Photoannelations with α-formyl ketones. A facile synthesis of the cis-9,10-dimethyldecalin ring system of the valerane sesquiterpenes-Reference-Cited by-同舟云学术

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Photoannelations with α-formyl ketones. A facile synthesis of the cis-9,10-dimethyldecalin ring system of the valerane sesquiterpenes

Published:1975-01 Issue:46 Volume:16 Page:3969-3972
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Baldwin S.W.,Gawley R.E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Photoannelations with .alpha.-formyl ketones. Enol specificity in the reaction of acyclic .alpha.-formyl ketones with alkenes

2. A method for the stereoselective introduction of angular methyl groups

3. Alkylation of enolate ions generated regiospecifically via organocopper reactions. Synthesis of decalin sesquiterpene valerane and of prostaglandin model systems

4. The stereoselective synthesis of -valeranone

5. Stereospecific introduction of a vicinally functionalized angular methyl group. A synthesis of 1-valeranone

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1. Evolution of an oxidative dearomatization enabled total synthesis of vinigrol;Org. Biomol. Chem.;2014

2. Isopropylidenetriphenylphosphorane;Encyclopedia of Reagents for Organic Synthesis;2013-09-16

3. de Mayo Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15

4. Stereochemistry and Mechanism in the Wittig Reaction;Topics in Stereochemistry;2007-02-26

5. Total Synthesis of Sesquiterpenes, 1970-79;Total Synthesis of Natural Products;2007-02-20

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