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Synthesis 2012; 44(24): 3789-3796
DOI: 10.1055/s-0032-1317524
DOI: 10.1055/s-0032-1317524
paper
Enantioselective Synthesis of Axially Chiral Tetrasubstituted Allenes via Lipase-Catalyzed Desymmetrization
Weitere Informationen
Publikationsverlauf
Received: 05. August 2012
Accepted after revision: 12. Oktober 2012
Publikationsdatum:
25. Oktober 2012 (online)


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.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information