Nucleophilic Vinylic Substitution (SNV) of Trisubstituted Monofluoroalkenes for the Synthesis of Stereodefined Trisubstituted Alkenes and Divinyl Ethers-Reference-Cited by-同舟云学术

Nucleophilic Vinylic Substitution (SNV) of Trisubstituted Monofluoroalkenes for the Synthesis of Stereodefined Trisubstituted Alkenes and Divinyl Ethers

Published:2021-07-27 Issue:15 Volume:23 Page:6169-6173
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zong Yuwei,Ma Qiao,Tsui Gavin Chit¹^ORCID

Affiliation:

1. Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China

Funder

Research Grants Council, University Grants Committee

Chinese University of Hong Kong

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02359

Reference36 articles.

1. Recent Advances in Our Mechanistic Understanding of SNV Reactions

2. Concerted Nucleophilic Substitution Reactions at Vinylic Carbons

3. Nucleophilic vinylic substitution. A single- or a multi-step process?

4. Unraveling Structure−Reactivity Relationships in SNV Reactions: Kinetics of the Reactions of Methoxybenzylidenemalononitrile, 2-(Methylthiobenzylidene)-1,3-indandione, 2-(Benzylthiobenzylidene)-1,3-indandione, and Methyl β-Methylthio-α-nitrocinnamate with OH- and Thiolate Ions in Aqueous DMSO

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