118498-98-9Relevant articles and documents
The use of mixtures of ligands in the Ir-catalyzed asymmetric reductive amination of 6-methyl-2,3,4,9-tetrahydro-1H-carbazol-1-one
Lyubimov,Ozolin,Pavlov,Ivanov, P. Yu,Mayorov,Velezheva,Davankov,Nikonenko
, p. 1591 - 1594 (2015)
A comparative testing of complex catalysts with homo and hetero combinations of chiral and achiral monodentate phosphite- and phosphine-type ligands in the Ir-catalyzed asymmet- ric direct reductive amination of 2,3,4,9-tetrahydro-1H-carbozol-1-ones was carried out. A positive effect of the use in the reaction of a mixture of chiral and achiral ligands was demonstrated. This approach makes feasible a one-pot synthesis of valuable biologically active compounds of (tetrahydro-1H-carbazol-1-yl)amine series.
COMPOSITIONS AND METHODS FOR VIRAL INHIBITION
-
Page/Page column 37, (2010/02/11)
The present invention discloses methods and compositions for viral inhibition, particularly inhibition of HCV and SARS. The invention also provides compositions including carbazole derivatives useful for viral inhibition.
SYNTHESIS OF HETEROCYCLES ON THE BASIS OF IMINOTETRAHYDROCARBAZOLES. 1. 3-BENZYL-8-METHYL-2-OXO-2,3,3a,4,5,6-HEXAHYDRO-1H-PYRAZINOCARBAZOLE
Bokanov, A. I.,Ivanov, P. Yu.,Akalaeva, T. V.,Bogdanova, G. A.,Shvedov, V. I.
, p. 1311 - 1315 (2007/10/02)
The reaction of 6-methyl-1-oxo-1,2,3,4-tetrahydrocarbazole and benzylamine gave 1-benzylimino-6-methyl-1,2,3,4-tetrahydrocarbazole, which was converted by two methods to a pyrazinocarbazole derivative.The promising character of the use of iminotetrahydroc
