An improved procedure for the lipase-catalysed kinetic resolution of endo-endo-cis-bicyclo[3.3.0]octane-2,6-diol—synthesis of potential C2-symmetric enantiomerically pure bidentate auxiliaries-Reference-Cited by-同舟云学术

An improved procedure for the lipase-catalysed kinetic resolution of endo-endo-cis-bicyclo[3.3.0]octane-2,6-diol—synthesis of potential C2-symmetric enantiomerically pure bidentate auxiliaries

Published:1997-06 Issue:12 Volume:8 Page:2051-2055
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Lemke Karin,Ballschuh Sibylle,Kunath Annamarie,Theil Fritz

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference17 articles.

1. Enzymes in organic synthesis. Part 3. Synthesis of enantiomerically pure prostaglandin intermediates by enzyme-catalyzed transesterification of (1SR,2RS,5SR,6RS)-bicyclo[3.3.0]octane-2,6-diol with trichloroethyl acetate in an organic solvent

2. Synthesis of (R,R) and (S,S) bicyclo[3.3.0]octane-2,6-dione interactions between non-conjugated chromophores

3. C2 symmetry and asymmetric induction

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