18662033

Source:http://linkedlifedata.com/resource/pubmed/id/18662033

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002068, umls-concept:C0025663, umls-concept:C1521827
pubmed:issue	17
pubmed:dateCreated	2008-9-1
pubmed:abstractText	The halohydroxylation of 1-cyclopropylallenes would generate two multisubstituted C=C double bonds and at the same time stereoselectively gives 5-halohexa-3,5-dien-1-ols in moderate to good yields. The latter could be transformed into the corresponding alkynyl-substituted conjugated dienes through the further Sonogashira coupling.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Sep
pubmed:issn	1520-6904
pubmed:author	pubmed-author:HuangXianX, pubmed-author:MarxB DBD, pubmed-author:YuLeiL
pubmed:issnType	Electronic
pubmed:day	5
pubmed:volume	73
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	6895-8
pubmed:year	2008
pubmed:articleTitle	Halohydroxylation of 1-cyclopropylallenes: an efficient and stereoselective method for the preparation of multisubstituted olefins.
pubmed:affiliation	Department of Chemistry, Zhejiang University (Xixi Campus), Hangzhou 310028, People's Republic of China.
pubmed:publicationType	Journal Article