Synthesis and thermal rearrangement of a potential butalene-anthracene adduct
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1,4-benzenediyl structure
2. Generation and trapping of butalene
3. Further evidence for the formation of butalene in the reaction of 1-chloro-[2.2.0]bicyclohexa-2,5-dienes[dewar chlorobenzenes] with a strong base
4. See, for example, P. Ashkenazi, J. Oliker and D. Ginsberg, references cited there, and earlier papers in this series;
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1. A comparative investigation of 1,4-pentamethylene and 1,4-hexamethylene Dewar benzene: Evidence for the intermediate formation of [5]paracyclophane;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Eliminations Involving Carbon-Halogen Bonds and Leading to Highly Strained Rings;PATAI'S Chemistry of Functional Groups;2009-12-15
3. The Retro-Diels-Alder Reaction Part I. CC Dienophiles;Organic Reactions;1998-03-23
4. Synthese von triafulvalen-vorstufen durch ‘carben-dimerisierung’ von 1-halogeno-1-lithiocyclopropanen;Helvetica Chimica Acta;1997-11-03
5. 9,10-Dehydroanthracene: p-Benzyne-Type Biradicals Abstract Hydrogen Unusually Slowly;Journal of the American Chemical Society;1996-01-01
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