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 CPBA or oxone. This reaction features operational simplicity, divergent synthesis, broad substrate scope, and valuable products.
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http://dx.doi.org/10.1021/acs.orglett.3c01190 | DOI Listing |
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