An organocatalytic C-C bond cleavage approach: a metal-free and peroxide-free facile method for the synthesis of amide derivatives

A facile organocatalytic approach has been devised towards the synthesis of amide derivatives using 1,3-dicarbonyls as easily available acyl-sources under peroxide-free reaction conditions. This transformation was accomplished by the cleavage of the C-C bond in the presence of TEMPO as an organocata...

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Veröffentlicht in:New journal of chemistry 2020-12, Vol.44 (48), p.294-2944
Hauptverfasser: Vodnala, Nagaraju, Gujjarappa, Raghuram, Polina, Saibabu, Satheesh, Vanaparthi, Kaldhi, Dhananjaya, Kabi, Arup K, Malakar, Chandi C
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container_end_page 2944
container_issue 48
container_start_page 294
container_title New journal of chemistry
container_volume 44
creator Vodnala, Nagaraju
Gujjarappa, Raghuram
Polina, Saibabu
Satheesh, Vanaparthi
Kaldhi, Dhananjaya
Kabi, Arup K
Malakar, Chandi C
description A facile organocatalytic approach has been devised towards the synthesis of amide derivatives using 1,3-dicarbonyls as easily available acyl-sources under peroxide-free reaction conditions. This transformation was accomplished by the cleavage of the C-C bond in the presence of TEMPO as an organocatalyst and excludes the use of transition-metals and harsh reaction conditions. A broad range of substrates with diverse functional groups were well tolerated and delivered the products in high yields. An organocatalyzed C-C bond cleavage approach has been envisioned towards the synthesis of amide derivatives from their corresponding amines and 1,3-dicarbonyls.
doi_str_mv 10.1039/d0nj04158k
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Cleavage
Covalent bonds
Derivatives
Functional groups
Substrates
Synthesis
Transition metals
title An organocatalytic C-C bond cleavage approach: a metal-free and peroxide-free facile method for the synthesis of amide derivatives
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