77469-29-5Relevant articles and documents
Fluoroalkanosulfonyl fluorides-mediated cyclodehydration of β-hydroxy sulfonamides and β-hydroxy thioamides to the corresponding aziridines and thiazolines
Yan, Zhaohua,Guan, Chengbo,Yu, Zhangxin,Tian, Weisheng
supporting information, p. 5788 - 5790 (2013/10/01)
An efficient method for the fluoroalkanosulfonyl fluoride-induced cyclodehydration of β-hydroxy sulfonamides and β-hydroxy thioamides to the corresponding aziridines and thiazolines is reported. Mild reaction conditions, operational simplicity, and high y
Research on radioprotective agents: Δ-2 Thiazolines and homologous derivatives
Robbe,Fernandez,Chapat,et al.
, p. 16 - 24 (2007/10/02)
Compounds derived from Δ-2 thiazoline, Δ-2 thiazolinium iodoalkylate and 4,5-dihydro-1,3 thiazine have been prepared and evaluated as potential antiradiation agents in mice. They generally have a low toxicity and significant radioprotective activity.
Thioenamide Photochemistry
Couture, Axel,Dubiez, Regine,Lablache-Combier, Alain
, p. 842 - 843 (2007/10/02)
In contrast with their oxo-analogues, thioenamides undergo photochemical cyclization to yield isoquinolinethione derivatives which are easily converted into isoquinolones and tetrahydroisoquinolines by treatment with benzeneseleninic anhydride and EtO3BF4
