[EN] ALLOSTERIC BINDING COMPOUNDS<br/>[FR] COMPOSÉS DE LIAISON ALLOSTÉRIQUES
申请人:UNIV AARHUS
公开号:WO2010094289A1
公开(公告)日:2010-08-26
The present invention relates to allosteric binding compounds of formula (I), especially for the treatment of CNS disorders, together with pharmaceutical compositions and methods of treatment including these compounds.
The present invention relates to allosteric binding compounds of formula (I), especially for the treatment of CNS disorders, together with pharmaceutical compositions and methods of treatment including these compounds.
On the properties of the anions derived from α-deprotonation of α-(o-carboran-1-yl)- and α-ferrocenyl-1-alkylbenzotriazoles
作者:S. K. Moiseev、M. A. Cherevatskaya、T. A. Verbitskaya、I. V. Glukhov、A. S. Peregudov、V. N. Kalinin
DOI:10.1007/s11172-012-0268-2
日期:2012.10
by reactions of the generated carbanions with MeI give the corresponding α-methylated products. Even at room temperature, they exist in solution as an equilibrium mixture of two conformers due to steric crowding around the Cα atom. In contrast, the anions generated by deprotonation of α-ferrocenyl derivatives of 1-methyl- and 1-ethylbenzotriazoles are ambident and are attacked by electrophiles at both
Studies on the thermal decarboxylation of 1-alkoxycarbonylbenzotriazoles
作者:Alan R. Katritzky、Gui-Fen Zhang、Wei-Qiang Fan、Jing Wu、Juliusz Pernak
DOI:10.1002/poc.610061007
日期:1993.10
1-Alkoxycarbonylbenzotriazoles on thermolysis lose carbon dioxide; the decarboxylation is accompanied by the formation of a mixture of 1- and 2-alkylbenzotriazoles, with the N-1 isomer predominating over the N-2 isomer in all cases. A cross-over experiment, in which heating equimolar amounts of 1-benzyloxycarbonylbenzotriazole and 1-(4-methylbenzyloxycarbonyl)-5,6-dimethylbenzotriazole gave almost
Carbonylative coupling of <i>N</i>-chloroamines with alcohols: synthesis of esterification reagents
作者:Zhiping Yin、Zechao Wang、Xiao-Feng Wu
DOI:10.1039/c8ob00462e
日期:——
the carbonylative synthesis of carbamates. Starting from N-chloroamines and alcohols, with copper or Pd/C as the catalyst, the corresponding carbamates were produced in moderate to good yields. No additional oxidant or base is needed in this system. Notably, the produced benzotriazole-carboxylates can be used as esterification reagents.