17655258

Source:http://linkedlifedata.com/resource/pubmed/id/17655258

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0444498, umls-concept:C0678640, umls-concept:C1524063, umls-concept:C1545588
pubmed:issue	17
pubmed:dateCreated	2007-8-10
pubmed:abstractText	Isopropoxide protection of arylboronates allowed their use in metal-halogen exchange reactions. The isopropoxide-protected borate species were obtained from a boronate or in situ from dibromoarenes. meta- and para-dibromoarenes were converted via these intermediates into functionalized arylboronates in a one-pot manner.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Aug
pubmed:issn	0022-3263
pubmed:author	pubmed-author:QinJiangJ, pubmed-author:RyanMeaganM, pubmed-author:ZhichkinPaulP
pubmed:issnType	Print
pubmed:day	17
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	6618-20
pubmed:year	2007
pubmed:articleTitle	Use of in situ isopropoxide protection in the metal-halogen exchange of arylboronates.
pubmed:affiliation	AMRI, 26 Corporate Circle, P.O. Box 15098, Albany, New York 12212, USA.
pubmed:publicationType	Journal Article