12375892

Source:http://linkedlifedata.com/resource/pubmed/id/12375892

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205352, umls-concept:C0220781, umls-concept:C0443286, umls-concept:C0596258, umls-concept:C0761982, umls-concept:C1710028, umls-concept:C1883254
pubmed:issue	21
pubmed:dateCreated	2002-10-11
pubmed:abstractText	[reaction: see text] The reaction of nitroso compounds with enolates, "the nitroso aldol reaction", occurs in high yield to generate alpha-hydroxyamino carbonyl compounds. Yields range from 42% to 98% with N-selectivity >99:1 from commercially available aromatic or aliphatic nitroso compounds and a variety of alkali metal or tin enolates.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	1523-7060
pubmed:author	pubmed-author:MomiyamaNorieN, pubmed-author:YamamotoHisashiH
pubmed:issnType	Print
pubmed:day	17
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3579-82
pubmed:dateRevised	2003-11-3
pubmed:year	2002
pubmed:articleTitle	Simple synthesis of alpha-hydroxyamino carbonyl compounds: new scope of the nitroso aldol reaction.
pubmed:affiliation	Graduate School of Engineering, Nagoya University, SORST, Japan Science and Technology Corporation (JST), Chikusa, Nagoya 464-8603, Japan.
pubmed:publicationType	Journal Article