12839469

Source:http://linkedlifedata.com/resource/pubmed/id/12839469

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0598128, umls-concept:C1883254
pubmed:issue	14
pubmed:dateCreated	2003-7-3
pubmed:abstractText	Enynes 5a-g were prepared in moderate to good yields from 1-(triphenylphosphoranylideneaminoalkyl)benzotriazoles. Ring-closing metathesis of 5a-f afforded functionalized dienes 6a-f, respectively, which were used in a Diels-Alder cycloaddition reaction in the synthesis of the corresponding hexahydroisoquinoline derivatives 7a-f.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	0022-3263
pubmed:author	pubmed-author:AkhmedovNovruz GNG, pubmed-author:KatritzkyAlan RAR, pubmed-author:KhokhlovaTatyanaT, pubmed-author:NairSatheesh KSK
pubmed:issnType	Print
pubmed:day	11
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5724-7
pubmed:year	2003
pubmed:articleTitle	Efficient synthesis of enynecarbamates and their ring-closing metathesis/[4 + 2] Diels-Alder cycloaddition: synthesis of hexahydroisoquinolines.
pubmed:affiliation	Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, USA. katritzky@chem.ufl.edu
pubmed:publicationType	Journal Article