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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2009-6-11
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pubmed:abstractText |
A variety of substituted enamine derivatives were first found to be conveniently converted to the corresponding 2H-azirines mediated by phenyliodine (III) diacetate (PIDA). The formed 2-aryl-2H-azirines could be applied in the synthesis of indole-3-carbonitriles or isoxazoles via thermal rearrangements.
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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 |
Jun
|
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pubmed:issn |
1523-7052
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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 |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2643-6
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pubmed:meshHeading |
pubmed-meshheading:19438258-Azirines,
pubmed-meshheading:19438258-Biphenyl Compounds,
pubmed-meshheading:19438258-Crystallography, X-Ray,
pubmed-meshheading:19438258-Cyclization,
pubmed-meshheading:19438258-Differential Thermal Analysis,
pubmed-meshheading:19438258-Imidazoles,
pubmed-meshheading:19438258-Indoles,
pubmed-meshheading:19438258-Isoxazoles,
pubmed-meshheading:19438258-Molecular Structure,
pubmed-meshheading:19438258-Nitriles,
pubmed-meshheading:19438258-Stereoisomerism,
pubmed-meshheading:19438258-Structure-Activity Relationship
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pubmed:year |
2009
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pubmed:articleTitle |
Simple conversion of enamines to 2H-azirines and their rearrangements under thermal conditions.
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pubmed:affiliation |
Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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