78224-80-3Relevant academic research and scientific papers
Studies of Heterocyclic Chemistry. Part 25. Intramolecular Cyclizations of N-Acylarylethanethioamides leading to Thiazoles, 4H-1,3-Thiazines, 4H-Pyrido-1,3-thiazines, and 4H-1,3-Benzothiazines
Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Sasaoka, Yoshiro,Kochi, Hirafumi,et al.
, p. 1239 - 1244 (2007/10/02)
Thiazoles, 4H-1,3-thiazines, 4H-pyrido-1,3-thiazines, and 4H-1,3-benzothiazines have been synthesized from N-acyl-(1,3-dithiol-2-ylidene)arylethanethioamides derived from the reactions of 4-aryl-3-halogenoacylthio-4-aryl-3-(2-halogenonicotinoylthio
RING TRANSFORMATIONS OF 4-ARYL-3-HALOACYLTHIO-3-ISOTHIAZOLINE-5-THIONES AS A NEW ACCESS TO THE 4(5H)-THIAZOLONE AND 5,6-DIHYDRO-4H-1,3-THIAZIN-4-ONE RINGS
Nishiwaki, Tarozaemon,Kawamura, Etsuko,Abe, Noritaka,Kochi, Hirafumi,Sasaoka, Yoshiro,Soneda, Kazumi
, p. 595 - 598 (2007/10/02)
The reactions of 4-aryl-3-haloacylthio-3-isothiazoline-5-thiones with reactive acetylenes (e.g. dimethyl acetylenedicarboxylate and dibenzoylacetylene) afford 2--4(5H)-thiazolones and 5,6-dihydro-2-1,3-dithiol-2-ylidene
