Photoaddition with 1,2-bis(trimethylsiloxy)cyclobutene: a versatile entry to the stereocontrolled total synthesis of various sesquiterpenes and diterpenes-Reference-Cited by-同舟云学术

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Photoaddition with 1,2-bis(trimethylsiloxy)cyclobutene: a versatile entry to the stereocontrolled total synthesis of various sesquiterpenes and diterpenes

Published:1985-02 Issue:2 Volume:28 Page:165-174
ISSN:0047-2670
Container-title:Journal of Photochemistry
language:en
Short-container-title:Journal of Photochemistry

Author:

de Keukeleire Denis,van Audenhove Martine,van Hijfte Luc,Audenaert Frans,Vandewalle Maurits

Publisher

Elsevier BV

Subject

General Physics and Astronomy,General Chemical Engineering,General Chemistry

Reference26 articles.

1. Total synthesis of polycarbocyclic sesquiterpenes

2. Regio- and stereo-selectivity in [π2 +π2] photocycloaddition reactions between cyclopent-2-enone and electron-rich alkenes

3. The acyloin condensation. III. The synthesis of four-membered rings

4. Die Umsetzung von Carbonsäureestern mit Natrium in Gegenwart von Trimethylchlorsilan

5. A Novel Entry to Substituted Hydroazulenes

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3. Oxonitriles: A Grignard Addition−Acylation Route to Enamides;Organic Letters;2006-09-23

4. A 2-Pyridone Photo-[4 + 4] Approach to the Taxanes;Journal of the American Chemical Society;1996-01-01

5. Enone Olefin [2 + 2] Photochemical Cycloadditions;Organic Reactions;1993-09-29

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