Linked Life Data

21456515

Source:http://linkedlifedata.com/resource/pubmed/id/21456515

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2011-4-29
pubmed:abstractText
A rapid approach to the spirocyclic core of cyclopamine was achieved in four steps from 2-pentenyl-furan. A furan Diels-Alder reaction followed by a one-pot dehalogenation/amination sequence provides the oxabicyclic triene that upon treatment with Grubbs' catalyst undergoes smooth rearrangement to the tricyclic core.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1523-7052
pubmed:author
pubmed:issnType
Electronic
pubmed:day
6
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2433-5
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Tandem metathesis reactions of oxabicyclo[2.2.1]heptenes: studies on the spirocyclic core of cyclopamine.
pubmed:affiliation
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, Connecticut 06269, United States.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S.