Diastereofacial selectivity in Diels-Alder cycloadditions involving vinyl sulfoxides
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (50) , 6041-6044
- https://doi.org/10.1016/s0040-4039(00)85393-9
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Asymmetric additions of 1-alkenylcopper reagents to chiral enoates: Enantioselective synthesis of california red scale pheromone.Tetrahedron Letters, 1986
- Self-induced diastereoselective oxidation of vinyl sulfoxides bearing a chiral hydroxy group as a way of preparation of optically active sulfinyl dienophiles and their use in the asymmetric Diels-Alder reactions to cyclopentadieneThe Journal of Organic Chemistry, 1986
- Six-membered ring-fused thiirene S-oxides. Synthesis, characterization, and reactivityThe Journal of Organic Chemistry, 1986
- Un dienophile chiral tres reactif : le Z-(R)S p-tolylsulfinyl-3 propenoate de methyleTetrahedron Letters, 1984
- Highly diastereoselective Diels-Alder reaction of optically active ethyl 2-p-tolylsulfinylmethylenepropionate with cyclopentadieneTetrahedron Letters, 1984
- Camphor‐Derived N‐Acryloyl and N‐Crotonoyl Sultams: Practical Activated Dienophiles in Asymmetric Diels‐alder Reactions. Preliminary CommunicationHelvetica Chimica Acta, 1984
- Diels-Alder reactions of S-vinyl-S-arylsulfoximinesThe Journal of Organic Chemistry, 1984
- Chirality Transfer via Sigmatropic RearrangementsPublished by Elsevier ,1984
- Investigation of a chiral masked ketene synthon synthesis of the (+)-(1r4r) and (−)-1s,4s) enantiomers of dehydronorcamphorTetrahedron, 1983
- High asymmetric induction in the 1,3-dipolar cycloaddition of (R)-(+)-p-tolyl vinyl sulfoxide with acyclic nitronesThe Journal of Organic Chemistry, 1982