Literature DB >> 24650172

Role of linkers in tertiary amines that mediate or catalyze 1,3,5-triazine-based amide-forming reactions.

Masanori Kitamura1, Fumitaka Kawasaki, Kouichi Ogawa, Shuichi Nakanishi, Hiroyuki Tanaka, Kohei Yamada, Munetaka Kunishima.   

Abstract

We studied 1,3,5-triazine-based amide-forming reactions that are mediated or catalyzed by various tert-amines. The representative tert-amine was trimethylamine, which has amido, 1,2,3-triazolyl, aryl, and alkyl linkers. It was found that electron-deficient aryl and heteroaryl linkers, particularly 1,2,3-triazolyl linkers, are superior. On the basis of our findings, we synthesized ligand catalysts, including a 1,2,3-triazolyl linker that connects a protein ligand to a trimethylamine moiety, and found that fluorescent-labeling of a targeting protein using the ligand catalysts proceeded in good yields.

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Year:  2014        PMID: 24650172     DOI: 10.1021/jo500376m

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

Review 1.  Catalytic and non-catalytic amidation of carboxylic acid substrates.

Authors:  Keyvan Pedrood; Saeed Bahadorikhalili; Vahid Lotfi; Bagher Larijani; Mohammad Mahdavi
Journal:  Mol Divers       Date:  2021-06-13       Impact factor: 2.943

2.  Potent triazine-based dehydrocondensing reagents substituted by an amido group.

Authors:  Munetaka Kunishima; Daiki Kato; Nobu Kimura; Masanori Kitamura; Kohei Yamada; Kazuhito Hioki
Journal:  Beilstein J Org Chem       Date:  2016-08-24       Impact factor: 2.883

  2 in total

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