Synthesis and 1H-NMR configurational study of δ3-thiazolines from 2-aza-1,3-dienes

Autor: Barluenga José, Joglar Jeśus, Ortiz Fernando López, Santos Fustero, Carlón Raquel Pérez, Peláez Elvira
Rok vydání: 1992
Předmět:
Zdroj: Tetrahedron. 48:9745-9752
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(01)81191-1
Popis: A [4+1] heterocyclization process involving 2-aza-1,3-dienes and elemental sulphur leading to the synthesis of Δ3-thiazolines with excellent yields is described. A 1D TOCSY and 1D NOESY study of these systems was made in order to establish the configurations of the diastereoisomeric mixture.
Databáze: OpenAIRE