Nucleophilic Dechlorocarbomethoxylation of (E)-Methyl β-Chloro-α-methyl-β-(3-bromo- 2,4,6-trimethylphenyl)acrylate
Author:
Affiliation:
1. Department of Organic Chemistry, The Hebrew University, Jerusalem 91904, Israel
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9600565
Reference25 articles.
1. Nucleophilic attacks on carbon–carbon double bonds. Part XVI. Some relative reactivities of the leaving groups (kBr/kCl, kOMs/kCl, and kOBs/kOTs) in vinylic substitutions
2. Substitution and elimination reactions in chloroolefins. II. Reactions of methyl .beta.-chlorocinnamates with methoxide and ethoxide ions
3. Substitution and elimination reactions in chloro olefins. 3. Reactions of methyl .beta.-chlorocinnamates with thiophenoxide ion
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2. Unequivocal SRN1 Route of Vinyl Halides with a Multitude of Competing Pathways: Reactivity and Structure of the Vinyl Radical Intermediate;Accounts of Chemical Research;2003-05-13
3. Nucleophilic Substitution of Methyl β-Chloro-(3-bromo-2,4,6-trimethyl)cinnamate;The Journal of Organic Chemistry;1997-08-01
4. Chapter 3. Reaction Mechanisms . Part (ii) Polar reactions;Annual Reports Section "B" (Organic Chemistry);1997
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