15228290

Source:http://linkedlifedata.com/resource/pubmed/id/15228290

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:C0035973, umls-concept:C0678615, umls-concept:C0772162
pubmed:issue	14
pubmed:dateCreated	2004-7-1
pubmed:abstractText	[reaction: see text] Ruthenium(II) porphyrin-catalyzed amidation of aromatic heterocycles with iminoiodanes under mild conditions (CH(2)Cl(2), 4 A molecular sieves, ultrasound, 40 degrees C) was achieved in moderate to good yields (up to 84%) and conversions (up to 99%). Only the N,N-ditosylamidated product was obtained for reactions involving heteroarenes, where X = O, S, or NTs. N-Alkyl- and N-aryl-substituted pyrroles, on the other hand, were shown to give the 3,4-diaminated adduct.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1523-7060
pubmed:author	pubmed-author:ChanPhilip Wai HongPW, pubmed-author:CheChi-MingCM, pubmed-author:HeLingL, pubmed-author:TsuiWai-ManWM, pubmed-author:YuWing-YiuWY
pubmed:issnType	Print
pubmed:day	8
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2405-8
pubmed:year	2004
pubmed:articleTitle	Ruthenium(II) porphyrin-catalyzed amidation of aromatic heterocycles.
pubmed:affiliation	Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.
pubmed:publicationType	Journal Article