<?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%">Kurapati, Chidvilas</style></author><author><style face="normal" font="default" size="100%">Muthukrishnan, M.</style></author><author><style face="normal" font="default" size="100%">Singh, V. Om</style></author><author><style face="normal" font="default" size="100%">Gundla, Rambabu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thallium(III) p-tosylate (TTS) mediated oxidative rearrangement of 2-naphthyl and 2-heteroarylchromanones</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">2-(3-pyridyl)chromones</style></keyword><keyword><style  face="normal" font="default" size="100%">2-(4-pyridyl)chromones</style></keyword><keyword><style  face="normal" font="default" size="100%">2-and 3-(2-theinyl)chromones</style></keyword><keyword><style  face="normal" font="default" size="100%">2-and 3-(3-theinyl)chromones</style></keyword><keyword><style  face="normal" font="default" size="100%">2-and 3-(?-naphthyl) chromones</style></keyword><keyword><style  face="normal" font="default" size="100%">Dehydrogenation</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative rearrangements</style></keyword><keyword><style  face="normal" font="default" size="100%">thallium(III) acetate</style></keyword><keyword><style  face="normal" font="default" size="100%">thallium(III) p-tosylate</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%">SEP</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">61</style></volume><pages><style face="normal" font="default" size="100%">923-927</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 practical and effective approach towards the synthesis of 3-hetroaryl-4H-chromen-4-ones by the oxidative rearrangement of the respective 2-hetroaryl chroman-4-ones using thallium(III) p-tosylate is described. The oxidative rearrangement of alpha and beta-naphthyl and thiophene behave like aryl groups. However, pyridyl groups give only the dehydrogenated product.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">9</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;
	Indian&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	0.491&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%">Kurapati, Chidvilas</style></author><author><style face="normal" font="default" size="100%">Muthukrishnan, Murugan</style></author><author><style face="normal" font="default" size="100%">Singh, V. Om</style></author><author><style face="normal" font="default" size="100%">Gundla, Rambabu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thallium(III) p-tosylate-mediated oxidative [1,2] rearrangement of 2-naphthyl and 2-heteroarylchromanones</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Heterocyclic Chemistry</style></secondary-title></titles><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><volume><style face="normal" font="default" size="100%">59</style></volume><pages><style face="normal" font="default" size="100%">172-177</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">A practical and effective approach towards the synthesis of 3-heteroaryl-4H-chromen-4-ones by the oxidative [1,2] rearrangement of the respective 2-heteroaryl chroman-4-ones using thallium(III) p-tosylate is presented. The oxidative rearrangement of alpha- and beta-naphthyl and thiophene substituents behaves like aryl groups; However, pyridyl substituents gave only dehydrogenated products.</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><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%">2.193</style></custom4></record></records></xml>