Literature DB >> 34120303

Catalytic and non-catalytic amidation of carboxylic acid substrates.

Keyvan Pedrood1, Saeed Bahadorikhalili2, Vahid Lotfi2, Bagher Larijani1, Mohammad Mahdavi3.   

Abstract

The present review offers an apt summary of amide bond formation with carboxylic acid substrates by taking advantage of several methods. Carboxamides can be regarded as a substantial part of organic and medicinal chemistry due to their utility in synthesizing peptides, lactams, and more than 25% of familiar drugs. Moreover, they play a leading role in the synthesis of bioactive products with anticancer, antifungal, and antibacterial properties. The data are arranged based on the type and amount of reagents used to conduct amidation and are also divided into the following categories: catalytic amidation of carboxylic acids, non-catalytic amidation, and transamidation.
© 2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Entities:  

Keywords:  Amidation; Carboxylic acid; Catalytic; Non-catalytic; Transamidation

Mesh:

Substances:

Year:  2021        PMID: 34120303     DOI: 10.1007/s11030-021-10252-0

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  33 in total

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2.  Silica gel-mediated amide bond formation: an environmentally benign method for liquid-phase synthesis and cytotoxic activities of amides.

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Journal:  J Comb Chem       Date:  2010-05-10

3.  Direct Amidation of Carboxylic Acids through an Active α-Acyl Enol Ester Intermediate.

Authors:  Xianjun Xu; Huangdi Feng; Liliang Huang; Xiaohui Liu
Journal:  J Org Chem       Date:  2018-06-11       Impact factor: 4.354

4.  Direct Conversion of Carboxylic Acids to Various Nitrogen-Containing Compounds in the One-Pot Exploiting Curtius Rearrangement.

Authors:  Arun Kumar; Naveen Kumar; Ritika Sharma; Gaurav Bhargava; Dinesh Mahajan
Journal:  J Org Chem       Date:  2019-08-21       Impact factor: 4.354

5.  Borate esters as convenient reagents for direct amidation of carboxylic acids and transamidation of primary amides.

Authors:  Pavel Starkov; Tom D Sheppard
Journal:  Org Biomol Chem       Date:  2011-01-06       Impact factor: 3.876

6.  Recent Developments in Amide Synthesis Using Nonactivated Starting Materials.

Authors:  Andrea Ojeda-Porras; Diego Gamba-Sánchez
Journal:  J Org Chem       Date:  2016-11-15       Impact factor: 4.354

7.  Catalytic amide formation from non-activated carboxylic acids and amines.

Authors:  Helena Lundberg; Fredrik Tinnis; Nicklas Selander; Hans Adolfsson
Journal:  Chem Soc Rev       Date:  2014-01-15       Impact factor: 54.564

8.  The interaction of ammonium, sulfonium, and sulfide analogues of metoclopramide with the dopamine D2 receptor.

Authors:  M W Harrold; A Sriburi; K Matsumoto; D D Miller; T Farooqui; N Uretsky
Journal:  J Med Chem       Date:  1993-10-15       Impact factor: 7.446

9.  Chemoselective reductions of nitroaromatics in water at room temperature.

Authors:  Sean M Kelly; Bruce H Lipshutz
Journal:  Org Lett       Date:  2013-12-16       Impact factor: 6.005

Review 10.  Amide bond formation: beyond the myth of coupling reagents.

Authors:  Eric Valeur; Mark Bradley
Journal:  Chem Soc Rev       Date:  2008-12-04       Impact factor: 54.564

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  1 in total

1.  Methyltrimethoxysilane (MTM) as a Reagent for Direct Amidation of Carboxylic Acids.

Authors:  D Christopher Braddock; Joshua J Davies; Paul D Lickiss
Journal:  Org Lett       Date:  2022-01-27       Impact factor: 6.005

  1 in total

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