946529-80-2Relevant articles and documents
A novel isocyanide-based three-component reaction: Synthesis of highly substituted 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives
Shaabani, Ahmad,Maleki, Ali,Moghimi-Rad, Jafar
, p. 6309 - 6311 (2007)
(Chemical Equation Presented) A novel multi-component synthesis of highly substituted 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives starting from simple and readily available inputs is described. Thus, simply stirring an ethanol solution of 2,3-diami
Revisiting the reaction between diaminomaleonitrile and aromatic aldehydes: A green chemistry approach
Rivera, Augusto,Rios-Motta, Jaime,Leon, Francisco
, p. 858 - 866 (2007/10/03)
The reaction between diaminomaleonitrile (DAMN) and aldehydes and the resulting monoimines are well known. Since the standard reaction conditions involve the use of toxic solvents (typically methanol), we have sought to apply green chemistry principles to
Synthesis of porphyrazine-octaamine, hexamine and diamine derivatives
Fuchter, Matthew J.,Beall, L. Scott,Baum, Sven M.,Montalban, Antonio Garrido,Sakellariou, Efstathia G.,Mani, Neelakandha S.,Miller, Todd,Vesper, Benjamin J.,White, Andrew J. P.,Williams, David J.,Barrett, Anthony G. M.,Hoffman, Brian M.
, p. 6115 - 6130 (2007/10/03)
The syntheses of a variety of substituted diaminomaleonitriles, with variable nitrogen substituents, were undertaken. Linstead macrocyclization of the resulting diaminomaleonitriles gave access to a wide range of functionalized porphyrazine-octaamines and
