Source:http://linkedlifedata.com/resource/pubmed/id/16880718
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2006-8-1
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pubmed:abstractText |
Novel fluoroalkylated products where a CF(2)COOEt group was introduced at the alpha-position of alpha,beta-unsaturated ketones or the Reformatsky-type products have been obtained selectively by the reaction of BrCF(2)COOEt and alpha,beta-unsaturated ketones with Et(2)Zn in the presence of RhCl(PPh(3))(3) depending on the solvents. Furthermore, the novel alpha-fluoroalkylated products could synthesize by using various halofluoroalkyl compounds (R(f)-X) instead of BrCF(2)COOEt. On the other hand, this Reformatsky-type reaction by imines gave difluoro-beta-lactams or 3-amino-2,2-difluorocalboxylic esters without or with MgSO(4) . 7H(2)O, selectively.
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pubmed:language |
jpn
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0031-6903
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
126
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
597-605
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16880718-Alkylation,
pubmed-meshheading:16880718-Catalysis,
pubmed-meshheading:16880718-Chemistry, Organic,
pubmed-meshheading:16880718-Fluorine Compounds,
pubmed-meshheading:16880718-Methylation,
pubmed-meshheading:16880718-Organic Chemistry Phenomena,
pubmed-meshheading:16880718-Rhodium
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pubmed:year |
2006
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pubmed:articleTitle |
[Development of new reactions of fluorine compounds using a rhodium catalyst].
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pubmed:affiliation |
Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata City, Japan. sato@pharm.setsunan.ac.jp
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pubmed:publicationType |
Journal Article,
English Abstract,
Review
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