61738-05-4Relevant articles and documents
The Chemistry of Nitrosamines, IV. - Syntheses of α-C-Functionalized N-Nitrosodialkylamines: Esters and Ethers of 1-alcohols
Mueller, Eduard,Kettler, Regina,Wiessler, Manfred
, p. 1468 - 1493 (2007/10/02)
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.
N-Nitrosoenamines, Versatile New Synthesis Intermediates
Kupper, Robert,Michejda, Christopher J.
, p. 2919 - 2921 (2007/10/02)
N-Nitrosoenamines are reactive toward nucleophilic reagents such as dialkylcopper lithium and enolate ions, as well as being active in electrophilic reactions such as acid-catalyzed additions.