12790552

Source:http://linkedlifedata.com/resource/pubmed/id/12790552

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:C0014898, umls-concept:C0034326, umls-concept:C0035973, umls-concept:C0220781, umls-concept:C0443286, umls-concept:C0597695, umls-concept:C0598128, umls-concept:C1522492, umls-concept:C1707310, umls-concept:C1723692, umls-concept:C1883254
pubmed:issue	12
pubmed:dateCreated	2003-6-6
pubmed:abstractText	[reaction: see text] Ruthenium porphyrins catalyze three-component coupling reaction of alpha-diazo esters with a series of N-benzylidene imines and alkenes to form functionalized pyrrolidines in excellent diastereoselectivities. The reaction proceeds via a reactive ruthenium-carbene intermediate and its subsequent reaction with imine to generate azomethine ylide, which reacts with alkenes via 1,3-diploar cycloaddition.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jun
pubmed:issn	1523-7060
pubmed:author	pubmed-author:CheChi-MingCM, pubmed-author:ChenJianJ, pubmed-author:HongWeiW, pubmed-author:LiGong-YongGY, pubmed-author:YuWing-YiuWY
pubmed:issnType	Print
pubmed:day	12
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2153-6
pubmed:year	2003
pubmed:articleTitle	Stereoselective synthesis of functionalized pyrrolidines by ruthenium porphyrin-catalyzed decomposition of alpha-diazo esters and cascade azomethine ylide formation/1,3-dipolar cycloaddition reactions.
pubmed:affiliation	Shanghai-Hong Kong Joint Laboratory on Chemical Synthesis, Shanghai Institute of Organic Chemistry, The Chinese Academy of Sciences, 354 Feng Lin Road, Shanghai 200032, China.
pubmed:publicationType	Journal Article