<?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%">Pansare, Vaibhav Ramchandra</style></author><author><style face="normal" font="default" size="100%">Sreelakshmi, N.</style></author><author><style face="normal" font="default" size="100%">Barsu, Nagaraju</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Site-selective iron-catalyzed C-H alkylation of pyrazinones, azauracils and quinoxalinones</style></title><secondary-title><style face="normal" font="default" size="100%">Organic Chemistry Frontiers</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY </style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">2725-2729</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Described herein is an unprecedented iron-catalyzed C(sp2)-H alkylation of pyrazinone, azauracil, and quinoxalinone analogues using ethers and benzyl derivatives, offering broad scope and high functional group tolerance. The method is scalable and enables downstream functionalization. The mechanistic investigations, such as radical trapping, support a radical-mediated pathway.&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;
	Foreign&lt;/p&gt;
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	4.7&lt;/p&gt;
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