Ethers on Stereoselectivities in Asymmetric Cyclopropanation Reactions
Liebigs Ann./Recueil 1997, 521 - 526.

R. Schumacher, H.-U. Reißig*
Stereoselective Cyclopropanation of Chiral Carbohydrate-Derived Enol Ethers
Synlett 1996, 1121 - 1122.

M. Buchert, H.-U. Reißig*
Rearrangement of Donor-Acceptor-Substituted Vinylcyclopropanes to Functionalized Cyclopentene Derivatives: Evidence for Zwitterionic Intermediates
Liebigs Ann. 1996, 2007 - 2013.

F. A. Khan, R. Czerwonka, H.-U. Reißig*
A Novel Pd(0)-Catalyzed One-Pot Transformation of Substituted Siloxycyclopropanes to Indane Derivatives
Synlett 1996, 533 - 535.

J. Schnaubelt, E. Marks, H.-U. Reißig*
[4+1] Cycloadditions of the Rhodium Di(methoxycarbonyl) Carbenoid to 2-Siloxy-1,3-dienes
Chem. Ber. 1996, 129, 73 - 75.

J. Schnaubelt, A. Ullmann, H.-U. Reißig*
An Efficient One-Pot Synthesis of Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes
Synlett 1995, 1223 – 1225.

J. Schnaubelt, H.-U. Reißig*
Chelate Controlled Intramolecular Diels-Alder Reaction as Key for Synthesis of a Dihydromevinolin Precursor
Synlett 1995, 452 - 454.

B. Hofmann, H.-U. Reißig*
Characteristic Reactions of 4-Siloxy-2,5-dihydrooxepines: Desilylation, [2+2] and [4+2] Cycloadditions
Chem. Ber. 1994, 127, 2337 - 2339.

B. Hofmann, H.-U. Reißig*
Swern Oxidation of Alkenyl-Substituted 2-(tert-Butyldimethylsiloxy)-1-
(hydroxymethyl)-cyclopropanes: A Novel and Flexible Route to Functionalized 2,5-Dihydrooxepines

Chem. Ber. 1994, 127, 2327 - 2335.

B. Hofmann, H.-U. Reißig*
Synthesis of New Alkenyl-Substituted 2-(tert-Butyldimethylsiloxy)cyclopropane-
carboxylates and their Diastereoselective Conversion into (Hydroxymethyl)-
cyclopropanes

Chem. Ber. 1994, 127, 2315 - 2325.

K. Paulini, H.-U. Reißig*
Synthesis of Dipeptides Containing Novel Cyclopropyl- and Cyclopropenyl-Substituted β- und γ-Amino Acids
Liebigs Ann. Chem. 1994, 549 – 554.

F. Dammast, H.-U. Reißig*
Synthese optisch aktiver 2-Siloxycyclopropancarbonsäureester durch asymmetrische Katalyse II. Einfluß der Silylenoletherstruktur auf die enantioselektive Cyclopropanierung mit Diazoessigsäuremethylester
Chem. Ber. 1993,126, 2727 - 2732.

F. Dammast, H.-U. Reißig*
Synthese optisch aktiver 2-Siloxycyclopropancarbonsäureester durch asymmetrische Katalyse I. Katalysatoreinfluß auf die Cyclopropanierung von (Z)-1-Phenyl-1-(trimethylsiloxy)prop-1-en
Chem. Ber. 1993, 126, 2449 - 2456.

J. Schnaubelt, R. Zschiesche, H.-U. Reißig*, H. J. Lindner, J. Richter
Synthese von Östronderivaten aus Siloxycyclopropancarbonsäureestern
Liebigs Ann. Chem. 1993, 61 - 70.

B. Hofmann, H.-U. Reißig*
Synthesis of Functionalized 2,5-Dihydrooxepines by [3,3]-Sigmatropic Rearrangement of Cyclopropane Derivatives
Synlett 1993, 27 - 29.

H.-U. Reißig*, I. Reichelt, T. Kunz
Methoxycarbonylmethylation of Aldehydes Via Siloxycyclopropanes: Methyl 3,3-Dimethyl-4-oxobutanoate
Org. Synth. 1992, 71, 189 - 199.

K. Paulini, H.-U. Reißig*
Ein effektiver Weg zu GABA-analogen Aminosäuren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen
Liebigs Ann. Chem. 1991, 455 – 461.

H.-E. Radunz*, H.-U. Reißig, G. Schneider, A. Riethmüller
Synthese enantiomerenreiner γ-Keto-δ-aminosäuren, zentrale Bausteine vieler Enzyminhibitoren
Liebigs Ann. Chem. 1990, 705 - 707.

T. Kunz, A. Janowitz, H.-U. Reißig*
Eine flexible Synthese von 4-Oxobutansäuremethylestern und deren Derivaten
Synthesis 1990, 43 - 47.

Patent:
H.-E. Radunz, H.-U. Reißig
Verfahren zur enantioselektiven Herstellung von γ-Keto-δ-aminosäurederivaten,
Deutsches Patentamt (P 3919898 vom 19.6.1989)

R. Zschiesche, H.-U. Reißig*
Reductive Transformations of Polyfunctional Nitro Compounds: Synthesis of Methyl 7-Aminoalkanoates and Five-Membered Cyclic Nitrones - Inter- and Intramolecular 1,3-Dipolar Cycloadditions
Liebigs Ann. Chem. 1989, 551 - 557.

H.-U. Reißig*, H. Holzinger, G. Glomsda
A Titanoxycyclopropane as Intermediate in a Highly Stereoselective Homoaldol Type Addition - Syntheses of cis-Substituted Tetrahydrofuran Derivatives
Tetrahedron-Symposium-in-Print on Strain-Assisted Synthesis (L. Ghosez, Ed.), Tetrahedron 1989, 45, 3139 - 3150.

T. Kunz, H.-U. Reißig*
Enantioselective Synthesis of Siloxycyclopropanes and of γ-Oxocarboxylates by Asymmetric Catalysis
Tetrahedron Lett. 1989, 30, 2079 - 2082.

H.-U. Reißig*, R. Zschiesche, A. Wienand, M. Buchert
Synthesis with Donor-Acceptor-Substituted Vinylcyclopropanes
in "Strain and Its Implications in Organic Chemistry" (A. de Meijere, S. Blechert, Eds.), S. 51 - 58, Kluwer Academic Publishers, Dordrecht 1989.

R. Zschiesche, T. Hafner, H.-U. Reißig*
Conversion of Polyfunctional Nitroalkanes into Carbonyl Compounds - Synthesis of the Pheromone Chalcogran and of Key Building Blocks for the Macrolides Pyrenophorin and Vermiculine
Liebigs Ann. Chem. 1988, 1169 - 1173.

R. Zschiesche, H.-U. Reißig*
Efficient Syntheses of Polyfunctional Nitro Compounds Using 2-Alkenyl-Substituted Methyl 2-Siloxycyclopropanecarboxylates as Key Building Blocks
Liebigs Ann. Chem. 1988, 1165 - 1168.

C. Brückner, H. Holzinger, H.-U. Reißig*
Diastereoselective Syntheses of Highly Substituted Methyl Tetrahydrofuran-3-carboxylates by Reactions of γ-Lactols with Silylated Nucleophiles
J. Org. Chem. 1988, 53, 2450 – 2456.

C. Brückner, H.-U. Reißig*
Efficient and Flexible Syntheses of Paraconic Esters and Other Highly Substituted Furanone Derivatives from Methyl 2-Siloxycyclopropanecarboxylates
J. Org. Chem. 1988, 53, 2440 - 2450.

C. Brückner, B. Suchland, H.-U. Reißig*
Eine neue Synthese von Pyrrolderivaten
Liebigs Ann. Chem. 1988, 471 - 473.

C. Brückner, H.-U. Reißig*
Thiophenderivate aus 2-Siloxycyclopropancarbonsäureestern durch neuartige 1,3- und 1,2-sigmatrope Umlagerungen
Liebigs Ann. Chem. 1988, 465 - 470.

H.-U. Reißig
Donor-Acceptor-Substituted Cyclopropanes: Versatile Building Blocks in Organic Synthesis
Top. Curr. Chem. 1988, 144, 73 - 135.

R. Zschiesche, H.-U. Reißig*
An Efficient Synthesis of 5-Membered Cyclic Nitrones from γ-Nitro Ketones
Tetrahedron Lett. 1988, 29, 1685 - 1686.

R. Zschiesche, H.-U. Reißig*
Eine Synthese von rac-Norbisabolid
Liebigs Ann. Chem. 1987, 387 - 388.

C. Brückner, H.-U. Reißig*
Geschwindigkeit und Regioselektivität der Hydrogenolyse einiger phenylsubstituierter Cyclopropane
Chem. Ber. 1987, 120, 627 - 629.

C. Brückner, H.-U. Reißig*
Katalytische Hydrogenolyse von 2-Siloxycyclopropancarbonsäureestern: Untersuchungen zu Chemo-, Regio- und Stereoselektivität
Chem. Ber. 1987, 120, 617 - 626.

W. Bretsch, H.-U. Reißig*
Synthese von β,γ-ungesättigten Ketonen und γ-Hydroxycarbonylverbindungen aus 2-Siloxycyclopropancarbonsäuremethylestern
Liebigs Ann. Chem. 1987, 175 - 178.

R. Zschiesche, E. L. Grimm, H.-U. Reißig*
Intramolekulare Diels-Alder-Reaktionen mit 2-Trimethylsiloxy-2-vinylcyclopropancarbonsäureestern als Schlüsselbausteinen
Angew. Chem. 1986, 98, 1104 - 1105; Angew. Chem. Int. Ed. Engl. 1986, 25, 1086 - 1087.

H.-U. Reißig*, I. Reichelt, H. Lorey
C-C-Verknüpfung durch Lewis-Säure-induzierte Cyclopropanringspaltung - Neue Wege zu hochsubstituierten Furan(on)derivaten
Liebigs Ann. Chem. 1986, 1924 - 1939.

H.-U. Reißig*, H. Lorey
Selenylierung, Sulfenylierung und Aminomethylierung von 2-Siloxycyclopropancarbonsäureestern durch Lewis-Säure-induzierte Ringöffnung
Liebigs Ann. Chem. 1986, 1914 - 1923.

C. Brückner, H. Lorey, H.-U. Reißig*
Diastereoselektive Synthese funktionalisierter Tetrahydrofuran-Derivate aus γ-Lactolen
Angew. Chem. 1986, 98, 559 – 560.

C. Brückner, H. Lorey, H.-U. Reißig*
Diastereoselektive Synthesis of Funktionalized Tetrahydrofuran Derivates from γ-Lactols
Angew. Chem. Int. Ed. Engl. 1986, 25, 556 - 557.

H.-U. Reißig*, H. Lorey
Lewis Acid promoted Additions of Cyclopropanes to Iminium Salts: A New Possibility for α-Methylene-γ-butyrolactone Synthesis
J. Chem. Soc., Chem. Commun. 1986, 269 - 271.

E. L. Grimm, R. Zschiesche, H.-U. Reißig*
2-Alkenyl-Substituted Methyl 2-Siloxycyclopropanecarboxylates as Masked Vinyl Ketones: Efficient Syntheses of Highly Functionalized Michael Adducts
J. Org. Chem. 1985, 50, 5543 - 5545.

C. Brückner, H.-U. Reißig*
Synthesis of Functionalized Furan Derivatives by Hydroxyalkylation of Methyl 2-Siloxycyclopropanecarboxylates
J. Chem. Soc., Chem. Commun. 1985, 1512 - 1513.

H.-U. Reißig
A Novel Rearrangement Leading to Methoxycarbonylmethylated Silyl Enol Ethers
Tetrahedron Lett. 1985, 26, 3943 - 3946.

C. Brückner, H.-U. Reißig*
Thiophenderivate durch neue Umlagerungen siloxysubstituierter Cyclopropancarbonsäureester
Angew. Chem. 1985, 97, 578 - 579.

C. Brückner, H.-U. Reißig*
Thiophene Derivatives by Novel Rearrangements of Siloxy-substituted Cyclopropanecarboxylates
Angew. Chem. Int. Ed. Engl. 1985, 24, 588 - 589.

I. Reichelt, H.-U. Reißig*
Neue Chrysanthemumsäurederivative durch Deprotonierung-Alkylierung
Liebigs. Ann. Chem. 1985, 650 - 652.

E. L. Grimm, H.-U. Reißig*
2-Siloxy-Substituted Methyl Cyclopropanecarboxylates as Building Blocks in Synthesis: Efficient One-Pot Conversion to γ-Butyrolactones
J. Org. Chem. 1985, 50, 242 - 244.

H.-U. Reißig*, I. Reichelt
Ring Cleaving Selenenylation and Sulfenylation of Cyclopropane Derivatives Promoted by TiCl4
Tetrahedron Lett. 1984, 25, 5879 - 5880.

I. Reichelt, H.-U. Reißig*
Eine einfache und flexible Synthese für 4,5-Dihydro-2H-3-pyridazinone
Synthesis 1984, 786 - 787.

I. Reichelt, H.-U. Reißig*
Zur Ringöffnung von 2-(Trimethylsilylmethyl)cyclopropancarbonsäuremethylester
Liebigs Ann. Chem. 1984, 828 - 830.

I. Reichelt, H.-U. Reißig*
Flexible und effektive Synthese für 4-Oxo-2-alkensäuremethylester
Liebigs Ann. Chem. 1984, 820 - 827.

E. Kunkel, I. Reichelt, H.-U. Reißig*
Ringöffnungsreaktionen von 2-Siloxycyclopropancarbonsäuremethylestern zu 4-Oxoalkansäurederivaten
Liebigs Ann. Chem. 1984, 802 - 819.

I. Reichelt, H.-U. Reißig*
Deprotonierung und diastereoselektive Alkylierung von 2-siloxysubstituierten Cyclopropancarbonsäuremethylestern
Liebigs Ann. Chem. 1984, 531 - 551.

E. Kunkel, I. Reichelt, H.-U. Reißig*
Synthese von 2-siloxysubstituierten Cyclopropancarbonsäuremethylestern
Liebigs Ann. Chem. 1984, 512 - 530.

I. Reichelt, H.-U. Reißig
Deprotonierung und diastereoselektive Alkylierung von Cyclopropancarbonsäuremethylestern
Chem. Ber. 1983, 116, 3895 - 3914.

H.-U. Reißig*, I. Böhm
Low Temperature Equilibration of Cyclopropanes by Lewis Acid Catalysis
Tetrahedron Lett. 1983, 24, 715 - 718.

I. Böhm, R. Schulz, H.-U. Reißig*
An Efficient and Highly Flexible Synthesis of α,β-Unsaturated γ-Oxoesters
Tetrahedron Lett. 1982, 23, 2013 - 2016.

H.-U. Reißig*, I. Böhm
High Diastereoselection in the Alkylation of Siloxy-Substituted Methyl Cyclopropanecarboxylates - Consequence of a Pyramidal Ester Enolate Anion?
J. Am. Chem. Soc. 1982, 104, 1735 - 1737.

H.-U. Reißig
Lewis-Acid-Promoted Additions of Carbonyl Compounds to Donor-Acceptor Substituted Cyclopropanes: A New Synthesis of 2,3-Dihydrofuran Derivatives
Tetrahedron Lett. 1981, 22, 2981 - 2984.

I. Böhm, E. Hirsch, H.-U. Reißig*
Alkylierung von Donor-Acceptor-substituierten Cyclopropanen: ein flexibler Weg zu 4-Oxocarbonsäureestern
Angew. Chem. 1981, 93, 593 - 594.

I. Böhm, E. Hirsch, H.-U. Reißig*
Alkylation of Donor-Acceptor Substituted Cyclopropanes: A Flexible Route to 4-Oxocarboxylic Acid Esters
Angew. Chem. Int. Ed. Engl. 1981, 20, 574.

H.-U. Reißig*, E. Hirsch
Donor-acceptor-substituierte Cyclopropane: Synthese und Ringöffnung zu 1,4-Di-carbonylverbindungen
Angew. Chem. 1980, 92, 839 - 840.

H.-U. Reißig*, E. Hirsch
Donor-Acceptor-Substituted Cyclopropanes: Synthesis und Ring Opening to 1,4-Dicarbonyl Compounds
Angew. Chem. Int. Ed. Engl. 1980, 19, 813 - 814.

 

Direct link

Publications 

M. Hoffmann, M. Buchert, H.-U. Reißig*
Reactions of Fischer Carbene Complexes with Siloxydienes: Formation of Cycloheptadiene and Cyclopentene Derivatives - Formal [2+1] Cycloaddition Followed by Cope Rearrangement Versus Formal [3+2] Cycloaddition with or without Preceding Carbene-Ligand Metathesis
Chem. Eur. J. 1999, 5, 876 - 882.

M. Hoffmann, M. Buchert, H.-U. Reißig*
Weitere Überraschungen mit Fischer-Carbenkomplexen: formale [3+2]-Cycloadditionen mit und ohne vorgeschalteter Carbenligandmetathese
Angew. Chem. 1997, 109, 281 - 283.

M. Hoffmann, M. Buchert, H.-U. Reißig*
New Surprises with Fischer Carbene Complexes: Formal [3+2]Cycloadditions with and without Preceding Carabene-Ligand Metathesis
Angew. Chem. Int. Ed. 1997, 36, 283 – 285.

M. Buchert, H.-U. Reißig*
Rearrangement of Donor-Acceptor-Substituted Vinylcyclopropanes to Functionalized Cyclopentene Derivatives: Evidence for Zwitterionic Intermediates
Liebigs Ann. 1996, 2007 - 2013.

M. Hoffmann, H.-U. Reißig*
A Unique Solvent Effect Governing Periselectivity of the Carbene Transfer from Fischer Carbene Complexes: Mechanism, Scope and Limitation of Their Formal [3+2] Cycloaddition to Electron-Deficient Olefins
Synlett 1995, 625 - 627.

M. Buchert, M. Hoffmann, H.-U. Reißig*
On the Regioselectivity and Stereoselectivity of the Carbene Transfer from Fischer Carbene Complexes to Trisubstituted Electron-Deficient 1,3-Dienes
Chem. Ber. 1995, 128, 605 - 614.

M. Buchert, H.-U. Reißig*
Highly Functionalized Vinylcyclopropane Derivatives by Regioselective and Stereoselective Reactions of Fischer Carbene Complexes with 1,4-Disubstituted Electron-Deficient 1,3-Dienes
Chem. Ber. 1992, 125, 2723 - 2729.

A. Wienand, H.-U. Reißig*, H. Fischer*, D. Pflumm, C. Troll
Synthese und Kristallstrukturanalyse von Alkinylcarbenkomplexverbrückten Dicobalthexacarbonylkomplexen
J. Organomet. Chem. 1992, 427, C9 - C14.
 
A. Wienand, H.-U. Reißig*
Zur Bildung von Vinylcyclopropan- und Cyclopentenderivaten aus alkenylsubstituierten Chromcarben-Komplexen: Konkurrenz von formalen [2+1]- und [3+2]-Cycloadditionen
Chem. Ber. 1991, 124, 957 - 965.
 
A. Wienand, H.-U. Reißig*
Reactions of Fischer Carbene Complexes with Electron-Deficient Olefins: Scope and Limitations of This Route to Donor-Acceptor-Substituted Cyclopropanes
Organometallics 1990, 9, 3133 - 3142.

A. Wienand, H.-U. Reißig*
Stereospezifische Insertion des Carbenliganden eines Fischer-Carbenkomplexes in olefinische C-H-Bindungen
Angew. Chem. 1990, 102, 1156 - 1157.

A. Wienand, H.-U. Reißig*
Stereospezific Insertion of the Carbene Ligand of a Fischer Carbene Complex into Olefinic C–H Bonds
Angew. Chem. Int. Ed. Engl. 1990, 29, 1129 - 1131.
 
A. Wienand, H.-U. Reißig*, H. Fischer, J. Hofmann
Eine einfache Synthese neuartiger alkenylsubstituierter Chromcarben-Komplexe
Chem. Ber. 1989, 122, 1589 - 1592.

H.-U. Reißig
Donor-Acceptor-Substituted Cyclopropanes via Fischer Carbene Complexes
in "Organometallics in Organic Synthesis" (H. Werner, G. Erker, Eds.), S. 311 - 322, Springer, Heidelberg 1989.

A. Wienand, M. Buchert, B. Hofmann, H.-U. Reißig*
The Carbene Complex Route to Donor-Acceptor-Substituted Cyclopropanes
in "Advances in Metal Carbene Chemistry" (U. Schubert, Ed.) S. 271 - 273, Kluwer Academic Publishers, Dordrecht 1989.

M. Buchert, H.-U. Reißig*
Regioselective and Stereoselective Synthesis of Vinylcyclopropane Derivatives from 1,3-Dienes and a Fischer Carbene Complex
Tetrahedron Lett. 1988, 29, 2319 - 2320.

A. Wienand, H.-U. Reißig*
The Carbene Complex Route to Donor-Acceptor-Substituted Cyclopropanes
Tetrahedron Lett. 1988, 29, 2315 - 2318.

 

Direct link

Publications

•  M. S. Andrä, J. Thiemermann, J. Schnaubelt, D. Lentz, R. Zimmer, H.-U. Reißig*
TADDOL-Promoted Enantioselective Intramolecular Diels-Alder Reactions of 1,7,9-Decatrien-3-ones to Octalin Derivatives
Eur. J. Org. Chem. 2017, 124 – 130.

•  J. Thiemermann, J. Schnaubelt, R. Zimmer, H.-U. Reißig*
Diastereoselective Diels-Alder Reactions of 1,7,9-Decatrien-3-ones to Highly Substituted Octalin Derivatives
Synthesis 2016, 48, 5712 – 5715.

•  J. Thiemermann, M. S. Andrä, J. Schnaubelt, D. Lentz, R. Zimmer, H.-U. Reißig*
A Modular Four-Component Route to Substituted 1,7,9-Decatrien-3-ones Using a Chloro-Substituted Phosphorane as Key C3 Building Block
Synthesis 2016, 48, 4081 – 4090.

B. Frey, H.-U. Reißig*
Facile Synthesis of an Octahydrobenzocycloheptenone Derivative Utilising Intramolecular Diels-Alder Reaction
J. Prakt. Chem. 1999, 341, 173 - 178.
 
J. Schnaubelt, B. Frey, H.-U. Reißig*
Formal Total Synthesis of (+)-Dihydromevinolin via a Chelate-Controlled Intramolecular Diels-Alder Reaction as the Key Step
Helv. Chim. Acta 1999, 82, 666 - 676.
 
B. Frey, J. Schnaubelt, H.-U. Reißig*
Variable Stereocontrol in Cycloadditions of 1,7,9-Decatrien-3-ones by Different Lewis Acidic Promoters - Application to a Short Synthesis of α-Eudesmol
Eur. J. Org. Chem. 1999, 1385 - 1393.
 
B. Frey, J. Schnaubelt, H.-U. Reißig*
Studies on the Synthesis of Natural Products with Bicyclo[4.4.0]decene Skeleton: Synthesis and Uncatalysed Intramolecular Diels-Alder Reactions of the Decatrienone Substrates
Eur. J. Org Chem. 1999, 1377 - 1384.
 
J. Schnaubelt, H.-U. Reißig*
Chelate Controlled Intramolecular Diels-Alder Reaction as Key for Synthesis of a Dihydromevinolin Precursor
Synlett 1995, 452 - 454.
 
B. Frey, S. Hünig*, M. Koch, H.-U. Reißig*
Seven-Membered Ring Chelates as a Tool for Stereocontrol in Intramolecular Diels-Alder Reactions: Application to a Short Synthesis of α-Eudesmol
Synlett 1991, 854 - 856.
 
R. Zschiesche, B. Frey, E. Grimm, H.-U. Reißig*
Zur Stereoselektivität der intramolekularen Diels-Alder-Reaktionen von 1,7,9-Decatrien-3-onen zu Octalonderivaten
Chem. Ber. 1990, 123, 363 - 374.
 
R. Zschiesche, E. L. Grimm, H.-U. Reißig*
Intramolekulare Diels-Alder-Reaktionen mit 2-Trimethylsiloxy-2-vinylcyclopropancarbonsäureestern als Schlüsselbausteinen
Angew. Chem. 1986, 98, 1104 - 1105.

R. Zschiesche, E. L. Grimm, H.-U. Reißig*
Intramolecular Diels-Alder-Reactions with Methyl 2-Trimethylsiloxy-2-vinylcyclopropanecarboxylates as Key Building Blocks
Angew. Chem. Int. Ed. Engl. 1986, 25, 1086 - 1087.

 

Direct link

Publications

K. Paulini, H.-U. Reißig*, P. Rademacher
On the Reactivity of N,N-Bis(trimethyl)silylated Enamines: Model Studies on Hetero Diels-Alder Reactions and Other Cycloadditions
J. Prakt. Chem. 1995, 337, 209 - 215.

K. Paulini, A. Gerold, H.-U. Reißig*
Reactions of 6-[Bis(trimethylsilyl)amino]-5,6-dihydro-4H-1,2-oxazines
Liebigs Ann. 1995, 667 - 671.

K. Paulini, H.-U. Reißig*
Preparation of Novel Lipophilic GABA-Analogues Containing Cyclopropane Rings via Cyclopropanation of N-Silylated Unsaturated Amines
J. Prakt. Chem. 1995, 337, 55 - 59.

K. Paulini, H.-U. Reißig, J. Richter, H. J. Lindner*, H. Paulus
Crystal Structure of c-6-[N,N-Bis(trimethylsilyl)amino]-5,6-dihydro-
r-4-[(1'-hydroxy-1'-methyl)ethyl]-t-5-methyl-3-phenyl-4H-1,2-oxazine,
ONC(CH)(CH)(CH)(C6H5)-C(OH)(CH3)2(CH3)NSi(CH3)3Si(CH3)3

Z. Kristallogr. 1994, 209, 900 - 901.

K. Paulini, H.-U. Reißig*
Synthesis of Dipeptides Containing Novel Cyclopropyl- and Cyclopropenyl-Substituted β- und γ-Amino Acids
Liebigs Ann. Chem. 1994, 549 - 554.

K. Paulini, H.-U. Reißig*
Diastereoselective Radical Bromination of 5,6-Dihydro-4H-1,2-oxazines and Subsequent Substitution Reactions with Nitrogen Nucleophiles
Chem. Ber. 1994, 127, 685 - 689.

A. G. Beck-Sickinger*, E. Hoffmann, K. Paulini, H.-U. Reißig, K.-D. Willim, H. A. Wieland, G. Jung
High-Affinity Analogues of Neuropeptide Y Containing Conformationally Restricted Non-Proteinogenic Amino Acids
Biochem. Soc. Trans. 1994, 22, 145 - 149.

K. Paulini, H.-U. Reißig*
N-Silylation: New Possibilities for Long-Known Amines
in "Organosilicon Chemistry: From Molecules to Materials" (N. Auner, J. Weis, Eds.), S. 65 - 66, VCH Verlagsgesellschaft 1994.

W. Adam, M. Ahrweiler, K. Paulini, H.-U. Reißig, V. Voerckel*
Dimethyldioxirane Oxidation of Enamines: First Spectral Evidence for Enamine Oxides by Stabilization through N-Silylation
Chem. Ber. 1992, 125, 2719 - 2722.

K. Paulini, H.-U. Reißig*
Efficient Synthesis of a Novel GABA Analogue Incorporating a Cyclopropene Ring
Synlett 1992, 505 - 506.

K. Paulini, H.-U. Reißig*
Ein effektiver Weg zu GABA-analogen Aminosäuren: Cyclopropanierung von N-silylierten Allylaminen und Enaminen
Liebigs Ann. Chem. 1991, 455 - 461.

 

Direct link

 Publications 

A  Hölemann, H.-U. Reißig*
Synthesis of New Furan Derivatives and 4-Hydroxy Aldehydes from 4-Hydroxy 1-Enol Ethers
Synthesis 2004, 1963 – 1970.

A. Schmitt, H.-U. Reißig*
Synthesis of 2-(Phenylselanyl)tetrahydrofurans from γ-Lactones and of γ-Hydroxydiselenoacetals from γ-Lactols
Synthesis 2001, 867 - 870.
 
A. Schmitt, H.-U. Reißig*
Lewis Acid Promoted Reactions of γ-Lactols with Silyl Enol Ethers - Stereoselective Formation of Functionalized Tetrahydrofuran Derivatives
Eur. J. Org. Chem. 2001, 1169 - 1174.
 
A. Schmitt, H.-U. Reißig*
On the Stereoselectivity of γ-Lactol Substitutions with Allyl- and Propargylsilanes - Synthesis of Disubstituted Tetrahydrofuran Derivatives
Eur. J. Org. Chem. 2000, 3893 - 3901.
 
A. Schmitt, H.-U. Reißig*
Stereoselective Substitution at Phenyl-Substituted γ-Lactols with Organometallic Compounds
Chem. Ber. 1995, 128, 871 - 876.
 
A. Schmitt, H.-U. Reißig*
A Highly Diastereoselective Route to Disubstituted Tetrahydrofuran Derivatives by Substitution of γ-Lactols with Silylated Nucleophiles
Synlett 1990, 40 - 42.
 
H.-U. Reißig*, H. Holzinger, G. Glomsda
A Titanoxycyclopropane as Intermediate in a Highly Stereoselective Homoaldol Type Addition - Syntheses of cis-Substituted Tetrahydrofuran Derivatives
Tetrahedron-Symposium-in-Print on Strain-Assisted Synthesis (L. Ghosez, Ed.),
Tetrahedron 1989, 45, 3139 - 3150.
 
C. Brückner, H. Holzinger, H.-U. Reißig*
Diastereoselective Syntheses of Highly Substituted Methyl Tetrahydrofuran-3-carboxylates by Reactions of γ-Lactols with Silylated Nucleophiles
J. Org. Chem. 1988, 53, 2450 - 2456.
 
C. Brückner, H. Lorey, H.-U. Reißig*
Diastereoselektive Synthese funktionalisierter Tetrahydrofuran-Derivate aus γ-Lactolen
Angew. Chem. 1986, 98, 559 - 560; Angew. Chem. Int. Ed. Engl. 1986, 25, 556 - 557.

 

Direct link

Publications

P. K. Patra, H.-U. Reißig*
Functionalized Azamacrocycles and Large-Ring α-Amino Esters by One-Pot Syntheses from Methyl 2-Siloxy-2-vinylcyclopropanecarboxylates
Eur. J. Org. Chem. 2001, 4195 – 4206.

P. K. Patra, H.-U. Reißig*
An Efficient One-pot Synthesis of Functionalized Azamacrocycles from Methyl 2-Siloxy-2-vinylcyclopropane Carboxylates
Synlett 2001, 33 - 36.
 
A. Ullmann, G. Zahn*, J. Schnaubelt, H.-U. Reißig
Crystal Structure of Trimethyl 3-methyl-4-oxo-(E)-8-cyclodecene-1,1,6-
tricarboxylate, C17H24O7

Z. Kristallogr. NCS 1999, 214, 221 - 223.
 
A. Ullmann, M. Gruner, H.-U. Reißig*
Synthesis of Functionalized Cyclophanes by Ring-Opening/Ring-Closure Cascade Reactions of Siloxycyclopropanes
Chem. Eur. J. 1999, 5, 187 - 197.
 
A. Ullmann, H.-U. Reißig*, O. Rademacher
A Repetitive Approach to the Synthesis of Medium and Large Ring Compounds with a Ring-Opening/Ring-Closure Cascade Reaction of Siloxycyclopropane Derivatives as Crucial Step
Eur. J. Org. Chem. 1998, 2541 - 2549.
 
A. Ullmann, J. Schnaubelt, H.-U. Reißig* (Feature Article)
Synthesis of Highly Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes: Scope and Limitations
Synthesis 1998, 1052 - 1066.
 
J. Schnaubelt, A. Ullmann, H.-U. Reißig*
An Efficient One-Pot Synthesis of Functionalized Cyclodecenone Derivatives from Siloxycyclopropanes
Synlett 1995, 1223 - 1225.
Direct link

Publications 

•  H.-U. Reißig, R. Zimmer
Nitrosoalkenes
in Science of Synthesis (Knowledge Update) 2015/2, Thieme Verlag, Stuttgart, 315 – 334.

N. Moinizadeh, R. Klemme, M. Kansy, R. Zimmer,* H.-U. Reißig*
Convenient Syntheses of Enantiopure 1,2-Oxazin-4-yl Nonaflates and Phosphates and Their Palladium-Catalyzed Cross-Couplings
Synthesis 2013, 45, 2752 – 2762.

I. Linder, M. Gerhard, L. Schefzig, M. Andrä, C. Bentz, H.-U. Reißig,* R. Zimmer
A Modular Synthesis of Functionalized Pyridines through Lewis-Acid-Mediated and Microwave-Assisted Cycloadditions between Azapyrylium Intermediates and Alkynes
Eur. J. Org. Chem. 2011, 6070 – 6078.

R. Zimmer, M. Buchholz, M. Collas, J. Angermann, K. Homann, H.-U. Reißig*
1,2-Oxazines as Building Blocks for Stereoselective Synthesis: Preparation of Oxygen-Substituted 1,2-Oxazines, either by Alcohol Addition or by Epoxidation, and Subsequent Hydrogenation Leading to 1,2-Amino Alcohols and Pyrrolidines
Eur. J. Org. Chem. 2010, 4111 – 4122.

R. Zimmer, E. Schmidt, M. Andrä, M.-A. Duhs, I. Linder, H.-U. Reißig*
Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines
Beilstein Journal of Organic Chemistry 2009, 5, No. 44.

R. Zimmer, M. Collas, R. Czerwonka, U. Hain, H.-U. Reißig*
A New Access to Pyrrolizidine Derivatives: Ring Contraction of Methyl (E)-[1,2-Oxazin-3-yl]propenoates
Synthesis 2008, 237 – 244.

H.-U. Reißig*, K. Homann, F. Hiller, R. Zimmer
A Stereoselective Access to Dihydroxylated Pyrrolidines by Reductive Ring Contraction of 1,2-Oxazines.
Synthesis, 2007,  2681 – 2689.

H.-U. Reißig, R. Zimmer*
1-Nitrosoalkenes
in: Science of Synthesis, 2006, Vol. 33, 371 – 389.

E. Schmidt, H.-U. Reißig*, R. Zimmer
Regio- and Stereoselective 1,3-Dipolar Cycloadditions to 6H-1,2-Oxazines Leading to New Heterobicyclic Compounds
Synthesis 2006, 2074 - 2084.

M. Buchholz, H.-U. Reißig*
Enantioselective Syntheses of the Pyrrolidine Core of Endothelin Antagonist ABT-627 (Atrasentan) via 1,2-Oxazines
Eur. J. Org. Chem. 2003, 3524 - 3533.

R. Zimmer, B. Orschel, S. Scherer, H.-U. Reißig*
Hetero Diels-Alder Reactions of Nitroso Alkenes with Alkoxyallene Derivatives Bearing Carbohydrate Auxiliaries - Asymmetric Synthesis of 6H-1,2-Oxazines and Subsequent Reductive Transformations
Synthesis 2002, 1553 - 1563.
 
M. Buchholz, F. Hiller, H.-U. Reißig*
Synthesis of Enantioenriched 2-Substituted 4-Phenylbutylamines by Hydrogenolysis of Optically Pure 6-Alkoxy-5,6-dihydro-4H-1,2-oxazines
Eur. J. Org. Chem. 2002, 2838 - 2843.

M. Buchholz, H.-U. Reißig*
Highly Stereoselective and Flexible Synthesis of 6-Alkoxy-5,6-dihydro-4H-1,2-oxazines by Conjugate Addition of Organolithium Compounds to 6H-1,2-Oxazines Followed by Trapping with Electrophiles
Synthesis 2002, 1412 - 1422.

A. A. Tishkov, H.-U. Reißig*, S. Ioffe
Preparation of Cyclic and Bicyclic γ-Amino Acid Derivatives from Methyl 6-Ethoxy-5,6-dihydro-4H-1,2-oxazine-4-carboxylate
Synlett 2002, 863 - 866.

H. Hartl*, I Brüdgam, H.-U. Reißig, M. Buchholz
Crystal Structure of (4S*,5R*,6S*)-6-Ethoxy-4-(1R*)-(1-hydroxy-1-
phenyl)methyl-3,5-diphenyl-5,6-dihydro-4H-1,2-oxazine, C25H25NO3
Z. Kristallogr. NCS 2001, 216, 591 – 592.

E. Schmidt, H.-U. Reißig, O. Rademacher*
Crystal structure of 3aS*,4S*,7aR*-4-ethoxy-3a,7a-dihydro-3,7-diphenyl-4H-1,5-
dioxa-2,6-diaza-indene, C19H18N2O3

Z. Kristallogr. NCS 2000, 215, 283 - 284.

R. Zimmer, K. Homann, J. Angermann, H.-U. Reißig*
Stereoselective Preparation of 4,5-Dihydroxy-5,6-dihydro-4H-1,2-oxazines and Their Derivatives
Synthesis 1999, 1223 - 1235.
 
D. Sperling, H.-U. Reißig, J. Fabian*
1,3-Sigmatropic Rearrangements of Divinylcyclopropane Derivatives and Hetero Analogs in Competition with Cope-Type Rearrangements – A DFT Study
Eur. J. Org. Chem. 1999, 1107 – 1114.

R. Zimmer, F. Hiller, H.-U. Reißig*
1,4-Addition of Organolithium Compounds to 6-Ethoxy-3-phenyl-6H-1,2-oxazine
Heterocycles 1999, 50, 393 - 401.
 
K. Homann, J. Angermann, M. Collas, R. Zimmer, H.-U. Reißig*
Synthesis of 6-Ethoxy-6H-1,2-oxazines by Hetero Diels-Alder Reaction of 1-Bromo-2-ethoxyethene with α-Nitroso Alkenes
J. Prakt. Chem. 1998, 340, 649 – 655.
 
U. Jänicke-Rößler, G. Zahn*, F. Hiller, H.-U. Reißig
Crystal structure of (6S)-6-[(1R,2S,5R)-(–)-2-Ιsopropyl-5-methylcyclo-
hexyloxy]-3-phenyl-6H-1,2-oxazine, [ONC(CH)3(C6H5)O(CH)2(CH2)2CHCH2CH(CH3)2CH3]

Z. Kristallogr. 1998, 213, 261 - 262.
 
R. Zimmer, J. Angermann, U. Hain, F. Hiller, H.-U. Reißig*
Hetero Diels-Alder Reactions of 2-Chloro-1-nitroso-1-phenylethene: Preparation of Novel 4-Chloro-Substituted 1,2-Oxazines and Subsequent Reactions
Synthesis 1997, 1467 - 1474.
 
D. Sperling, A. Mehlhorn, H.-U. Reißig, J. Fabian*
Theoretical Study of Pericyclic Reactions of Nitrosoethylene and (Thionitroso)ethylene
Liebigs Ann. 1996, 1615 - 1621.
 
R. Zimmer, H.-U. Reißig*
Lithiated 3-trifluoromethyl-substituted 1,2-Oxazines and their Reactions
J. Fluorine Chem. 1996, 80, 21 - 26.
 
R. Zimmer, H.-U. Reißig*, K. Homann
1,2-Azapyrylium Ions: Properties and Synthetic Applications
J. Prakt. Chem. 1995, 337, 521 - 528.
 
J. Angermann, K. Homann, H.-U. Reißig*, R. Zimmer
Synthesis and cis-Dihydroxylation of 6H-1,2-Oxazines - Synthesis of Dihydroxyprolinols
Synlett 1995, 1014 - 1016.
 
K. Paulini, H.-U. Reißig*, P. Rademacher
On the Reactivity of N,N-Bis(trimethyl)silylated Enamines: Model Studies on Hetero Diels-Alder Reactions and Other Cycloadditions
J. Prakt. Chem. 1995, 337, 209 - 215.
 
K. Homann, R. Zimmer, H.-U. Reißig*
Reactions of Azapyrylium Ions with Nucleophiles: From Crazy Products to a Novel Pyridine Synthesis
Heterocycles 1995, 40, 531 - 537.
 
K. Paulini, A. Gerold, H.-U. Reißig*
Reactions of 6-[Bis(trimethylsilyl)amino]-5,6-dihydro-4H-1,2-oxazines
Liebigs Ann. 1995, 667 - 671.
 
T. Arnold, H.-U. Reißig, J. Richter, H. J. Lindner*, H. Paulus
Crystal structure of 3-O-(5,6-dihydro-5-methyl-3-phenyl-4H-1,2-oxazin-6-yl)
-1,2:5,6-di-O-isopropyliden-α-D-glucofuranose,
O(CH)4OCO(CH3)2CHCH2OCO(CH3)2OCHCHCH2CNO(CH3)(C6H5)

Z. Kristallogr. 1994, 209, 903 - 904.
 
K. Homann, H.-U. Reißig, S. Foro, H. J. Lindner*
Crystal structure of 2-methyl-6-phenyl-pyridin-3-al, (C6H5)C(CH)2CCNCHO(CH3)
Z. Kristallogr. 1994, 209, 902.

R. Zimmer, T. Arnold, K. Homann, H.-U. Reißig*
An Efficient and Simple Synthesis of 3,4,5,6-Tetrahydro-2H-1,2-oxazines by Sodium Cyanoborohydride Reduction of 5,6-Dihydro-4H-1,2-oxazines
Synthesis 1994, 1050 - 1056.
 
K. Paulini, H.-U. Reißig*
Diastereoselective Radical Bromination of 5,6-Dihydro-4H-1,2-oxazines and Subsequent Substitution Reactions with Nitrogen Nucleophiles
Chem. Ber. 1994, 127, 685 - 689.
 
R. Zimmer*, K. Homann, H.-U. Reißig*
Reductive Transformations of 6H-1,2-Oxazines with Hydride Reagents: Formation of Aziridines and 3-Hydroxyalkylated 1,2-Oxazines
Liebigs Ann. Chem. 1993, 1155 - 1157.
 
R. Zimmer, M. Hoffmann, H.-U. Reißig*
Model Studies of the Reduction of 3-Phenyl-6H-1,2-oxazines, Chemo- and Stereoselectivity: Synthesis of Amino Alcohols, Amino Acids, and Related Compounds
Chem. Ber. 1992, 125, 2243 - 2248.
 
T. Arnold, B. Orschel, H.-U. Reißig*
Diacetonglucose als Hilfsgruppe bei der asymmetrischen Hetero-Diels-Alder-Reaktion mit Nitrosoalkenen
Angew. Chem. 1992, 104, 1084 - 1086.
 
T. Arnold, B. Orschel, H.-U. Reißig*
Diacetoneglucose as Auxiliary Group for the Asymmetric Hetero-Diels-Alder Reaction with Nitrosoalkenes
Angew. Chem. Int. Ed. Engl. 1992, 31, 1033 - 1035.

R. Zimmer*, M. Collas, M. Roth, H.-U. Reißig
6-Siloxy-Substituted 5,6-Dihydro-4H-1,2-oxazines as Key Building Blocks for Natural Products
Liebigs Ann. Chem. 1992, 709 - 714.
 
R. Zimmer, H.-U. Reißig*, H.J. Lindner
Unerwartete Bildung von β-Lactamen aus 6H-1,2-Oxazinen unter Lewis-Säure-Einwirkung
Liebigs Ann. Chem. 1992, 621 - 624.
 
R. Zimmer, H.-U. Reißig*
Efficient Synthesis of Trifluoromethyl-Substituted 5,6-Dihydro-4H-1,2-oxazines by the Hetero-Diels-Alder Reaction of 1,1,1-Trifluoro-2-nitroso-2-propene and Electron-Rich Olefins
J. Org. Chem. 1992, 57, 339 - 347.
 
C. Unger, R. Zimmer, H.-U. Reißig*, E.-U. Würthwein
Deprotonation of 5,6-Dihydro-5-methylene-4H-1,2-oxazines and Regioselective Reactions with Electrophiles
Chem. Ber. 1991, 124, 2279 - 2287.
 
R. Zimmer, H.-U. Reißig*
Synthesis of 6H-1,2-Oxazines by Hetero Diels-Alder Reactions of Nitroso Alkenes towards Methoxyallenes
Liebigs Ann. Chem. 1991, 553 - 562.
 
H.-U. Reißig*, C. Hippeli
Lithiated 5,6-Dihydro-4H-1,2-oxazines: Synthesis, Highly Diastereoselective Reactions with Electrophiles, and Subsequent Transformations
Chem. Ber. 1991, 124, 115 - 127.
 
H.-U. Reißig*, C. Hippeli, T. Arnold
On the Mechanism of Diels-Alder Reactions of Nitroso Alkenes: Exo/Endo-Selectivity, Stereospecificity, E/Z-Selectivity, and Relative Reactivity of Various Olefins
Chem. Ber. 1990, 123, 2403 - 2411.
 
T. Arnold, H.-U. Reißig*
Hetero Diels-Alder Reactions of Optically Active Enol Ethers with a Nitroso Alkene: Asymmetric Synthesis of 1,2-Oxazine Derivatives
Synlett 1990, 514 - 516.
 
C. Hippeli, H.-U. Reißig*
Reductive Transformations of 5,6-Dihydro-4H-1,2-oxazines: Synthesis of 4-Hydroxy Ketoximes, N-Hydroxypyrrolidine Derivatives, and Other Nitrogen Containing Compounds
Liebigs Ann. Chem. 1990, 475 - 481.
 
C. Hippeli, R. Zimmer, H.-U. Reißig*
Transition Metal and Acid-Induced Transformations of 6-Siloxy-Substituted
5,6-Dihydro-4H-1,2-oxazines: Preparation of Pyrroles, Nitrones, 1,4-Dicarbonyl Compounds and Derivatives Thereof

Liebigs Ann. Chem. 1990, 469 - 474.
 
C. Hippeli, H.-U. Reißig*
Synthesis of Trialkylsiloxy-Substituted and Other 5,6-Dihydro-4H-1,2-oxazines by Hetero Diels-Alder Reactions of Nitroso Alkenes - Preparative Scope and Diastereoselectivity
Liebigs Ann. Chem. 1990, 217 - 226.
 
C. Hippeli, N. Basso, F. Dammast, H.-U. Reißig*
A Practical Method for the Separation of E/Z-Isomeric Silyl Enol Ethers by Kinetic Resolution
Synthesis 1990, 26 – 27.

R. Zimmer, H.-U. Reißig*
Nucleophile Substitution an 6H-1,2-Oxazinen über Azapyrylium-Ionen
Synthesis 1989, 908 - 911.
 
R. Zimmer, H.-U. Reißig*
Methoxyallene als Komponenten in Diels-Alder-Reaktionen mit inversem Elektronenbedarf: Synthese von 6H-1,2-Oxazinen
Angew. Chem. 1988, 100, 1576 - 1577.
 
R. Zimmer, H.-U. Reißig*
Methoxyallenes as Components in Diels-Alder Reactions with Inverse Electron Demand: Synthesis of 6H-1,2-Oxazines
Angew. Chem. Int. Ed. Engl. 1988, 27, 1518 - 1519.

C. Hippeli, H.-U. Reißig*
Highly Diastereoselective Deprotonation and Substitution of Chiral 5,6-Dihydro-4H-1,2-oxazines
J. Org. Chem. 1988, 53, 3884 - 3886.
 
C. Hippeli, H.-U. Reißig*
Efficient Synthesis of 6-Trimethylsiloxy- and 6-(Trimethylsilyl)methyl-3-phenyl-
5,6-dihydro-4H-1,2-oxazines by Cycloaddition of α-Nitrosostyrene to Silyl Enol Ethers and Allyltrimethylsilane

Synthesis 1987, 77 - 79.
Direct link

 Publications 

M. Höltje, A. Richartz, B. Zdrazil, A. Schwanke, B. Dugovič, C. Murruzzu, H.-U. Reißig, H. C. Korting, B. Kleuser, H.-D. Höltje, M. Schäfer-Korting*
Human Polymerase α-Inhibitors for Skin Tumors. Part 2. Modeling, Synthesis and Influence on Normal and Transformed Keratinocytes of New Thymidine and Purine Derivatives
J. Enzym. Inhib. Med. Chem., 2010, 25 (2), 250-265.

R. Zimmer,* V. Dekaris, M. Knauer, L. Schefzig, H.-U. Reißig
Synthesis of Poly(Ethylene Glycol)-Supported (R)-BINOL Derivatives and Their First Application in Enantioselective Mukaiyama Aldol Reactions
Synth. Commun. 2009, 1012 – 1026.

R. Zimmer*, L. Schefzig, A. Peritz, V. Dekaris, H.-U. Reißig
Functionalized BINOL Derivatives as Ligands for Enantioselectively Catalyzed Aldol Additions: Highly Enantioselective Synthesis of Chiral β-Hydroxy Thioesters
Synthesis 2004, 1439 – 1445.

R. Zimmer*, A. Peritz, R. Czerwonka, L. Schefzig, H.-U. Reißig
Optimisation, Scope and Limitations of Enantioselective Aldol Reactions of an S-Ketene Silyl Acetal with Aliphatic Aldehydes under (R)-BINOL-Titanium(IV) Catalysis Conditions
Eur. J. Org. Chem. 2002, 3419 – 3428.

M. Hölzer, W. Burd, H.-U. Reißig, K.-H. van Pée*
Substrate Specificity and Regioselectivity of Tryptophan 7-Halogenase from Pseudomonas fluoreszens BL915
Adv. Synth. Catal. 2001, 343, 591 – 595.

R. Zimmer*, U. Hain, M. Berndt, R. Gewald, H.-U. Reißig
Enantioselective Synthesis of (S)- and (R)-6-Hydroxy-8-nonenecarboxylates by Asymmetric Catalysis: A Formal Synthesis of (R)-α-Lipoic Acid and its (S)-Antipode
Tetrahedron: Asymmetry 2000, 11, 879 - 887.

H. Scheytza, H.-U. Reißig, O. Rademacher*, F. Hahn, J. Richter
Crystal Structure of 5,13,20,27-Tetraazonia-32-thiaheptacycloy
[25.2.2.22,5.213,16.217,20.17,11.122,25]-nonatriaconta-
2,4,7,9,11(37),13,15,17,19,22,24,27,29,30,33,35,38-heptadecaene Tetrakis(hexafluorophosphate),
C34H30F24N4P4S

Z. Kristallogr. NCS 2000, 215, 75 - 76.

H. Scheytza*, O. Rademacher, H.-U. Reißig
Synthesis and Structures of Novel Pyridine-Bridged Phanes of 4,4'-Bipyridine
Eur. J. Org. Chem. 1999, 2373 - 2381.

H. Scheytza*, H.-U. Reißig, O. Rademacher
Novel Furan-, Thiophene- and Benzo[b]thiophene Bridged Macrocycles of 4,4'-Bipyridine
Tetrahedron 1999, 55, 4709 - 4720.

H. Scheytza*, H.-U. Reißig
Unexpected Decomposition of a Monoquarternated 4,4'-Bipyridinium Dication by Disodium Dithionite Reduction in Water
Tetrahedron 1999, 55, 1057 - 1062.

R. Zimmer, H.-U. Reißig*
Reaction of Cyclooctyne with Fischer Carbene Complexes - Synthesis of Tricyclic Quinone Derivatives
J. Prakt. Chem. 1998, 340, 755 - 756.

H. Scheytza*, H.-U. Reißig
Cyclo(paraquat-o-phenylene-paraquat-p-phenylene) - The Missing Isomeric Carbophane of 4,4'-Bipyridine
Tetrahedron Lett. 1998, 39, 8637 - 8640.

W. Adam*, D. Reinhardt, H.-U. Reißig, K. Paulini
Epoxidation of Vinylamides by Dimethyldioxirane: First Spectral Evidence for Enamide Oxides
Tetrahedron 1995, 51, 12257 - 12262.

T. Hafner, H.-U. Reißig*
(S)-5-Nitro-2-pentanol durch Reduktion mit Bäckerhefe
Liebigs Ann. Chem. 1989, 937 – 938.

R. Zschiesche, H.-U. Reißig*
An Efficient Synthesis of 5-Membered Cyclic Nitrones from γ-Nitro Ketones
Tetrahedron Lett. 1988, 29, 1685 – 1686.

E. Piers*, M.S. Burmeister, H.-U. Reißig
Thermal Rearrangement of Functionalized 1,2-Divinylcyclopropane Systems. A Convenient Synthesis of Substituted 4-Cyclohepten-1-ones
Can. J. Chem. 1986, 64, 180 – 187.

H. Bader, H.-U. Reißig*
The First 4-Dialkylamino-1,2-dihydropyridine Derivatives: Synthesis and Basic Reactions
Tetrahedron 1986, 42, 835 – 838.

M. Horner, S. Hünig*, H.-U. Reißig
Reversible Umwandlung eines [4]-Radialens in ein Cyclobutadien durch vierstufige Elektronenübertragung
Liebigs Ann. Chem. 1983, 658 – 667.

E. Hirsch, S. Hünig*, H.-U. Reißig
Darstellung von (2,2-Dimethyl-1-methylenpropyl)methansulfonat und -trifluoracetat
Chem. Ber. 1982, 115, 399 – 401.

R. Knorr*, E. Lattke, F. Ruf, H.-U. Reißig
Vinyl-to-Benzyl Isomerization and Electrocyclizations in Lithio Derivatives of o-Tolylstilbenes
Chem. Ber. 1981, 114, 1592 – 1599.

H.-U. Reißig*, B. Scherer
A Simple Synthesis of Thiol Esters from Copper-I-Mercaptides and Acyl Chlorides
Tetrahedron Lett. 1980, 21, 4259 – 4262.

E. Piers*, H.-U. Reißig
Synthese von cis-2-Vinylcyclopropylketonen: neue Synthese von 4-Cycloheptenonen
Angew. Chem. 1979, 91, 857 – 858.

E. Piers*, H.-U. Reißig
Synthesis of cis-2-Vinylcyclopropyl Ketones: a New Synthesis of 4-Cycloheptenones
Angew. Chem. Int. Ed. Engl. 1979, 18, 791 – 792.

 

Direct link