Simple and stereoselective synthetic route to (E)-1-alkenyl sulfoxides via terminal alkynes
Author:
Affiliation:
1. Permanent address: Department of Chemistry, Yichun Normal Institute, Yichun, 336000, P.R. China
2. Department of Chemistry, Zhejiang University, Xixi Campus, Hangzhou, 310028, P.R. China
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823400103166300
Reference14 articles.
1. The role of sulfur functionalities in activating and directing olefins in cycloaddition reactions
2. Asymmetric synthesis using α,β-unsaturated sulfoxides. Creation of both (R)- and (S)-asymmetric centers from a single chiral origin.
3. Additive Pummerer rearrangements. Asymmetric synthesis of (–)-methyl jasmonate
4. Horner-Wittig Reactions in a Two-Phase System in the Absence of a Typical Phase-Transfer Catalyst1
5. Reactions of 2-halovinyl aryl sulfoxides with organometallic reagents
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1. Hydrozirconation of Alkynes;Organic Reactions;2023-08-09
2. Efficient synthesis of racemic and chiral alkenyl sulfoxides by palladium-catalyzed Suzuki coupling;Tetrahedron;2010-08
3. ChemInform Abstract: Simple and Stereoselective Synthetic Route to (E)-1-Alkenyl Sulfoxides via Terminal Alkynes.;ChemInform;2001-05-15
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