<?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%">Rajmane, Archana</style></author><author><style face="normal" font="default" size="100%">Narande, Poonam</style></author><author><style face="normal" font="default" size="100%">Patil, Nita</style></author><author><style face="normal" font="default" size="100%">Kumbhar, Arjun</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Harnessing DABCO ionic salts for synthesis of heterocycles via multi-component reactions</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Papers</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">1</style></keyword><keyword><style  face="normal" font="default" size="100%">4-Diazabicyclo[2.2.2]octane</style></keyword><keyword><style  face="normal" font="default" size="100%">Ionic salts</style></keyword><keyword><style  face="normal" font="default" size="100%">Multi-component reactions</style></keyword><keyword><style  face="normal" font="default" size="100%">Recyclability</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</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%">79</style></volume><pages><style face="normal" font="default" size="100%">5625-5660</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 review article discusses the advancements in synthesis and applications of acidic, basic, and neutral 1,4-diazabicyclo[2.2.2]octane (DABCO) ionic salts in multi-component reactions. Compared to imidazolium-based ionic salts, the number of DABCO-based ionic salts is significantly lower. Recently, there has been increasing focus on these salts due to their selective salt formation capabilities. A significant challenge lies in the limited availability of physical data regarding DABCO-based ionic salts; hence, most of them are not ionic liquids. While many of these salts could be reused several times with only a minimal reduction in their catalytic effectiveness, there is a significant limitation in the availability of DABCO-based salts.&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%">Review</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;2.3&lt;/p&gt;
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