87857-70-3Relevant academic research and scientific papers
A convenient method for the conversion of a carboxy group into a 4,6-dimethoxy-1,3,5-triazine group: Application to N-benzylpyroglutamic acids
Oudir, Souhila,Rigo, Benoit,Henichart, Jean-Pierre,Gautret, Philippe
, p. 2845 - 2848 (2006)
Reaction of an activated form of carboxylic acids with a stoichiometric amount of zinc dimethyl imidodicarbonimidate (in CH2Cl 2-pyridine with molecular sieves), led to 4,6-dimethoxy-1,3,5- triazines in high yields. This method has b
Studies on pyrrolidinones: Chemistry of dimethoxytriazines
Lucescu, Liliana,Gautret, Philippe,Oudir, Souhila,Rigo, Benoit,Belei, Dalila,Bicu, Elena,Ghinet, Alina
, p. 1333 - 1340 (2013/07/04)
The synthesis of dimethoxytriazine-containing N-aryl substituted pyrrolidinones is realized for the first time. Three new modes of reactivity for these substrates possessing a 4,6-dimethoxy-1,3,5-triazine unit are discussed. Their treatment with acid lead
Studies on Pyrrolidinones. Derivatives of 1,2,3,5,10,10a-Hexahydrobenzindolizine-3,10-dione
Rigo, Benoit,Kolocouris, Nicolas
, p. 893 - 898 (2007/10/02)
The Friedel-Crafts reaction of N-(arylmethyl)-5-pyrrolidinone-2-carboxylic acids gives either a cyclization or a reaction with benzene (used as a solvent).Reactions such as reduction, keto substitution and lactam ring opening of 1,2,3,5,10,10a-hexahydrobe
