56475-82-2Relevant articles and documents
Self-immolative base-mediated conjugate release from triazolylmethylcarbamates
Blencowe, Christopher A.,Thornthwaite, David W.,Hayes, Wayne,Russell, Andrew T.
, p. 8703 - 8707 (2015)
A range of carbamate functionalized 1,4-disubstituted triazoles featuring a base sensitive trigger residue, plus a model aromatic amine reporter group, were prepared via copper(i) catalysed azide-alkyne cycloaddition and evaluated for their self-immolativ
Methoxycarbonylation of Alkyl-, Cycloalkyl-, and Arylamines with Dimethyl Carbonate in the Presence of Binder-Free Zeolite
Khazipova, A. N.,Khusnutdinov, R. I.,Mayakova, Yu. Yu.,Shchadneva, N. A.
, p. 1228 - 1235 (2020/10/02)
Abstract: Methyl N-alkyl-, N-cycloalkyl-, and N-arylcarbamates were synthesized by reaction of the correspondingamines with dimethyl carbonate in the presence of binder-free FeHY zeolite. Theoptimal conditions (reactant ratio, amount of the catalyst, temperature,reaction time) were found to afford the target products with high yields.
Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization
Adachi, Satoshi,Onozuka, Masao,Yoshida, Yuko,Ide, Mitsuaki,Saikawa, Yoko,Nakata, Masaya
supporting information, p. 358 - 361 (2014/04/03)
Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.
