12120400

Source:http://linkedlifedata.com/resource/pubmed/id/12120400

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0034760, umls-concept:C0522529, umls-concept:C0917735, umls-concept:C1521827, umls-concept:C1720952
pubmed:issue	3
pubmed:dateCreated	2002-7-17
pubmed:abstractText	Conjugated diynes underwent selective mono-titanation with a Ti(II) reagent to give 1:1 diyne-titanium alkoxide complexes, which reacted with proton, aldehyde, and another acetylene to give stereo-defined enynes, enynols, and dienynes.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	1359-7345
pubmed:author	pubmed-author:DelasChristopheC, pubmed-author:IlligJ JJJ, pubmed-author:UrabeHirokazuH
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	272-3
pubmed:dateRevised	2003-11-3
pubmed:year	2002
pubmed:articleTitle	Site-selective mono-titanation of conjugated diynes with a Ti(II) alkoxide reagent. Concise preparation of stereo-defined enynes and dienynes.
pubmed:affiliation	Department of Biomolecular Engineering, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8501, Japan.
pubmed:publicationType	Journal Article