Cu(OTf)2-triggered benzotriazole ring cleavage (BtRC) approach for the synthesis of 2-aryl/alkyl benzoxazoles from N-acylbenzotriazoles

Cu(OTf) is introduced as a novel reagent for the benzotriazole ring cleavage (BtRC) of N-acylbenzotriazoles (RCOBt), followed by cyclization to the corresponding benzoxazoles.This method exhibits unprecedented efficiency, achieving high yields across a broad substrate scope, including aryl and alkyl derivatives, and is scalable from milligram to gram quantities.

Authors

Publication Details

Journal
ARKIVOC
Published
2024-11-19
DOI
https://doi.org/10.24820/ark.5550190.p012.275
Citations
1
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Cu(OTf)2-triggered benzotriazole ring cleavage (BtRC) approach for the synthesis of 2-aryl/alkyl benzoxazoles from N-acylbenzotriazoles

Amrik Singh, Rajesh K. Pandey, Chatrasal Singh Rajput, M. K. Gupta
1 citations
ARKIVOC
Chemical Synthesis and Reactions
0.25
article

Cu(OTf)2-triggered benzotriazole ring cleavage (BtRC) approach for the synthesis of 2-aryl/alkyl benzoxazoles from N-acylbenzotriazoles

Amrik Singh, Rajesh K. Pandey, Chatrasal Singh Rajput, M. K. Gupta
article en
1 citations

Abstract

Cu(OTf) is introduced as a novel reagent for the benzotriazole ring cleavage (BtRC) of N-acylbenzotriazoles (RCOBt), followed by cyclization to the corresponding benzoxazoles.This method exhibits unprecedented efficiency, achieving high yields across a broad substrate scope, including aryl and alkyl derivatives, and is scalable from milligram to gram quantities.

ARKIVOCVol. 2024(1)
Centre International de Recherche sur le Cancer
Zero hunger
Openalex Percentile: Top 46%
Chemical Synthesis and Reactions
0.25
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