<?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%">Kulkarni, Anand M.</style></author><author><style face="normal" font="default" size="100%">Mullapudi, Venkannababu</style></author><author><style face="normal" font="default" size="100%">Ramana, Chepuri Venkata</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Iridium-catalyzed synthesis of pyrazolone fused 1,4-dihydrocinnolin-3-one employing alpha-diazotized Meldrum's acid</style></title><secondary-title><style face="normal" font="default" size="100%">ARKIVOC</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">?-diazotized Meldrum's acid</style></keyword><keyword><style  face="normal" font="default" size="100%">C-H activation</style></keyword><keyword><style  face="normal" font="default" size="100%">carbene Insertion</style></keyword><keyword><style  face="normal" font="default" size="100%">cinnoline derivatives</style></keyword><keyword><style  face="normal" font="default" size="100%">N-arylpyrazolones</style></keyword><keyword><style  face="normal" font="default" size="100%">[Iri-Catalysis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JAN</style></date></pub-dates></dates><pages><style face="normal" font="default" size="100%">179-190</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 [Iri-catalysed carbenoid insertion and cyclization of N-arylpyrazolones has been carried out with alpha-diazotized Meldrum's acid to access tricyclic pyrazolone fused 1,4-dihydrocinnolin-3-one derivatives. Further, the selective reduction of these tricyclic derivatives has been studied under Birch reduction conditions.&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%">&lt;p&gt;Foregn&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	0.689&lt;/p&gt;
</style></custom4></record></records></xml>