21355584

Source:http://linkedlifedata.com/resource/pubmed/id/21355584

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001383, umls-concept:C0007004, umls-concept:C0243072
pubmed:issue	11
pubmed:dateCreated	2011-3-17
pubmed:abstractText	Reversible covalent interactions of organoboron compounds are exploited as the basis for regioselective borinic acid-catalyzed acylations of polyols. This catalytic protocol enables differentiation of the secondary OH groups of a wide range of carbohydrate derivatives with diverse acid chloride and chloroformate reagents, using a structurally simple diarylborinic acid-derived catalyst.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7503056
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Mar
pubmed:issn	1520-5126
pubmed:author	pubmed-author:LeeDorisD, pubmed-author:TaylorMark SMS
pubmed:issnType	Electronic
pubmed:day	23
pubmed:volume	133
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3724-7
pubmed:year	2011
pubmed:articleTitle	Borinic acid-catalyzed regioselective acylation of carbohydrate derivatives.
pubmed:affiliation	Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.
pubmed:publicationType	Journal Article