n-Butyllithium-Induced Tandem [3,3]-Sigmatropic Rearrangement and Carbonyl Olefination of Allyl-1,1-dichlorovinyl Ethers
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, California State University, Northridge, 18111 Nordhoff Street, Northridge, California 91330, United States
Funder
National Science Foundation
Organic Syntheses
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02178
Reference38 articles.
1. aFor reviews of the chemistry of ynol ethers and the methods for the synthesis of ynol ethers, see: Brandsma, L.; Bos, H. J.; Arens, J. F. In The Chemistry of Acetylenes; Viehe, H. G., Ed. Marcel Dekker: New York, 1969; pp 751–860.
2. Tandem Bond-Forming Reactions of 1-Alkynyl Ethers
3. New Sesquiterpenoids from Eugenia jambolana Seeds and Their Anti-microbial Activities
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1. Entry into Lithium Ynolates from α,α,α-Tribromomethyl Ketones: Synthesis of Cyclobutenes via the [2 + 2] Cycloaddition with α,β-Unsaturated Carbonyls;Organic Letters;2024-02-29
2. [3,3]-Sigmatropic rearrangements of propargyl alkynyl ethers. Synthesis of complex dienoates and unsaturated lactones;Organic & Biomolecular Chemistry;2023
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