Literature DB >> 15080974

Highly diastereoselective inverse electron demand (IED) Diels-Alder reaction mediated by chiral salen-AlCl complex: the first, target-oriented synthesis of pyranoquinolines as potential antibacterial agents.

Chinnian J Magesh1, Sarasu V Makesh, Paramasivan T Perumal.   

Abstract

The first, target-oriented synthesis of pyranoquinolines as potential antibacterial agents by inverse electron demand (IED) Diels-Alder reaction using chiral salen-AlCl complex has been accomplished, the reactions proceed with moderate yields, and a very high degree of diastereoselectivity (>90%). The diastereoselectivity-enhanced pyranoquinolines exhibit potential bactericidal activity against seven strains of pathogenic gram-negative bacteria.

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Year:  2004        PMID: 15080974     DOI: 10.1016/j.bmcl.2004.02.057

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


  3 in total

1.  A luminescent aluminium salen complex allows for monitoring dynamic vesicle trafficking from the Golgi apparatus to lysosomes in living cells.

Authors:  Juan Tang; Hao-Yan Yin; Jun-Long Zhang
Journal:  Chem Sci       Date:  2018-01-08       Impact factor: 9.825

2.  Synthesis and Antimicrobial Activity of some Tetrahydro Quinolone Diones and Pyrano[2,3-d]pyrimidine Derivatives.

Authors:  Masoume Shahi; Naser Foroughifar; Akbar Mobinikhaledi
Journal:  Iran J Pharm Res       Date:  2015       Impact factor: 1.696

3.  Synthesis of hexahydrofuro[3,2-c]quinoline, a martinelline type analogue and investigation of its biological activity.

Authors:  P-Y Chung; J C-O Tang; C-H Cheng; Z-X Bian; W-Y Wong; K-H Lam; C-H Chui
Journal:  Springerplus       Date:  2016-03-03
  3 in total

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