12240246

Source:http://linkedlifedata.com/resource/pubmed/id/12240246

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0043047, umls-concept:C0074728, umls-concept:C0220781, umls-concept:C0332514, umls-concept:C1704241, umls-concept:C1883254
pubmed:issue	19
pubmed:dateCreated	2002-9-20
pubmed:abstractText	beta-Cyclodextrin catalyses for the first time the asymmetric reduction of alpha-azido aryl ketones to corresponding alcohols of great significance using sodium borohydride in water. The azido group appeared to be the best fit among various groups studied. This asymmetric reduction using water as solvent overcomes many of the drawbacks in the existing methodologies.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	1359-7345
pubmed:author	pubmed-author:BhanumathiNN, pubmed-author:RaoK RKR, pubmed-author:ReddyM AMA
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1974-5
pubmed:dateRevised	2003-11-3
pubmed:year	2001
pubmed:articleTitle	Asymmetric synthesis of 2-azido-1-arylethanols from azido aryl ketone-beta-cyclodextrin complexes and sodium borohydride in water.
pubmed:affiliation	Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India.
pubmed:publicationType	Journal Article