Source:http://linkedlifedata.com/resource/pubmed/id/19647904
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2009-10-9
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pubmed:abstractText |
2-Chloro-5-methylpyridine-3-olefin derivatives (3a-e) have been synthesized from 2-chloro-5-methylnicotinaldehyde (1) and studied their photochemical E (trans)-->Z (cis) isomerization upon direct irradiation and triplet sensitized excitation for the first time. The triplet sensitized excitations of the compounds yielded high Z (4a-e) isomer composition, whereas the direct excitation results in less Z (4a-e) isomer composition, indicating triplet pathway is very efficient in converting the E (trans)-->Z (cis) isomer. Thus synthesized E (3a-c and 3e) and generated Z (4a-c and 4e) isomers were tested for antimicrobial activity. Antifungal activity of these pyridine derivatives are closely comparable to the standard used.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1768-3254
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4661-7
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pubmed:meshHeading |
pubmed-meshheading:19647904-Alkenes,
pubmed-meshheading:19647904-Anti-Infective Agents,
pubmed-meshheading:19647904-Bacteria,
pubmed-meshheading:19647904-Fungi,
pubmed-meshheading:19647904-Isomerism,
pubmed-meshheading:19647904-Photochemistry,
pubmed-meshheading:19647904-Pyridines,
pubmed-meshheading:19647904-Structure-Activity Relationship
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pubmed:year |
2009
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pubmed:articleTitle |
Synthesis, photochemical E (trans)-->Z (cis) isomerization and antimicrobial activity of 2-chloro-5-methylpyridine-3-olefin derivatives.
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pubmed:affiliation |
Organic Chemistry Division-II, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500 607, India.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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