Piperidine-mediated synthesis of thiazolyl chalcones and their derivatives as potent antimicrobial agents.

Abstract:

:A series of new thiazolyl chalcones, 1-[2-amino-4-methyl-1,3-thiazol-5-yl]-3-aryl-prop-2-en-1-one were prepared by piperidine mediated Claisen-Schmidt condensation of thiazolyl ketone with aromatic aldehyde. These chalcones on cyclisation gave 2-amino-6-(2-amino-4-methyl-1,3-thiazol-5-yl)-4-aryl-4H-pyridine-3-carbonitrile and 2-amino-6-(2-amino-4-methyl-1,3-thiazol-5-yl)-4-aryl-4H-pyran-3-carbonitrile. The result showed that the compounds exhibited marked potency as antimicrobial agents.

journal_name

Nat Prod Res

journal_title

Natural product research

authors

Venkatesan P,Maruthavanan T

doi

10.1080/14786419.2010.536161

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

223-34

issue

3

eissn

1478-6419

issn

1478-6427

journal_volume

26

pub_type

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