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Asymmetric total synthesis of caribenol A.

A unified strategy is described for the asymmetric total synthesis of caribenol A, which has featured intramolecular Diels-Alder (IMDA) and biomimetic oxidation reactions as key steps.

Journal Title: Journal of the American Chemical Society October 6, 2010, Vol.132(39), pp.13608-13609
Main Author: Liu, Lian-Zhu
Other Authors: Han, Jin-Chun , Yue, Guo-Zong , Li, Chuang-Chuang , Yang, Zhen
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1520-5126 ; DOI: 1520-5126 ; DOI: 10.1021/ja106585n
Link: http://search.proquest.com/docview/756297713/?pq-origsite=primo
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recordid: proquest756297713
title: Asymmetric total synthesis of caribenol A.
format: Article
creator:
  • Liu, Lian-Zhu
  • Han, Jin-Chun
  • Yue, Guo-Zong
  • Li, Chuang-Chuang
  • Yang, Zhen
subjects:
  • Anti-Bacterial Agents–Chemical Synthesis
  • Crystallography, X-Ray–Chemistry
  • Diterpenes–Chemical Synthesis
  • Models, Molecular–Chemistry
  • Molecular Conformation–Chemistry
  • Stereoisomerism–Chemistry
  • Anti-Bacterial Agents
  • Diterpenes
  • Caribenol A
ispartof: Journal of the American Chemical Society, October 6, 2010, Vol.132(39), pp.13608-13609
description: A unified strategy is described for the asymmetric total synthesis of caribenol A, which has featured intramolecular Diels-Alder (IMDA) and biomimetic oxidation reactions as key steps.
language: eng
source:
identifier: E-ISSN: 1520-5126 ; DOI: 1520-5126 ; DOI: 10.1021/ja106585n
fulltext: fulltext
issn:
  • 15205126
  • 1520-5126
url: Link


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