Facile synthesis of both linear and angular triquinanes from the tricyclo[5.4.0.01,5]undec-9-ene-8,11-dione efficiently produced by a combination of electro- and photochemical reactions-Reference-Cited by-同舟云学术

Facile synthesis of both linear and angular triquinanes from the tricyclo[5.4.0.01,5]undec-9-ene-8,11-dione efficiently produced by a combination of electro- and photochemical reactions

Published:1994-07 Issue:27 Volume:35 Page:4817-4818
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Maki Shojiro,Toyoda Kunihiro,Mori Takeshi,Kosemura Seiji,Yamamura Shosuke

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference4 articles.

1. Natural products syntheses using anodic oxidation of phenols as a key step

2. Facile synthesis of tricyclo[5.4.0.01,5]undec-9-ene-8,11-diones from phenols with an olefin bearing an electron-attracting group at the side chain

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1. ChemInform Abstract: Facile Synthesis of Both Linear and Angular Triquinanes from Tricyclo( 5.4.0.01,5)undec-9-ene-8,11-dione (I) Efficiently Produced by a Combination of Electro- and Photochemical Reactions.;ChemInform;2010-08-18

2. Oxidation of Phenols;PATAI'S Chemistry of Functional Groups;2009-12-15

3. Asymmetric Photoreactions of Conjugated Enones and Esters;Advances in Photochemistry;2007-01-05

4. Tandem radical rearrangement/Pd-catalysed translocation of bicyclo[2.2.2]lactones. An efficient access to the oxa-triquinane core structure;Organic & Biomolecular Chemistry;2006

5. Chemical and Electrochemical Oxidative Activation of Arenol Derivatives for Carbon-Carbon Bond Formation;Current Organic Chemistry;2004-01-01