Efficient one-pot synthesis of 1-chlorovinyl p -tolyl sulfoxides from aldehydes and ketones by the Horner-Wadsworth-Emmons reaction
Author:
Affiliation:
1. Department of Chemistry; Graduate School of Science; Tokyo University of Science; Tokyo Japan
Publisher
Wiley
Subject
General Chemistry
Reference42 articles.
1. Development of new synthetic methods with aryl 1-chlorovinyl sulfoxides
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3. Direct alkenylation of arylamines at the ortho-position with magnesium alkylidene carbenoids and some theoretical studies of the reactions
4. Direct N- and C-alkenylation of nitrogen-containing heterocycles with magnesium alkylidene carbenoids
5. Alkenylation of thiophenes and furans at the 2-position and a synthesis of allenes conjugated with α,β-unsaturated ester with magnesium alkylidene carbenoids
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1. DFT and experimental characterization of 1-heteroatom-substituted alkylmagnesium chlorides;Journal of Organometallic Chemistry;2024-10
2. Use of 1-chlorovinyl p-tolyl sulfoxides as alkynylmagnesium chloride sources;Tetrahedron;2023-06
3. Magnesium Carbenoids in Homologation Chemistry;Homologation Reactions;2023-05-26
4. Fritsch–Buttenberg–Wiechell rearrangement of magnesium alkylidene carbenoids leading to the formation of alkynes;Beilstein Journal of Organic Chemistry;2021-05-28
5. Application of liposome membrane as the reaction field: A case study using the Horner–Wadsworth–Emmons reaction;Journal of Bioscience and Bioengineering;2019-08
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