Synthese von Thiomorpholin und 2-monoalkylierten Thiomorpholinen via 5, 6-Dihydro-1, 4-thiazine
F Asinger, H Offermanns, D Neuray, P Müller
Index: Asinger,F. et al. Monatshefte fuer Chemie, 1970 , vol. 101, p. 1295 - 1308
Full Text: HTML
Citation Number: 10
Abstract
Abstract Propionaldehyde, n-butyraldehyde and n-valeraldehyde react with ethylenimine in the presence of dimethylformamide or anhydrous K 2 CO 3 to mixtures of 2-monoalkylated 5.6-dihydro-4 H-1.4-thiazines (2–4) and 2-monoalkylated thiazolidines (6–8). When acetaldehyde is inserted in this reaction, solely 2-methyl-thiazolidine (5) could be isolated. By condensation of α-chloroaldehydes with the sodium salt of cysteamine 2-alkyl-5.6- ...
Related Articles:
Mechanistic studies on thiazolidine formation in aldehyde/cysteamine model systems
[Huang, Tzou-Chi; Huang, Lee-Zen; Ho, Chi-Tang Journal of Agricultural and Food Chemistry, 1998 , vol. 46, # 1 p. 224 - 227]
[Yasuhara, Akio; Shibamoto, Takayuki Agricultural and Biological Chemistry, 1989 , vol. 53, # 8 p. 2273 - 2274]