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LIPASE-CATALYZED TRANSESTERIFICATION AS A PRACTICAL ROUTE TO HOMOCHIRAL ACYCLIC ANTI-1,2-DIOLS - A NEW SYNTHESIS OF (+)-ENDO-BREVICOMIN AND (-)-ENDO-BREVICOMIN SCIE SCOPUS

Title
LIPASE-CATALYZED TRANSESTERIFICATION AS A PRACTICAL ROUTE TO HOMOCHIRAL ACYCLIC ANTI-1,2-DIOLS - A NEW SYNTHESIS OF (+)-ENDO-BREVICOMIN AND (-)-ENDO-BREVICOMIN
Authors
KIM, MJCHOI, GBKIM, JYKIM, HJ
Date Issued
1995-08-28
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Abstract
Several anti-1,2-diols (2a-g) have been efficiently resolved by using LPS-catalyzed transesterification and the total synthesis of (+)- and (-)-endo-brevicomin (1) has been achieved starting from one (2g) of the resolved diols.
Keywords
ASYMMETRIC DIHYDROXYLATION; OLEFINS
URI
https://oasis.postech.ac.kr/handle/2014.oak/21728
DOI
10.1016/0040-4039(95)01237-C
ISSN
0040-4039
Article Type
Article
Citation
TETRAHEDRON LETTERS, vol. 36, no. 35, page. 6253 - 6256, 1995-08-28
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김만주KIM, MAHN JOO
Dept of Chemistry
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