180793-11-7Relevant articles and documents
Structure of cyanoacetylhydrazones of aldehydes and ketones
Zelenin,Oleinik,Alekseev,Potekhin
, p. 1116 - 1120 (2001)
1D 1H and 13C, and 2D 1H NOESY NMR were used to establish that cyanoacetylhydrazones of aliphatic and aromatic aldehydes and ketones in CDCl3 and (CD3)2SO solutions have a linear structure,
1H, 13C and 15N NMR of spiro acridines integrated with pyrrole scaffolds
Vilková, Mária,?oral, Michal,Be?ka, Michal,Poto?ňák, Ivan,Sabolová, Danica,Béres, Tibor,Du?ek, Michal,Imrich, Ján
, p. 204 - 214 (2019/12/24)
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N-Substituted cyanacetohydrazides in the synthesis of 3,3-dialkyl-1,2,3,4-tetrahydroisoquinolines by Ritter reaction
Mikhailovskii, Alexander G.,Korchagin, Denis V.,Yusov, Aleksey S.,Gashkova, Oksana V.
, p. 1114 - 1119 (2017/12/08)
[Figure not available: see fulltext.] Cyanacetohydrazide, protected at the nitrogen atom of hydrazide group, underwent cyclocondensation by Ritter reaction with 3,3-dialkylbenzylcarbinols, forming 3,3-dialkyl-1,2,3,4-tetrahydroisoquinolines. The reagents
Microwave assisted synthesis and evaluation of N-cinnamoyl aryl hydrazones for cytotoxic and antioxidant activities
Devi, T. Sarala,Rajitha
, p. 1703 - 1709 (2016/08/06)
A series of N-cinnamoyl aryl hydrazones 2a-2i were synthesized in good yields by microwave irradiation technique. The title compounds were formed by nucleophilic condensation of various N1- substituted benzylidene-2-cyano aceto hydrazides with