16468756

Source:http://linkedlifedata.com/resource/pubmed/id/16468756

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002505, umls-concept:C0020276, umls-concept:C0022634, umls-concept:C0439851, umls-concept:C1552596, umls-concept:C1947931
pubmed:issue	4
pubmed:dateCreated	2006-2-10
pubmed:abstractText	[reaction: see text] A novel, biomimetic concept for the direct reductive amination of ketones is described that relies on selective imine activation by hydrogen bond formation. The mild, acid- and metal-free process requires only catalytic amounts of thiourea as hydrogen bond donor and utilizes the Hantzsch ester for transfer hydrogenation. The method allows the efficient synthesis of structurally diverse amines.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	1523-7060
pubmed:author	pubmed-author:HassfeldJormaJ, pubmed-author:MeeSS, pubmed-author:MencheDirkD, pubmed-author:MencheGerdG, pubmed-author:RitterAntjeA, pubmed-author:RudolphSvenS
pubmed:issnType	Print
pubmed:day	16
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	741-4
pubmed:year	2006
pubmed:articleTitle	Hydrogen bond catalyzed direct reductive amination of ketones.
pubmed:affiliation	Gesellschaft für Biotechnologische Forschung mbH, Medzinische Chemie, Mascheroder Weg 1, D-38124 Braunschweig, Germany. dme05@gbf.de
pubmed:publicationType	Journal Article