Linked Life Data

10825965

Source:http://linkedlifedata.com/resource/pubmed/id/10825965

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2000-6-20
pubmed:abstractText
[formula: see text] Dienes 2a-e were used to study allylic substituent effects in the ring-closing metathesis reaction (RCM). Both the steric and electronic character of the allylic substituents were found to influence alkene reactivities. Free allylic hydroxyl groups exert a large activating effect on the RCM reaction rates.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1523-7060
pubmed:author
pubmed:issnType
Print
pubmed:day
7
pubmed:volume
1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1123-5
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1999
pubmed:articleTitle
Some allylic substituent effects in ring-closing metathesis reactions: allylic alcohol activation.
pubmed:affiliation
Department of Chemistry, University of Minnesota, Minneapolis 55455, USA. hoye@chem.umn.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.