Transposition thermique de cycloalkylidenecyclobutanones conjuguees et de methylene-1 spiro [3.n] alconones-2. Une nouvelle methode d'expansion de cycle.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Hydrocarbon degenerate thermal rearrangements. III. Characterization of the methylallene dimers. Stereochemistry of the 1,2-dimethylenecyclobutane ring opening
2. Antarafacial allylic participation in a thermal 1,3-sigmatropic carbon migration
3. Thermal rearrangements of methylenecyclobutanes. Degenerate rearrangement of (Z)-1-ethylidene-2-methylcyclobutane with antarafacial allylic participation
4. Thermal rearrangements of methylenecyclobutanes. Degenerate rearrangement of optically active 1-(Z)-(1-deuterioethylidene)-2-methyl-trans-3,4,4-trideuteriocyclobutane
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1. Intramolecular formal [4+2] cycloaddition of 3-ethoxycyclobutanones and alkenes;Chemical Communications;2010
2. Thermal rearrangement of halogenated dimethylenecyclobutane and methylenecyclobutene derivatives;Tetrahedron Letters;1996-07
3. One or More CH, CC, and/or CC Bonds Formed by Rearrangement;Comprehensive Organic Functional Group Transformations;1995
4. References to Volume 1;Comprehensive Organic Functional Group Transformations;1995
5. Efficient synthesis of 2-vinylcyclobutanones by the rearrangement of 1-methoxy-1-cyclopropylcarbinols under neutral conditions;Tetrahedron;1989-01
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