Synthesis, characterization and evaluation of antibacterial activity of some thiazolo [3, 2-b][1, 2, 4] triazole incorporating diphenylsulfone moieties
SF Barbuceanu, GL Almajan, I Saramet… - European journal of …, 2009 - Elsevier
A series of thiazolo [3, 2-b][1, 2, 4] triazole incorporating diphenylsulfone moieties were
synthesized starting from 5-[4-(4-X-phenylsulfonyl) phenyl]-4H-1, 2, 4-triazole-3-thioles 3a …
synthesized starting from 5-[4-(4-X-phenylsulfonyl) phenyl]-4H-1, 2, 4-triazole-3-thioles 3a …
The chemistry of sulfur-containing [5, 5]-fused ring systems with a bridgehead nitrogen
F Buron, MA Hiebel, JY Mérour, K Plé… - Advances in Heterocyclic …, 2018 - Elsevier
This review deals with the synthesis and chemical functionalization of sulfur-and nitrogen-
containing [5, 5]-fused ring systems with one nitrogen atom in the bridgehead position and a …
containing [5, 5]-fused ring systems with one nitrogen atom in the bridgehead position and a …
[PDF][PDF] HETEROCYCLES 42. SYNTHESIS AND CHARACTERIZATION OF NEW THIAZOLO [3, 2-B][1, 2, 4] TRIAZOLE DERIVATIVES WITH ANTI-INFLAMMATORY …
Abstract Heterocyclic compounds containing the 1, 2, 4-triazole ring and the thiazolo [3, 2-
b][1, 2, 4] triazole fused ring system in their structure have been reported to exhibit …
b][1, 2, 4] triazole fused ring system in their structure have been reported to exhibit …
First regioselective iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1, 2, 4-triazoles
ND Rode, AD Sonawane, DR Garud, RR Joshi… - Tetrahedron letters, 2015 - Elsevier
The regioselective iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1, 2, 4-triazoles
is described for the first time. The iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1 …
is described for the first time. The iodocyclization reaction of 3-aryl-5-(prop-2-ynylthio)-1H-1 …
[PDF][PDF] Chemistry of 1, 3-thiazin-4-ones and their derivatives, 1995-mid 2018
LJ Silverberg, QJ Moyer - Arkivoc, 2019 - researchgate.net
This review updates an earlier review published in 1996 by Ryabukhin, Korzhavina, and
Suzdalev, which covered the literature through 1994. It deals with the synthesis and …
Suzdalev, which covered the literature through 1994. It deals with the synthesis and …
[PDF][PDF] α, α-Dibromoketones in the convenient synthesis of some triazolo [3, 2-b]-1, 2, 4-triazoles and their antimicrobial activity: Isolation of new intermediates
R Pundeer, SC Sushma, KR Aneja - IJARPB, 2013 - Citeseer
An efficient one pot synthesis of 2, 6-diaryl thiazolo [3, 2-b]-1, 2, 4-triazoles (5) has been
achieved by the reaction of α, α-dibromoacetophenones (1) with 3-aryl-5-mercapto-1, 2, 4 …
achieved by the reaction of α, α-dibromoacetophenones (1) with 3-aryl-5-mercapto-1, 2, 4 …
Direct routes to thiazolotriazoles by cyclization
BF Abdel-Wahab, HA Mohamed - Phosphorus, Sulfur, and Silicon …, 2014 - Taylor & Francis
Methods for the preparation of various fused thiazolotriazoles were reviewed here for the
first time. The main two isomers of fused thiazolotriazoles are thiazolo [3, 2-b][1, 2, 4] triazole …
first time. The main two isomers of fused thiazolotriazoles are thiazolo [3, 2-b][1, 2, 4] triazole …
[HTML][HTML] 二氢乳清酸脱氢酶抑制剂的设计, 合成和构效关系研究
宫荥恢, 刘莉, 齐甜甜, 李洪林, 朱丽丽, 赵振江 - 药学学报, 2017 - html.rhhz.net
本文将实验室前期发现的1-丁酰基-3-(4-氯苯基)-5-甲硫基-1H-1, 2, 4-三氮唑作为人类二氢乳清
酸脱氢酶(HsDHODH) 抑制剂设计的苗头化合物, 为开展结构优化, 首先培养并解析了苗头 …
酸脱氢酶(HsDHODH) 抑制剂设计的苗头化合物, 为开展结构优化, 首先培养并解析了苗头 …