Synthesis of Thiolanes from (E)-4-Mercapto-2-butenoatesvia, ConsecutiveMichael Additions
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
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1. Convenient ‘one-pot’ synthesis of 3,4-substituted tetrahydrothiophenes through tandem Michael–Henry and Michael–Michael reactions;Tetrahedron Letters;2006-11
2. Meldrum's Acid in Orgnaic Synthesis;HETEROCYCLES;1991
3. Nucleophilic Addition–Electrophilic Coupling with a Carbanion Intermediate;Comprehensive Organic Synthesis;1991
4. Tandem Vicinal Difunctionalization: β-Addition to α,β-Unsaturated Carbonyl Substrates Followed by α-Functionalization;Organic Reactions;1990-04-05
5. Light-Induced Synthesis of Tricyclic Thiolane Derivatives from 2(5H)-thiophenonesvia consecutive radical ring closure;Helvetica Chimica Acta;1988-03-16
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