Cycloetherification of hydroxyoleanenes by N-bromosuccinimide.

Abstract:

:Treatment of 28-hydroxyolean-12-enes with N-bromosuccinimide (NBS) in acetonitrile at room temperature afforded 12 alpha-bromooleanan-13beta, 28-epoxides in high yield. This reaction resulted in the formation of olean-9 (11), 12-diene-18alpha, 29-epoxides from 29-hydroxy isomers but recovered only starting materials from 30-hydroxy isomers. NBS will be used a reagent for diagnostic tool to distinguish between isomers bearing a primary hydroxyl group on D/E rings of olean-12-enes.

journal_name

Planta Med

journal_title

Planta medica

authors

Woo WS,Kang SS,Jew SS

doi

10.1055/s-2007-969575

subject

Has Abstract

pub_date

1985-12-01 00:00:00

pages

501-4

issue

6

eissn

0032-0943

issn

1439-0221

journal_volume

51

pub_type

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