Iodine(III)-Mediated Contraction of 3,4-Dihydropyranones: Access to Polysubstituted γ-Butyrolactones
Author:
Affiliation:
1. Centre in Green Chemistry and Catalysis, Department of Chemistry, University of Sherbrooke, 2500 boul. de l’Université, Sherbrooke, Québec J1K 2R1, Canada
Funder
Canada Foundation for Innovation
Fonds de Recherche du Qu?bec - Nature et Technologies
Universit? de Sherbrooke
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b01893
Reference42 articles.
1. Synthetic approaches towards structurally diverse γ-butyrolactone natural-product-like compounds
2. A continuing challenge: N-heterocyclic carbene-catalyzed syntheses of γ-butyrolactones
3. Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones
4. Studies toward the syntheses of functionally substituted .gamma.-butyrolactones and spiro-.gamma.-butyrolactones and their reaction with strong acids: a novel route to .alpha.-pyrones
5. A highly versatile synthesis of 2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropane-1-carboxylic acid esters
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