Reaction of. beta.-nitroenamines with electrophilic reagents. Synthesis of. beta.-substituted. beta.-nitroenamines and 2-imino-5-nitro-4-thiazolines
T Tokumitsu, T Hayashi
Index: Tokumitsu, Takao; Hayashi, Takayuki Journal of Organic Chemistry, 1985 , vol. 50, # 9 p. 1547 - 1550
Full Text: HTML
Citation Number: 28
Abstract
In the reaction of la-j with thiocyanogen at 0" C for 1.5 h, la and lb produced only the corresponding P-thiocyanated products, 4a and 4b, in 50% and 81% yields, respectively. If gave a mixture of 4f and the 2-aminothiazole derivative, 5f, which is a cyclization product ...
Related Articles:
[Gokou, Celestin Tea; Pradere, Jean-Paul; Quiniou, Herve Journal of Organic Chemistry, 1985 , vol. 50, # 9 p. 1545 - 1547]
[Gokou, Celestin Tea; Pradere, Jean-Paul; Quiniou, Herve Journal of Organic Chemistry, 1985 , vol. 50, # 9 p. 1545 - 1547]
[Pradere, J. P.; Roze, J. C.; Quiniou, H.; Danion-Bougot, R.; Danion, D.; Toupet, L. Canadian Journal of Chemistry, 1986 , vol. 64, p. 597 - 602]
[Gokou, Celestin Tea; Pradere, Jean-Paul; Quiniou, Herve Journal of Organic Chemistry, 1985 , vol. 50, # 9 p. 1545 - 1547]