New method for increasing of electrophilicity of weak electrophiles in addition reactions
- 1 January 1975
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 31 (23) , 2948-2952
- https://doi.org/10.1016/0040-4020(75)80317-6
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Hydrolysis of Alkyl Halides Induced by Metal Ions: M+–SN1 and M+–SN2 ReactionsRussian Chemical Reviews, 1974
- The Isolation of an Episelenurane from the Reaction of 4-Tolueneselenenyl Chloride with EthyleneCanadian Journal of Chemistry, 1974
- Electrophilic additions to strained olefinsAccounts of Chemical Research, 1969
- Nitrosochlorination of AlkenesRussian Chemical Reviews, 1968
- Molecular geometry of the norbornyl cation. I. Synthesis and acetolysis of the exo- and endo-4,5-exo-trimethylene-2-norbornyl p-toluenesulfonatesJournal of the American Chemical Society, 1967
- Electrophilic Addition to Olefins. II.1 Addition of Deuterium Halides to Indene; the Mechanism of Addition2Journal of the American Chemical Society, 1963
- Electrophilic Addition to Olefins. I. The Stereochemistry of Addition of Deuterium Halides to AcenaphthyleneJournal of the American Chemical Society, 1963
- Salt Effects and Ion Pairs in Solvolysis and Related Reactions. XXI.1 Acetolysis, Bromide Exchange and the Special Salt Effect2Journal of the American Chemical Society, 1961
- Neighboring Carbon and Hydrogen. XI. Solvolysis of exo-Norbornyl p-Bromobenzenesulfonate1,2,3Journal of the American Chemical Society, 1952
- Neighboring Carbon and Hydrogen. X. Solvolysis of endo-Norbornyl Arylsulfonates1,2,3Journal of the American Chemical Society, 1952