The Chemistry of Nitrosamines, IV. - Syntheses of α-C-Functionalized N-Nitrosodialkylamines: Esters and Ethers of 1-alcohols
Imines (Schiff's bases) and nitrosyl chloride react to give N-alkyl-1-chloro-N-nitrosoalkylamines 13.Nucleophilic substitution by acetate or p-nitrobenzoate affords the acetates 7 and 9 and p-nitrobenzoates 8 and 10, respectively.The spectroscopic and chemical data of the newly synthesized compounds are discussed.
Mueller, Eduard,Kettler, Regina,Wiessler, Manfred
p. 1468 - 1493
(2007/10/02)
ISOLATION AND CHARACTERIZATION OF N-ALKYL-N-(HYDROXYMETHYL)NITROSAMINES FROM N-ALKYL-N-(HYDROPEROXYMETHYL)NITROSAMINES BY DEOXYGENATION
N-Alkyl-N-(hydroxymethyl)nitrosamines, postulated intermediates in the metabolic activation of carcinogenic nitrosamines , were prepared by deoxygenation of the corresponding hydroperoxymethyl nitrosamines and characterized
Mochizuki, Masataka,Anjo, Takako,Okada, Masashi
p. 3693 - 3696
(2007/10/02)
Oxidative decarboxylation of nitrosoamino acids: A synthetic approach to cyclic α-acetoxynitrosamines
-
Saavedra
p. 1923 - 1926
(2007/10/05)
More Articles about upstream products of 56856-83-8