OAK

Absolute configurations of isoflavan-4-ol stereoisomers

Metadata Downloads
Abstract
Isoflavan-4-ol has been synthesized quantitatively from the reduction of isoflavone in the presence of Pd/C and ammonium formate under N(2) atmosphere. Isolation of cis- and trans-isomers was achieved by. ash column chromatography and each enantiomer was separated by Sumi-Chiral column chromatography. Absolute configurations of four stereoisomers were determined by circular dichroism spectroscopy. (C) 2008 Elsevier Ltd. All rights reserved.
Author(s)
Won, DonghoShin, Bok-KyuKang, SuilHur, Hor-GilKim, MihyangHan, Jaehong
Issued Date
2008-03
Type
Article
DOI
10.1016/j.bmcl.2008.01.116
URI
https://scholar.gist.ac.kr/handle/local/17441
Publisher
Pergamon Press Ltd.
Citation
Bioorganic and Medicinal Chemistry Letters, v.18, no.6, pp.1952 - 1957
ISSN
0960-894X
Appears in Collections:
Department of Environment and Energy Engineering > 1. Journal Articles
공개 및 라이선스
  • 공개 구분공개
파일 목록
  • 관련 파일이 존재하지 않습니다.

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.