14737566

Source:http://linkedlifedata.com/resource/pubmed/id/14737566

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0185125, umls-concept:C0332219, umls-concept:C0443286, umls-concept:C1521827, umls-concept:C1710236, umls-concept:C1883254
pubmed:issue	2
pubmed:dateCreated	2004-1-22
pubmed:abstractText	We have developed a general and highly efficient method for the preparation of diverse [small omega]-formyl-[small alpha],[small beta]-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologically important polycyclic compounds.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jan
pubmed:issn	1359-7345
pubmed:author	pubmed-author:KimHee JinHJ, pubmed-author:KooSanghoS, pubmed-author:YangXiulingX, pubmed-author:YeoJung EunJE
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	236-7
pubmed:year	2004
pubmed:articleTitle	The intramolecular Baylis-Hillman reaction: easy preparation of versatile substrates, facile reactions, and synthetic applications.
pubmed:affiliation	Department of Chemistry, Myong Ji University, Yongin, Kyunggi-Do, 449-728, Korea.
pubmed:publicationType	Journal Article