Literature DB >> 21377363

Synthesis of 5-arylated N-arylthiazole-2-amines as potential skeletal muscle cell differentiation promoters.

Michael Schnürch1, Birgit Waldner, Karlheinz Hilber, Marko D Mihovilovic.   

Abstract

A series of N-arylthiazole-2-amines was prepared and their biological activity for the promotion of skeletal muscle cell differentiation was investigated, a process of significant importance in muscle regeneration. A versatile new synthetic route towards the target compounds was developed and the substrate scope of this methodology was investigated. Introduction of the 2-aminoaryl substituent was carried out via nucleophilic substitution reactions in excellent yields. Furthermore, the aryl in 5-position was introduced applying a direct arylation reaction, a major improvement compared to reported synthetic routes regarding atom efficiency and sustainability.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21377363     DOI: 10.1016/j.bmcl.2011.01.123

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  Direct Arylation of Benzo[b]furan and Other Benzo-Fused Heterocycles.

Authors:  Toan Dao-Huy; Maximilian Haider; Fabian Glatz; Michael Schnürch; Marko D Mihovilovic
Journal:  European J Org Chem       Date:  2014-11-17

2.  Mild Pd-catalyzed aminocarbonylation of (hetero)aryl bromides with a palladacycle precatalyst.

Authors:  Stig D Friis; Troels Skrydstrup; Stephen L Buchwald
Journal:  Org Lett       Date:  2014-08-04       Impact factor: 6.005

3.  Gold nanoparticles stabilized with βcyclodextrin-2-amino-4-(4-chlorophenyl)thiazole complex: A novel system for drug transport.

Authors:  I Asela; M Noyong; U Simon; J Andrades-Lagos; J Campanini-Salinas; D Vásquez-Velásquez; M Kogan; N Yutronic; R Sierpe
Journal:  PLoS One       Date:  2017-10-11       Impact factor: 3.240

  3 in total

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