An Asymmetric Total Synthesis of D-Homo Steroids Involving a Lewis Acid Directed Diels-Alder Reaction-Reference-Cited by-同舟云学术

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An Asymmetric Total Synthesis of D-Homo Steroids Involving a Lewis Acid Directed Diels-Alder Reaction

Published:1978-01 Issue:7 Volume:8 Page:427-436
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Cohen Noal,Banner Bruce L.,Eichel Wayne F.,Valenta Zdenek,Dickinson Robert A.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397917808063570

Reference20 articles.

1. Asymmetric synthesis of bicyclic intermediates of natural product chemistry

2. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures

3. Asymmetric induction in 19-norsteroid total synthesis

4. Totalsynthese von (+)-D-Homoöstron-3-methyläther

5. A facile approach to an optically active tetracyclic intermediate for the synthesis of 6-methyl-19-norsteroids

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3. The Diels–Alder Reaction in Steroid Synthesis;Synthesis;2014-11-17

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