On the tendency of 1,2,3,6-tetrahydrobenzocyclobutene-3,6-diones for undergoing site-selective Diels-Alder reactions at the internal double bond
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Site-selective Diels-Alder reactions of 1,4,5,8-naphthodiquinones with anthracenes and successively with cyclopentadiene: electronic effects vs. steric effects
2. Synthetic routes to benz[f]indenes
3. Linear annelation of tricyclic quinones by site selective reaction with dienes.
4. DIELS–ALDER REACTIONS OF 1,2,3,6-TETRAHYDROBENZOCYCLOBUTENE-3,6-DIONES. A NEW SYNTHESIS OF [4.4.2]PROPELLANES AND A DIVERGENCE OF SITESELECTIVITY CONTROLLED BY STERIC HINDRANCE
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1. Spontaneous Dimerization of Allenes in Situ: An Efficient Synthesis of Substituted 1,2-Dimethylenecyclobutanes with High Regio- and Stereoselectivities;Chemistry - A European Journal;2015-08-21
2. Intermolecular Cyclization Reactions to form Carbocycles;PATAI'S Chemistry of Functional Groups;2009-12-15
3. Synthesis, electrochemistry and ab initio molecular orbital calculations on some norbornane- and bicyclo[2.2.2]octane-fused 5,12-bis(dicyanomethylidene)naphthalene systems;Journal of the Chemical Society, Perkin Transactions 2;1996
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