A mechanistic study of pyrrole formation in the HBF4-catalyzed thermolysis of cyclopropyl ketimines.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Acid-catalyzed thermolysis of dicyclopropyl ketimines. Substituent effects on the course of the rearrangement
2. General methods of alkaloid synthesis
3. Mechanistic and synthetic studies of the cyclopropyliminium ion rearrangement: an efficient route to enammonium salts and related enamines and dienamines
4. A Simple Pyrrole Synthesisvia an Unusually Facile 1,3 Shift inN-Benzyl-N-(2-benzylaminocyclopropyl)-N-benzylideneammonium Ions
5. Synthesis of some substituted pyrrolidines from cyclopropyl carbonyl compounds
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4. Pyrroles from 1,2-Cyclopropanediamines and Aldehydes;European Journal of Organic Chemistry;1998-08
5. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996
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