Structure of the acylation products from 3,6-disubstituted and 3,6,7-trisubstituted 1H-pyrazolo[5,1-c] [1,2,4]triazoles
Main Authors: | Bercean Vasile-Nicolae, Badea Valentin, Venter Monica, Medeleanu Mihai, Csunderlik Carol |
---|---|
Format: | Article |
Language: | English |
Published: |
Arkat USA, Inc.
2005-04-01
|
Series: | ARKIVOC |
Online Access: | https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0006.a11 |
Similar Items
-
Facile bromination of the benzene ring during the cyclisation of the 1H-3-methyl-4-ethoxycarbonyl-5-arylidenehydrazonopyrazoles to the 3-substituted-aryl-1H-6-methyl-7-ethoxycarbonyl--pyrazolo[3,2-c]-s-triazoles
by: Carol Csunderlik, et al.
Published: (2002-07-01) -
New 1H-1-alkyl-6-methyl-3-phenyl-7-phenylazo-pyrazolo[5,1-c][1,2,4]triazoles through regioselective alkylation of 1H-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles
by: Bercean Vasile-Nicolae, et al.
Published: (2012-04-01) -
Enantiomer stability of atropisomeric 1,5-disubstituted 1,2,3-triazoles
by: Fernanda Meloni, et al.
Published: (2022-03-01) -
Synthesis and Antimycobacterial Activity of 2,5-Disubstituted and 1,2,5-Trisubstituted Benzimidazoles
by: Rogelio Jiménez-Juárez, et al.
Published: (2020-06-01) -
Discovery of New 1,4,6-Trisubstituted-1<i>H</i>-pyrazolo[3,4-<i>b</i>]pyridines with Anti-Tumor Efficacy in Mouse Model of Breast Cancer
by: Maria Georgiou, et al.
Published: (2023-02-01)