<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Katkar, Santosh S.</style></author><author><style face="normal" font="default" size="100%">Mohite, Pravinkumar H.</style></author><author><style face="normal" font="default" size="100%">Gadekar, Lakshman S.</style></author><author><style face="normal" font="default" size="100%">Vidhate, Kaluram N.</style></author><author><style face="normal" font="default" size="100%">Lande, Machhindra K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ZnO-beta zeolite: as an effective and eco-friendly heterogeneous catalyst for the synthesis of benzothiazole derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">Chinese Chemical Letters</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Benzothiazole</style></keyword><keyword><style  face="normal" font="default" size="100%">cyclocondensation</style></keyword><keyword><style  face="normal" font="default" size="100%">heterogeneous catalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO-beta zeolite</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">4</style></number><publisher><style face="normal" font="default" size="100%">ELSEVIER SCIENCE INC</style></publisher><pub-location><style face="normal" font="default" size="100%">360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA</style></pub-location><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">421-425</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A cheap and recyclable ZnO-beta zeolite was used as catalyst for the synthesis of benzothiazole derivatives. This method provides several advantages such as environmental friendliness, short reaction times, high yields, simple work-up procedure and catalyst was successfully reused for four cycles without significant loss of activity. (C) 2009 Machhindra K. Lande. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">0.775</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pandiri, H.</style></author><author><style face="normal" font="default" size="100%">Sharma, D.M.</style></author><author><style face="normal" font="default" size="100%">Gonnade, R.G.</style></author><author><style face="normal" font="default" size="100%">Punji, B.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and characterization of six-membered pincer nickelacycles and application in alkylation of benzothiazole</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Chemical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Active catalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">Alkyl halides</style></keyword><keyword><style  face="normal" font="default" size="100%">Alkylation</style></keyword><keyword><style  face="normal" font="default" size="100%">Atoms</style></keyword><keyword><style  face="normal" font="default" size="100%">Benzothiazole</style></keyword><keyword><style  face="normal" font="default" size="100%">Benzothiazoles</style></keyword><keyword><style  face="normal" font="default" size="100%">Catalyst activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chemical activation</style></keyword><keyword><style  face="normal" font="default" size="100%">Crystallography</style></keyword><keyword><style  face="normal" font="default" size="100%">C–H activation</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen atoms</style></keyword><keyword><style  face="normal" font="default" size="100%">Nickelacycles</style></keyword><keyword><style  face="normal" font="default" size="100%">Pincer complex</style></keyword><keyword><style  face="normal" font="default" size="100%">Pincer complexessix-membered nickelacycle</style></keyword><keyword><style  face="normal" font="default" size="100%">six-membered nickelacycle</style></keyword><keyword><style  face="normal" font="default" size="100%">Spectrum analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Synthesis (chemical)</style></keyword><keyword><style  face="normal" font="default" size="100%">Synthesis and characterizations</style></keyword><keyword><style  face="normal" font="default" size="100%">X ray crystallography</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">129</style></volume><pages><style face="normal" font="default" size="100%">1161-1169</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Six-membered pincer nickelacycle complexes have been synthesized and employed for the catalytic C–H bond alkylation of benzothiazole. The pincer nickelacycle, {κP, κC, κP- (2 - iPr 2POCH 2-C 6H 3- 6 -CH 2OP iPr 2)} NiBr , [(iPr4-POCCCOP)NiBr(2)] was synthesized by the reaction of 1,3 - iPr 2POCH 2-C 6H 4-CH 2OP iPr 2[(iPr4-POCCCOP)-H(1)] with (CH3CN)2NiBr2 in the presence of Et 3N via the C(2)–H activation on ligand 1. Treatment of [(iPr4-POCCCOP)NiBr](2) with AgOAc afforded the complex [(iPr 4-POCCCOP) Ni (OAc)] (3) in good yield. Both the complexes 2 and 3 were characterized by 1H , 13C and 31P -NMR spectral analysis. Further, the molecular structures of complexes 2 and 3 were established by X-ray crystallography. The complex 2 was found to be an active catalyst for the C–H bond alkylation of benzothiazole with alkyl halides containing β–hydrogen atoms. Graphical abstract: Synopsis. Six-membered pincer nickelacycles have been synthesized and structurally characterized, which show catalytic activity for the C–H bond alkylation of benzothiazole with alkyl halides containing β–hydrogen atoms.[Figure not available: see fulltext.].&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;1.235&lt;/p&gt;</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maliyappa, M. R.</style></author><author><style face="normal" font="default" size="100%">Keshavayya, J.</style></author><author><style face="normal" font="default" size="100%">Mallikarjuna, N. M.</style></author><author><style face="normal" font="default" size="100%">Krishna, P. Murali</style></author><author><style face="normal" font="default" size="100%">Shivakumara, N.</style></author><author><style face="normal" font="default" size="100%">Sandeep, Telkar</style></author><author><style face="normal" font="default" size="100%">Sailaja, Krishnamurty</style></author><author><style face="normal" font="default" size="100%">Nazrulla, Mohammed Azeezulla</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, characterization, pharmacological and computational studies of 4, 5, 6, 7-tetrahydro-1, 3-benzothiazole incorporated azo dyes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Molecular Structure</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Azo dyes</style></keyword><keyword><style  face="normal" font="default" size="100%">Benzothiazole</style></keyword><keyword><style  face="normal" font="default" size="100%">CT-DNA</style></keyword><keyword><style  face="normal" font="default" size="100%">DFT</style></keyword><keyword><style  face="normal" font="default" size="100%">tuberculosis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">1179</style></volume><pages><style face="normal" font="default" size="100%">630-641</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The present work describes the synthesis of five novel heterocyclic azo dyes (4a-4e) through conventional diazo-coupling reaction of 4, 5, 6, 7-tetrahydro-1, 3-benzothiazole with various coupling compounds at 0-5 degrees C. The chemical structures of the synthesized azo dyes were characterized by both theoretical and experimental techniques. All the synthesized molecules were evaluated for their antioxidant activity by two different techniques such as DPPH and FRAP. The results indicated that all the synthesized compounds proved to be potent antioxidants. The anti-mycobacterial activity of the azo dyes was tested against M. tuberculosis and the compounds 4a and 4e showed higher activity among the tested dyes. The DNA binding studies showed effective intercalation properties between the azo dyes and CT-DNA. Finally, the molecular docking studies indicated a possible interaction of the azo dyes with target receptor RpsA. (C) 2018 Elsevier B.V. All rights reserved.&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">2.011</style></custom4></record></records></xml>