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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
21
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pubmed:dateCreated |
2010-10-14
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pubmed:abstractText |
A strategy involving palladium-catalyzed cyclization of halo-phenyl hydrazones and aryl isocyanates provides a convenient approach to the synthesis of 1,3,4-benzotriazepines (4) or 1-arylamide-1H-indazoles (5) in good isolated yields. Microwave irradiation was found to afford high reaction efficiency, while the choice of halophenyl hydrazone had an effect on the pathway of the reaction.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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|
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1477-0539
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:day |
7
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4827-30
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pubmed:meshHeading |
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pubmed:year |
2010
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pubmed:articleTitle |
Facile synthesis of 1,3,4-benzotriazepines and 1-arylamide-1H-indazoles via palladium-catalyzed cyclization of aryl isocyanates and aryl hydrazones under microwave irradiation.
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|
pubmed:affiliation |
College of Pharmacy, State Key Laboratory of Virology, Wuhan University, Wuhan, 430071, China. cdong@whu.edu.cn
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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