Efficient Approach to Amide Bond Formation with Nitriles and Peroxides: One-Pot Access to Boronated [beta]-Ketoamides

An efficient, mild and practical approach for the synthesis of amides from nitriles and peroxides is reported in the presence of boron trifluoride ethereate. In this protocol, we utilized peroxides as C1 synthons for the amidation reaction. Also, we successfully prepared boron-containing [beta]-keto...

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Veröffentlicht in:Advanced synthesis & catalysis 2017-09, Vol.359 (17), p.3014
Hauptverfasser: Gore, Babasaheb Sopan, Senadi, Gopal Chandru, Garkhedkar, Amol Milind, Wang, Jeh-Jeng
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container_issue 17
container_start_page 3014
container_title Advanced synthesis & catalysis
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creator Gore, Babasaheb Sopan
Senadi, Gopal Chandru
Garkhedkar, Amol Milind
Wang, Jeh-Jeng
description An efficient, mild and practical approach for the synthesis of amides from nitriles and peroxides is reported in the presence of boron trifluoride ethereate. In this protocol, we utilized peroxides as C1 synthons for the amidation reaction. Also, we successfully prepared boron-containing [beta]-ketoamides in a one-pot assembly from [beta]-ketonitriles. A variety of functional groups were tolerated in moderate to good yields. Radical inhibition studies showed that the reaction proceeded via a non-radical pathway.
doi_str_mv 10.1002/adsc.201700532
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subjects Amides
Boron
Functional groups
Nitriles
Peroxides
title Efficient Approach to Amide Bond Formation with Nitriles and Peroxides: One-Pot Access to Boronated [beta]-Ketoamides
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