Synthesis 2012; 44(24): 3789-3796
DOI: 10.1055/s-0032-1317524
paper
© Georg Thieme Verlag Stuttgart · New York

Enantioselective Synthesis of Axially Chiral Tetrasubstituted Allenes via Lipase-Catalyzed Desymmetrization

Matthias Hammel
Department für Chemie, Universität zu Köln, 50939 Cologne, Germany   Fax: +49(221)4705102   eMail: jan.deska@uni-koeln.de
,
Jan Deska*
Department für Chemie, Universität zu Köln, 50939 Cologne, Germany   Fax: +49(221)4705102   eMail: jan.deska@uni-koeln.de
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Publikationsverlauf

Received: 05. August 2012

Accepted after revision: 12. Oktober 2012

Publikationsdatum:
25. Oktober 2012 (online)


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Abstract

Lipase from Pseudomonas fluorescens efficiently catalyzes the transesterification of prochiral tetrasubstituted allenic diols yielding highly enantioenriched axially chiral allenyl monoesters. In combination with subsequent 5-endo-trig cyclizations geminally disubstituted dihydrofurans are accessible in high optical purity.

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