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, MJ; CHOI, GB; KIM, JY; KIM, 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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- There are no files associated with this item.
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