H. Angert, R. Czerwonka, H.-U. Reißig* Mukaiyama Reactions of a Silyl Enol Ether with Heteroatom-Substituted β-Formyl Esters Liebigs Ann./Recueil1997, 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.) Tetrahedron1992, 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 Synlett1989, 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.