Reaction of a Cyclic Phosphonium Ylide with α,β-Unsaturated Thioesters
Author:
Affiliation:
1. Department of Functional Polymer Science, Faculty of Textile Science and Technology, Shinshu University, Tokida Ueda 386-8567, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo990528q
Reference11 articles.
1. Stereoselective synthesis of trans-hydroazulene derivatives by tandem Michael-intramolecular Wittig reactions of a cyclic phosphonium ylide with alkyl or aryl 1-cyclopentenyl ketones
2. Synthesis of Seven-Membered Cyclic Enol Ether Derivatives from the Reaction of a Cyclic Phosphonium Ylide with α,β-Unsaturated Esters
3. Total Synthesis of (+)-Laurencin. Use of Acetal-Vinyl Sulfide Cyclizations for Forming Highly Functionalized Eight-Membered Cyclic Ethers
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1. Synthesis of Phosphonium Ylides;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023
2. Meyer–Schuster-type rearrangement for the synthesis of α-selanyl-α,β-unsaturated thioesters;Chemical Communications;2021
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4. Morita-Baylis-Hillman Alkylation of Unsaturated Thioesters;Synlett;2010-09-30
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