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DOI: 10.1055/a-1558-7457
A Domino Approach for the Synthesis of 4-Carboxamide Oxazolines from Azirines
We thank the Iran National Science Foundation (INSF, Grant No. 97005171) for financial support.
Abstract
A regio- and diastereoselective ring-expansion reaction of N-acylaziridines is described for the synthesis of 4-carboxamide oxazolines using InCl3. A domino Ugi–Joullié/ring-expansion reaction of arylphenylazirines, isocyanides, and carboxylic acids leads to the target products through the N-acylaziridine intermediates in the presence of the indium catalyst. The oxazolines were synthesized in moderate to excellent yields with high atom economy and high bond-forming efficiency under mild reaction conditions.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-1558-7457.
- Supporting Information
Publication History
Received: 17 December 2020
Accepted after revision: 26 July 2021
Accepted Manuscript online:
26 July 2021
Article published online:
17 August 2021
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For selected reviews on ring-expansion reactions, see:
For recent selected reports, see:
For selected reviews on ring-expansion reactions of aziridines and 2H-azirines, see:
Synthesis of pyrazines:
Pyridines:
For recent selected reports on the synthesis of pyrroles, see:
Oxazoles: