Source:http://linkedlifedata.com/resource/pubmed/id/11418031
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
2001-6-21
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pubmed:abstractText |
[reaction: see text] Adjacent tris(cyclic ethers) and enol ethers have been synthesized in good yields for the first time via a triple olefin metathesis reaction using Grubbs' catalyst RuCl(2)(=C(H)Ph)(PCy(3))(2) (Cy = cyclohexyl), and the 1,3-dimesitylimidazol-2-ylidene ruthenium benzylidene catalyst RuCl(2)(=C(H)Ph)(PCy(3))(IMes) ((IMes) = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene). The latter proved to be the most efficient catalyst in these transformations.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1989-91
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pubmed:dateRevised |
2003-10-31
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pubmed:year |
2001
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pubmed:articleTitle |
Triple ring closing metathesis reaction: synthesis of adjacent cyclic ethers.
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pubmed:affiliation |
CEA-CE Saclay, Service des Molécules Marquées, Bât 547, Département de Biologie Cellulaire et Moléculaire, F-91191 Gif sur Yvette cedex, France. heck@dsvidf.cea.fr
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pubmed:publicationType |
Journal Article
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