Literature DB >> 25065781

One-pot decarboxylative acylation of N-, O-, S-nucleophiles and peptides with 2,2-disubstituted malonic acids.

Iryna O Lebedyeva1, Suvendu Biswas, Kevin Goncalves, Sean M Sileno, Ashton R Jackson, Kunal Patel, Peter J Steel, Alan R Katritzky.   

Abstract

Monocarbonyl activation of 2,2-disubstituted malonic acids with benzotriazole leads to decarboxylation of one of the carboxy groups and formation of a CH bond. Intermediate carbonyl benzotriazoles then readily acylate nucleophilic reagents and peptides resulting in libraries of conjugates and peptidomimetics.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  acylation; cleavage reactions; conjugates; decarboxylation; peptides

Year:  2014        PMID: 25065781     DOI: 10.1002/chem.201403529

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

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Authors:  Tony Fröhlich; Christoph Reiter; Mohamed E M Saeed; Corina Hutterer; Friedrich Hahn; Maria Leidenberger; Oliver Friedrich; Barbara Kappes; Manfred Marschall; Thomas Efferth; Svetlana B Tsogoeva
Journal:  ACS Med Chem Lett       Date:  2017-12-21       Impact factor: 4.345

2.  Highly selective acylation of polyamines and aminoglycosides by 5-acyl-5-phenyl-1,5-dihydro-4H-pyrazol-4-ones.

Authors:  Kostiantyn O Marichev; Estevan C Garcia; Kartick C Bhowmick; Daniel J Wherritt; Hadi Arman; Michael P Doyle
Journal:  Chem Sci       Date:  2017-08-30       Impact factor: 9.825

  2 in total

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