Diminished Reactivity of Ortho-Substituted Phenacyl Bromides toward Nucleophilic Displacement
Author:
Affiliation:
1. Chemical Development Department, GlaxoSmithKline Co., 5 Moore Drive, Research Triangle Park, North Carolina 27709 barry.r.sickles@gsk.com
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo011042o
Reference11 articles.
1. Stereochemical and Steric Effects in Nucleophilic Substitution of α-Halo Ketones
2. The Effect of the Carbonyl and Related Groups on the Reactivity of Halides in SN2 Reactions
3. Synthesis and evaluation of the anticonvulsant activity of a series of 2-amino-1-phenyl-1-propanols derived from the metabolites of the antidepressant bupropion
4. Dewar, M. J. S.The Electronic Theory of Organic Chemistry; Oxford University Press: London, England, 1949; p 73. And later: Carey, F. A.; Sundberg, R. J.Advanced Organic Chemistry, 3rd ed.; Plenum Press: New York, 1990; Part A, p 296.
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