16886081

Source:http://linkedlifedata.com/resource/pubmed/id/16886081

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030957, umls-concept:C0040877, umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	16
pubmed:dateCreated	2006-8-3
pubmed:abstractText	The product of an episulfonium ion-mediated cyclotrimerisation, previously reported as being a 15-membered ring trilactam, has now been shown to be a 1,3,5-triazine. Smaller medium-ring bilactams have, however, been synthesised from linear precursors using the sulfur-based methodology.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101154995
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Peptides, Cyclic, http://linkedlifedata.com/resource/pubmed/chemical/Sulfonium Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Triazines
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1477-0520
pubmed:author	pubmed-author:FoxDavid JDJ, pubmed-author:MorleyThomas JTJ, pubmed-author:WarrenStuartS
pubmed:issnType	Print
pubmed:day	21
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3120-4
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:16886081-Peptides, Cyclic, pubmed-meshheading:16886081-Sulfonium Compounds, pubmed-meshheading:16886081-Triazines
pubmed:year	2006
pubmed:articleTitle	Episulfonium ion-mediated cyclic peptide and triazine synthesis.
pubmed:affiliation	University Chemical Laboratory, Lensfield Road, Cambridge, UK. djf34@cam.ac.uk
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't