A new family of potential oncostatics: 2-chloroethylnitrososulfamides (CENS)—I. Synthesis, structure, and pharmacological evaluation (preliminary results)
M Abdaoui, G Dewynter, N Aouf, G Favre…
Index: Abdaoui, Mohamed; Dewynter, Georges; Aouf, Nourredine; Favre, Gilles; Morere, Alain; Montero, Jean-Louis Bioorganic and Medicinal Chemistry, 1996 , vol. 4, # 8 p. 1227 - 1235
Full Text: HTML
Citation Number: 34
Abstract
A new series of alkylating agents, 2-chloroethylnitrososulfamides (CENS), were developed on the model of 2-chloroethylnitrosoureas. Starting from chlorosulfonyl isocyanate, a four- step synthesis (carbamoylation-sulfamoylation, Mitsunobu alkylation, deprotection, and nitrosation) gives the title compounds in a 47–58% overall yield. The selection of the nitrosation site can be directed through an alternative route. The pharmacological ...
Related Articles:
[Winum; Toupet; Barragan; Dewynter; Montero Organic letters, 2001 , vol. 3, # 14 p. 2241 - 2243]