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Publications of the Reissig Group 2005

272. R. Zimmer*, H.-U. Reißig
1-Methoxyallenyllithium
in: Electronic Encyclopedia of Reagents for Organic Synthesis
John Wiley & Sons, Chichester, 2005.
 
271. A. Al-Harrasi, I. Brüdgam, H. Hartl, H.-U. Reißig*
Crystal structure of 1R,5S,8R,9S-8-azidomethyl-2-benzyl-6,6-dimethyl-
3,7-dioxa-2-azabicyclo[3.3.1]nonan-9-0l, C16H22N4O3

Z. Kristallogr. NCS 2005, 220, 599 - 600.
 
270. M. Brasholz*, X. Luan, H.-U. Reißig
Towards the Rubromycins: An Efficient Synthesis of a Suitable Isocoumarin Precursor, its Lactam Analogue, and Palladium-Catalyzed Couplings
Synthesis 2005, 3571 - 3580.
 
269. A. Al-Harrasi, H.-U. Reißig*
Enantiomerenreine Kohlenhydratmimetika durch Lewis-Säure-induzierte Umlagerung von 1,3-dioxolanylsubstitutierten 1,2-Oxazinen
Angew. Chem. 2005, 117, 6383 - 6387.
 
  A. Al-Harrasi, H.-U. Reißig*
Synthesis of Enantiopure Carbohydrate Mimetics by Lewis Acid Catalyzed Rearrangement of 1,3-Dioxolanyl-Substituted 1,2-Oxazines
Angew. Chem. Int. Ed. 2005, 44, 6227  –  6231.

268. A. Al-Harrasi, H.-U. Reißig*
Ring Enlargement of 1,2-Oxazines to Enantiopure 1,2-Oxazepine Derivatives and their Palladium-Catalyzed Couplings
Synlett 2005, 2376 - 2378.
 
267. S. Kaden, M. Brockmann, H.-U. Reißig*
Synthesis of Enantiopure 2-Substituted Pyrrolidin-3-ones via Lithiated Alkoxyallenes - An Auxilary Based Synthesis of Both Enantiomers of the Antibiotic Anisomycin.
Helv. Chim. Acta 2005, 88, 1826 - 1838.
 
266. A. Al-Harrasi, H.-U. Reißig*
Synthesis of Enantiopure Functionalized β-Alkoxy γ-Amino Aldehydes by a New Internal Redox Ring Cleavage of Carbohydrate Derived 1,2-Oxazines
Synlett 2005, 1152 - 1154.
 
265. M. Helms, W. Schade, R. Pulz, T. Watanabe, A. Al-Harrasi, L. Fisera, I. Hlobilová, G. Zahn, H.-U. Reißig*
Stereodivergent Syntheses of Highly Substituted Enantiopure 4-Alkoxy-3,6-dihydro-2H-1,2-oxazines by Addition of Lithiated Alkoxyallenes to Carbohydrate-Derived Aldonitrones
Eur. J. Org. Chem. 2005, 1003 - 1019.
 
264. M. Helms, H.-U. Reißig*
Ozonolyses of Enantiopure 4-Alkoxy-3,6-dihydro-2H-1,2-oxazines: An Expedient Route to Functionalized α-Amino-β-hydroxy Esters
Eur. J. Org. Chem. 2005, 998-1001.