15101748

Source:http://linkedlifedata.com/resource/pubmed/id/15101748

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001975, umls-concept:C0449445, umls-concept:C0682996, umls-concept:C1101375
pubmed:issue	9
pubmed:dateCreated	2004-4-22
pubmed:abstractText	[reaction: see text] Allyl, isopentenyl, geranyl, citronellyl, farnesyl, and phytyl alcohols were transformed in good yield (>60%) into their phosphorothioates via a DBU-assisted 1,3,2-oxathiaphospholane ring-opening condensation with 2-(2-cyanoethoxy)-2-thiono-1,3,2-oxathiaphospholane, a reagent that is stable and easy to handle, followed by subsequent removal of the 2-cyanoethyl group from the intermediate phosphorothioate diester under basic conditions.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Apr
pubmed:issn	1523-7060
pubmed:author	pubmed-author:ChojnackiTadeuszT, pubmed-author:NawrotBarbaraB, pubmed-author:StecWojciech JWJ, pubmed-author:ZmudzkaKatarzynaK
pubmed:issnType	Print
pubmed:day	29
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1385-7
pubmed:year	2004
pubmed:articleTitle	An oxathiaphospholane approach to one-pot phosphorothioylation of isoprenoid alcohols.
pubmed:affiliation	Department of Bioorganic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland.
pubmed:publicationType	Journal Article