20162166

Source:http://linkedlifedata.com/resource/pubmed/id/20162166

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0185125, umls-concept:C0596311, umls-concept:C1257890, umls-concept:C1330957, umls-concept:C1707689
pubmed:issue	9
pubmed:dateCreated	2010-2-17
pubmed:abstractText	A new photolabile hydroxyl-protecting group has been developed by introducing a dimethylamino group to the meta position of an aromatic ring of the traditional trityl (Tr) protecting group.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Mar
pubmed:issn	1364-548X
pubmed:author	pubmed-author:LiangXingX, pubmed-author:WangPengfeiP, pubmed-author:ZhangXinX, pubmed-author:ZhouLeiL
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	46
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1514-6
pubmed:year	2010
pubmed:articleTitle	Facilitated photochemical cleavage of benzylic C-O bond. Application to photolabile hydroxyl-protecting group design.
pubmed:affiliation	wangp@uab.edu
pubmed:publicationType	Journal Article