Stereochemistry in the Conversion of Phenyldiazomethane into Stilbenes and Spirooxetanes Caused by Tetrahalogenated 1,4-Benzoquinones. Effects of Halogen Substituents
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/63/2/63_2_630/_pdf
Reference11 articles.
1. Oxidation of organic compounds with cerium(IV). XIII. Cerium(IV)-catalyzed decomposition of aryldiazomethanes to cis- and trans-stilbenes
2. Stereochemistry of the copper perchlorate or copper bromide-catalyzed decomposition of aryldiazomethanes to stilbenes
3. Rhodium ion catalyzed decomposition of aryldiazoalkanes
4. Formation and reactions of aryldiazomethane radical cations
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1. Tetrafluoro-p-benzoquinone;Encyclopedia of Reagents for Organic Synthesis;2005-10-15
2. Formation of Fluorinated 1-Oxaspiro[2.5]octa-4,7-dienes from Polyfluorinated Cyclohexa-2,5-dienones with Diazomethane and Reactions with Aryl and2-Chloroethyl Isocyanates;European Journal of Organic Chemistry;2005-03
3. Cyclohexadienone Ketals and Quinols: Four Building Blocks Potentially Useful for Enantioselective Synthesis;Chemical Reviews;2004-03-01
4. Reactions of polyfluorinated cyclohexadienones with diazoalkanes. Part 1. Formation of cyclopropanes from polyfluorinated cyclohexa-2,4-dienones with diazomethane and phenyldiazomethane;Journal of the Chemical Society, Perkin Transactions 1;2000
5. Reaction of 2,3-Dichloro-5,6-dicyano-p-benzoquinone with 1,10-Phenanthroline and the Crystal Structure of Its Reaction Product;Bulletin of the Chemical Society of Japan;1993-05
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