Intramolecular cycloaddition/cycloreversion of (E)-3β,17β-diacetoxy-5,10-secoandrost-1(10)-en-5-one-Reference-Cited by-同舟云学术

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Intramolecular cycloaddition/cycloreversion of (E)-3β,17β-diacetoxy-5,10-secoandrost-1(10)-en-5-one

Published:2006-09 Issue:38 Volume:47 Page:6715-6718
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Khripach Vladimir A.,Zhabinskii Vladimir N.,Kuchto Anna I.,Zhiburtovich Yuliya Y.,Gromak Vladimir V.,Groen Marinus B.,van der Louw Jaap,de Groot Aede

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Isolation and structure elucidation of new radical oxidation products of 5-hydroxy steroids

2. Synthesis, Structure, and Reactivity of Secosteroids Containing a Medium-Sized Ring. Part 36. Transannular photocyclization of some unsaturated 5,10-secosteroidal ketones: A reevaluation

3. Structure–reactivity relationships in normal and 19-nor-5,10-seco-steroidal cyclodecenone systems. Part 1. Acid-catalyzed and thermal reactions

4. Configuration and reactivity of ten-membered 5,10-seco-compounds obtained by fragmentation of 5-hydroxy-steroids

5. Conformations of the ten-membered ring in 5,10-secosteroids I. X-ray and NMR. Analysis of (E)-3 ?-hydroxy-5,10-seco-1(10)-cholesten-5-one esters

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