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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
14
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pubmed:dateCreated |
2008-7-11
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pubmed:abstractText |
A selective and efficient method for the synthesis of 3-(1-arylmethylene)oxindoles by palladium-catalyzed C-H functionalization of anilides with aryliodonium salts has been developed. In the presence of Pd(OAc)2 and Et3N, a variety of anilides underwent the reaction with aryliodonium salts to afford the corresponding 3-(1-arylmethylene)oxindoles in moderate to good yields. It is noteworthy that the reaction can be conducted providing moderate yields even without bases. The mechanism of the reaction was also discussed.
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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 |
Jul
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pubmed:issn |
1520-6904
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:day |
18
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5476-80
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pubmed:meshHeading |
|
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pubmed:year |
2008
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pubmed:articleTitle |
Palladium-catalyzed C-H functionalization of N-arylpropiolamides with aryliodonium salts: selective synthesis of 3-(1-arylmethylene)oxindoles.
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|
pubmed:affiliation |
Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research (Ministry of Education), Hunan Normal University, Changsha 410081, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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