114081-67-3Relevant articles and documents
New synthesis of 3-(β-D-glucopyranosyl)-5-substituted-1,2,4-triazoles, nanomolar inhibitors of glycogen phosphorylase
Kun, Sándor,Bokor, éva,Varga, Gergely,Szocs, Béla,Páhi, András,Czifrák, Katalin,Tóth, Marietta,Juhász, László,Docsa, Tibor,Gergely, Pál,Somsák, László
, p. 567 - 579 (2014/04/03)
O-Perbenzoylated 5-(β-D-glucopyranosyl)tetrazole was reacted with N-benzyl carboximidoyl chlorides to give the corresponding 4-benzyl-3-(β-D- glucopyranosyl)-5-substituted-1,2,4-triazoles. Removal of the O-benzoyl and N-benzyl protecting groups by base catalysed transesterification and catalytic hydrogenation, respectively, furnished a series of 3-(β-D-glucopyranosyl)- 5-substituted-1,2,4-triazoles with aliphatic, mono- and bicyclic aromatic, and heterocyclic substituents in the 5-position. Enzyme kinetic studies revealed these compounds to inhibit rabbit muscle glycogen phosphorylase b: best inhibitors were the 5-(4-aminophenyl)- (Ki 0.67 μM) and the 5-(2-naphthyl)-substituted (Ki 0.41 μM) derivatives. This study uncovered the C-glucopyranosyl-1,2,4-triazoles as a novel skeleton for nanomolar inhibition of glycogen phosphorylase.
Parallel copper catalysis: Diastereoselective synthesis of polyfunctionalized azetidin-2-imines
Xing, Yanpeng,Zhao, Hongyang,Shang, Qiongyi,Wang, Jing,Lu, Ping,Wang, Yanguang
supporting information, p. 2668 - 2671 (2013/07/19)
An efficient and diastereoselective synthesis of highly functionalized azetidin-2-imines has been achieved through a parallel catalysis strategy, including a copper-catalyzed azide-alkyne cycloaddition, a copper-catalyzed Csp-Csp2 cr
PROTOTROPIC MIGRATIONS IN THE PHOSPHORYLATION OF IMIDOYL CHLORIDES CONTAINING HYDROGEN ON THE N-α-CARBON ATOM. III. PHOSPHORYLATION OF SUBSTITUTED N-BENZYLBENZIMIDOYL CHLORIDES WITH TRIETHYL PHOSPHITE
Onys'ko, P. P.,Kim, T. V.,Kiseleva, E. I.,Sinitsa, A. D.
, p. 1104 - 1110 (2007/10/02)
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