Source:http://linkedlifedata.com/resource/pubmed/id/15599460
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
|
pubmed:dateCreated |
2004-12-15
|
pubmed:abstractText |
Exposure of 1-alkynyl[p-(trifluoromethyl)phenyl](tetrafluoroborato)-lambda(3)-bromanes to sodium benzenesulfinate or sodium trifluoromethanesulfinate in dichloromethane at 0 degree C under argon resulted in tandem Michael-carbene insertion reactions to produce 1-sulfonylcyclopentenes selectively, with concomitant formation of a small amount of rearranged 1-alkynyl sulfones.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1359-7345
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
21
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2894-5
|
pubmed:year |
2004
|
pubmed:articleTitle |
Tandem Michael addition-carbene insertion reaction of 1-alkynyl(aryl)(tetrafluoroborato)-lambda3-bromanes: 1-(phenylsulfonyl)- and 1-(trifluoromethylsulfonyl)cyclopentene annulation.
|
pubmed:affiliation |
Faculty of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan. mochiai@ph.tokushima-u.ac.jp
|
pubmed:publicationType |
Journal Article
|