Issue 15, 2022

K2S2O8-promoted rearrangement of nitrones for the synthesis of benzo[d]oxazoles

Abstract

An efficient route for the synthesis of valuable benzoxazoles has been developed through self-oxidative cyclization with N–O bond cleavage. Readily available nitrones were used as the starting material under simple metal-free reaction conditions. Various functional groups are compatible with this green protocol which can be carried out in one pot easily.

Graphical abstract: K2S2O8-promoted rearrangement of nitrones for the synthesis of benzo[d]oxazoles

Supplementary files

Article information

Article type
Research Article
Submitted
30 Apr 2022
Accepted
15 Jun 2022
First published
15 Jun 2022

Org. Chem. Front., 2022,9, 4034-4040

K2S2O8-promoted rearrangement of nitrones for the synthesis of benzo[d]oxazoles

X. Yang, X. Guo, X. Yuan and B. Chen, Org. Chem. Front., 2022, 9, 4034 DOI: 10.1039/D2QO00680D

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