Benzotriazole ring cleavage methodology under free radical condition: an ample opportunity in organic synthesis

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dc.contributor.authorYadav M.S.
dc.contributor.authorGupta A.
dc.contributor.authorSingh A.S.
dc.contributor.authorTiwari V.K.
dc.date.accessioned2025-01-13T07:08:37Z
dc.date.available2025-01-13T07:08:37Z
dc.date.issued2024
dc.description.abstractSince long back, benzotriazoles have been used as valuable synthons in organic synthesis. Because of their distinctive structural domain, this favors denitrogenation for easy access to biologically relevant molecules through the benzotriazole ring cleavage (BtRC) methodology followed by the generation of new bonds. Recent developments in transition metal�catalyzed coupling reactions have produced a variety of functionalizations of benzotriazoles as constituents of ortho-amino arene diazonium, primarily including cyclization, arylation, alkenylation, alkylation, carbonylation, and the formation of carbon-heteroatom bonds. In this chapter, we briefly emphasize the growing impact of BtRC methodology exploited under free-radical conditions with their notable features and applications in organic synthesis. � 2024 Elsevier Inc. All rights are reserved including those for text and data mining AI training and similar technologies.
dc.identifier.doi10.1016/B978-0-443-13346-6.00008-7
dc.identifier.isbn978-044313346-6; 978-044313347-3
dc.identifier.urihttps://dl.bhu.ac.in/ir/handle/123456789/3289
dc.language.isoen
dc.publisherElsevier
dc.subjectBenzotriazole ring cleavage
dc.subjectcyclization
dc.subjectfree radical reaction
dc.subjectheterocyclic
dc.titleBenzotriazole ring cleavage methodology under free radical condition: an ample opportunity in organic synthesis
dc.typeBook chapter
journal.titleOrganic Radicals

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