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
Citation
Mj. Kim et al., LIPASE-CATALYZED TRANSESTERIFICATION AS A PRACTICAL ROUTE TO HOMOCHIRAL ACYCLIC ANTI-1,2-DIOLS - A NEW SYNTHESIS OF (-ENDO-BREVICOMIN AND (-)-ENDO-BREVICOMIN()), Tetrahedron letters, 36(35), 1995, pp. 6253-6256
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
35
Year of publication
1995
Pages
6253 - 6256
Database
ISI
SICI code
0040-4039(1995)36:35<6253:LTAAPR>2.0.ZU;2-M
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 th e resolved diols.