Dimerisation des polyphenyl-allenes-II
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference42 articles.
1. Dimerisation des polyphenyl-allenes—I
2. Tetramethyleneethanes. Preparation and reactions of a stereochemically labeled precursor
3. The mechanism of allene cycloaddition. III. Thermal and photochemical generation of 2,2'-bis(1,1-dimethylallyl) biradical from an azocyclane precursor
4. Hydrocarbon thermal degenerate rearrangements. V. Stereochemistry of the 1,2-dimethylenecyclobutane self-interconversion and its relation to the allene dimerization and the rearrangements of other C6H8 isomers
5. Hydrocarbon degenerate thermal rearrangements. A reinterpretation of the data and proposed mechanism for the (Z)-2-methylethylidenecyclobutane self-interconversion. Stereochemistry of cyclobutane ring openings
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3. From [10]Paracyclophane to Ferrocenophanones: The Search for Molecular Machines and Bio-Organometallic Anticancer Drugs;Israel Journal of Chemistry;2011-11-07
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