Concise Approach to (ent )-14 β-Hydroxysteroids through Highly Diastereo-/Enantioselective Diels-Alder Reactions-Reference-Cited by-同舟云学术

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Concise Approach to (ent )-14 β-Hydroxysteroids through Highly Diastereo-/Enantioselective Diels-Alder Reactions

Published:2016-06-27 Issue:31 Volume:22 Page:10808-10812
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Peter Clovis¹,Ressault Blandine¹,Geoffroy Philippe¹,Miesch Michel¹

Affiliation:

1. Université de Strasbourg; Institut de Chimie - UMR 7177; 1 rue Blaise Pascal BP296/R8-67008 Strasbourg Cedex France

Funder

CNRS

Université de Strasbourg

ANR Sterob

Région Alsace

MRT

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference65 articles.

1. Chemical Synthesis of the Cardiotonic Steroid Glycosides and Related Natural Products

2. Steroid reactions and partial synthesis

3. The Total Synthesis of a Natural Cardenolide: (+)-Digitoxigenin

4. Enantioselective total synthesis of (+)-digitoxigenin

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diastereo–/Enantioselective Diels–Alder Synthesis of 14β-Hydroxysteroid Scaffolds: A Combined Experimental and DFT Study;HETEROCYCLES;2019

2. Pot Economy in the Total Synthesis of Estradiol Methyl Ether by Using an Organocatalyst;Angewandte Chemie International Edition;2017-08-21

3. Pot Economy in the Total Synthesis of Estradiol Methyl Ether by Using an Organocatalyst;Angewandte Chemie;2017-08-21

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