1. Bildung tricyclischer Thietan-Derivate durch intramolekulare (2+2)-Cycloaddition
- Author
-
Peter Wipf, Heinz Heimgartner, University of Zurich, and Heimgartner, Heinz
- Subjects
Thietane ,10120 Department of Chemistry ,1303 Biochemistry ,Intramolecular reaction ,1503 Catalysis ,1604 Inorganic Chemistry ,3002 Drug Discovery ,Organic Chemistry ,Free-radical reaction ,Photochemistry ,Biochemistry ,Medicinal chemistry ,Catalysis ,Cycloaddition ,Inorganic Chemistry ,chemistry.chemical_compound ,chemistry ,Intramolecular force ,Drug Discovery ,540 Chemistry ,Physical and Theoretical Chemistry ,1606 Physical and Theoretical Chemistry ,Dichloromethane ,1605 Organic Chemistry - Abstract
Formation of Thietane Derivatives via Intramolecular (2+2) Cycloaddition On irradiation, the two 4-vinyl-1,3-thiazole-5(4H)-thiones 1a, b, synthesized from thiobenzoic acid and the corresponding 3-amino-2H-azirines 2a,b, undergo an intramolecular (2+2)-cycloaddition reaction of the CS and CC bonds to give the tricyclic thietane derivatives 3a,b.
- Published
- 1987