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 Alkynes via Consecutive Radical Ring Closure. Preliminary Communication
- 4 February 1987
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 70 (1) , 121-124
- https://doi.org/10.1002/hlca.19870700114
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Photochemistry of 5,5-Dimethyl-2(5H)-thiophenoneHelvetica Chimica Acta, 1985
- Regio- and stereo-selectivity of alkenyl radical ring closure: A theoretical studyTetrahedron, 1985
- Light-Induced Synthesis of Thiolanes and 2,3-Dihydrothiophenes by Addition of(E)-4-Mercapto-2-butenoates to Alkenes or AlkynesHelvetica Chimica Acta, 1984
- Regio-selectivity and stereo-selectivity in radical reactionsTetrahedron, 1981
- Some guidelines for radical reactionsJournal of the Chemical Society, Chemical Communications, 1980
- Synthese de systemes thia-6 bicyclo(3.2.1)octaniques par photolyse de methylthio-1 cyclohexene-3Tetrahedron, 1976
- Rules for ring closureJournal of the Chemical Society, Chemical Communications, 1976
- Conformational analysis. CVIII. Calculation of the structures and energies of alkanethiols and thiaalkanes by the molecular mechanics methodJournal of the American Chemical Society, 1975
- Thiophene chemistry—IXTetrahedron, 1963