Biomimetic Diastereoselective Total Synthesis of epi-Illudol via a Transannular Radical Cyclizations Strategy-Reference-Cited by-同舟云学术

Biomimetic Diastereoselective Total Synthesis of epi-Illudol via a Transannular Radical Cyclizations Strategy

Published:1997-04-01 Issue:14 Volume:119 Page:3427-3428
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rychlet Elliott Maryse¹,Dhimane Anne-Lise¹,Malacria Max¹

Affiliation:

1. Université Pierre et Marie Curie, Paris VI Laboratoire de Chimie Organique de Synthèse associé au CNRS, Tour 44-54, B. 229, 4, Place Jussieu 75252 - Paris, Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja970139i

Reference34 articles.

1. Sesquiterpene alcohols with novel skeletons from the fungus (ascomycotina)

2. Structure of the major metabolite of 1-allyl-3,5-diethyl-6-chlorouracil — new bicyclic barbituric acid derivatives

3. Synthesis of (.+-.)-illudol

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