1
ChemInform 2009, 40, issue 02 © 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Enantioselective syntheses O 0031 Cu(I)-Catalyzed Stereospecific Coupling Reactions of Enantioenriched α-Stan- nylated Benzyl Carbamates and Their Application. — A series of enantioenriched α-stannylated benzyl carbamates is treated with allyl bromides and acid chlorides to give coupling products with stereospecificities of up to 98%. The intramolecular vari- ant allows the synthesis of enantioenriched indanols and tetralins such as (XIII) and (XIV). — (LANGE, H.; FROEHLICH, R.; HOPPE*, D.; Tetrahedron 64 (2008) 38, 9123-9135; Org.-Chem. Inst., Westfael. Wilhelms Univ., D-48149 Muenster, Germany; Eng.) — Kieslich 02- 025

ChemInform Abstract: Cu(I)-Catalyzed Stereospecific Coupling Reactions of Enantioenriched α-Stannylated Benzyl Carbamates and Their Application

Embed Size (px)

Citation preview

Page 1: ChemInform Abstract: Cu(I)-Catalyzed Stereospecific Coupling Reactions of Enantioenriched α-Stannylated Benzyl Carbamates and Their Application

www.cheminform.wiley-vch.de

Enantioselective synthesesO 0031 Cu(I)-Catalyzed Stereospecific Coupling Reactions of Enantioenriched α-Stan-

nylated Benzyl Carbamates and Their Application. — A series of enantioenriched α-stannylated benzyl carbamates is treated with allyl bromides and acid chlorides to give coupling products with stereospecificities of up to 98%. The intramolecular vari-ant allows the synthesis of enantioenriched indanols and tetralins such as (XIII) and (XIV). — (LANGE, H.; FROEHLICH, R.; HOPPE*, D.; Tetrahedron 64 (2008) 38, 9123-9135; Org.-Chem. Inst., Westfael. Wilhelms Univ., D-48149 Muenster, Germany; Eng.) — Kieslich

02- 025

ChemInform 2009, 40, issue 02 © 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim