Photochemistry of novel azabicyclic compounds; concerning the site- and regio-selectivity of di-π-methane transformations of 5,6-benzo-2-azabarrelenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene
2. Mechanistic organic photochemistry. XXIV. The mechanism of the conversion of barrelene to semibullvalene. A general photochemical process
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4. Control of regioselectivity in the di-.pi.-methane rearrangements. Triplet-sensitized photoisomerization of benzonorbornadienes carrying cyano substituents in the aryl and vinyl segments
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5. ChemInform Abstract: PHOTOCHEMISTRY OF NOVEL AZABICYCLIC COMPOUNDS; CONCERNING THE SITE- AND REGIOSELECTIVITY OF DI-Π-METHANE TRANSFORMATIONS OF 5,6-BENZO-2-AZABARRELENES;Chemischer Informationsdienst;1983-09-27
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