In-Plane Vinylic SN2 Substitution and Intramolecular β Elimination of β-Alkylvinyl(chloro)-λ3-iodanes
Author:
Affiliation:
1. Contribution from the School of Engineering Science, Osaka University, Toyonaka, Osaka 560, Japan, and Faculty of Pharmaceutical Sciences, University of Tokushima, Tokushima 770, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja972267c
Reference31 articles.
1. Application of the extended Hueckel molecular orbital method to the properties of vinyl cations. Conformational energies of some 1-cyclopropylvinyl cations and a comparison of SN2 displacements at saturated and vinyl carbon
2. (b) McMurry, J.Fundamentals of Organic Chemistry, 3rd ed.; Brooks/Cole Publishing Co. Pacific Grove, CA, 1994; p 213.
3. Inversion component in the solvolytic displacement reactions of alkyl-substituted vinyl trifluoromethanesulfonates
4. Stereochemistry of solvolysis of simple vinyl trifluoromethanesulfonate (triflates)
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