10549145

Source:http://linkedlifedata.com/resource/pubmed/id/10549145

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0035548, umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	9
pubmed:dateCreated	1999-11-23
pubmed:abstractText	The carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring beta-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the heterocycles, appropriately protected where necessary, with a differentially protected, chiral carbocyclic core.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/GM46243
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8215930
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleosides, http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleotides
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0732-8311
pubmed:author	pubmed-author:AntleV DVD, pubmed-author:CaperelliC ACA
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1911-28
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:10549145-Molecular Conformation, pubmed-meshheading:10549145-Molecular Structure, pubmed-meshheading:10549145-Ribonucleosides, pubmed-meshheading:10549145-Ribonucleotides
pubmed:year	1999
pubmed:articleTitle	Synthesis of chiral carbocyclic ribonucleotides.
pubmed:affiliation	Division of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati Medical Center, OH 45267-0004, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S.