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Abstract:
α-Boryl carbonyl species and α-boryl amino compounds are valuable and important frameworks in organic synthesis. However, the strategies that could merge the two scaffolds into one compound, named 1,1-carbonyl amino alkyl boron, are elusive and underdeveloped. Herein, we present an efficient method that could address this gap and produce 1,1-carbonyl amino alkyl borons from readily accessible indoles via oxidation by m-CPBA or oxone. This reaction features operational simplicity, divergent synthesis, broad substrate scope, and valuable products. © 2023 American Chemical Society.
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Organic Letters
ISSN: 1523-7060
Year: 2023
Issue: 22
Volume: 25
Page: 4038-4043
4 . 9
JCR@2023
4 . 9 0 0
JCR@2023
ESI HC Threshold:39
JCR Journal Grade:1
CAS Journal Grade:1
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ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 1
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