Photochemical Synthesis of Octahydro- and 3a,4,5,6,7,7a-Hexahydro-benzo[b]thiophenes from Methyl (E)-4-Mercapto-2,6-heptadienoate and Alkenes or Alkynesvia Consecutive Radical Ring Closure. Preliminary Communication
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference12 articles.
1. Light-Induced Synthesis of Thiolanes and 2,3-Dihydrothiophenes by Addition of(E)-4-Mercapto-2-butenoates to Alkenes or Alkynes
2. Photochemistry of 5,5-Dimethyl-2(5H)-thiophenone
3. Thiophene chemistry—IX
4. Dissertation, University of Hamburg, 1985;
5. unpublished results.
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2. Radical Cyclization Reactions;Organic Reactions;1996-03-12
3. Photochemistry of Thiophen-2(5H)-ones;Helvetica Chimica Acta;1989-02-01
4. Light-Induced Synthesis of Tricyclic Thiolane Derivatives from 2(5H)-thiophenonesvia consecutive radical ring closure;Helvetica Chimica Acta;1988-03-16
5. Multiple radical additions: an expedient entry into complex frameworks;Journal of the Chemical Society, Chemical Communications;1988
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