Title:
An Improved N-Acylation of 1 H-Benzotriazole Using 2,2′-DipyridylÂ-diÂ-sulfide and Triphenylphosphine

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dc.contributor.authorAnoop S. Singh
dc.contributor.authorAnand K. Agrahari
dc.contributor.authorNidhi Mishra
dc.contributor.authorMala Singh
dc.contributor.authorVinod K. Tiwari
dc.date.accessioned2026-02-07T09:10:20Z
dc.date.issued2019
dc.description.abstractA novel path has been developed for the conversion of carboxylic acids into the corresponding N-acylbenzotriazoles by using 2,2′-dipyridyl disulfide/PPh 3 in anhydrous dichloromethane in the presence of 1 H-benzotriazole. Mild reaction conditions, short reaction time, easy in handling, wide substrate scope, availability of reagents involved, and moreover avoiding the use of base makes this protocol quite useful for the laboratory practices for N-acylbenzotriazole synthesis. © Georg Thieme Verlag Stuttgar.
dc.identifier.doi10.1055/s-0037-1610277
dc.identifier.issn397881
dc.identifier.urihttps://doi.org/10.1055/s-0037-1610277
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/34650
dc.publisherGeorg Thieme Verlag
dc.subjectcoupling reaction
dc.subjectN-acylbenzotriazole
dc.subjectPPh <sub>3</sub>
dc.subjectPySSPy
dc.titleAn Improved N-Acylation of 1 H-Benzotriazole Using 2,2′-DipyridylÂ-diÂ-sulfide and Triphenylphosphine
dc.typePublication
dspace.entity.typeArticle

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