Formation of Three-Membered Rings by SHi Displacement. Reverse of Cyclopropyl Ring Opening1
Author:
Affiliation:
1. Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada T6G 2G2
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo960879u
Reference27 articles.
1. Regioselective Addition of Atomic Hydrogen to Olefins. Reversible 1-Methyl-5-hexenyl Radical Cyclization in the Solution-Phase Hydrogenation
2. Absolute Rate Constants for the Addition of Atomic Hydrogen to Monosubstituted and Trisubstituted Olefins
3. Homolytic displacements at carbon. Part 8. Synthesis of 1-cyano-2-(trichloroethyl)cyclopropanes from allylcobaloximes via but-3-enylcobaloximes and 1-bromo-1-cyanobut-3-enes
4. Intramolecular homolytic displacement of bromine atoms from carbon in the reaction of but-3-enyl bromides with radicals
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2. PEG400-enhanced synthesis of gem-dichloroaziridines and gem-dichlorocyclopropanes via in situ generated dichlorocarbene;RSC Advances;2013
3. ChemInform Abstract: Formation of Three-Membered Rings by SHi Displacement. Reverse of Cyclopropyl Ring Opening.;ChemInform;2010-08-04
4. Dibromodifluoromethane;Encyclopedia of Reagents for Organic Synthesis;2005-10-15
5. Dibromodifluoromethane;Encyclopedia of Reagents for Organic Synthesis;2005-10-15
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