12520501

Source:http://linkedlifedata.com/resource/pubmed/id/12520501

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0215830, umls-concept:C0332282, umls-concept:C0332514, umls-concept:C1511695
pubmed:issue	2
pubmed:dateCreated	2003-1-9
pubmed:abstractText	(OC)Ru(salen) 1 was found to catalyze sulfimidation of alkyl aryl sulfides in the presence of arylsulfonyl azide with high enantioselectivity, up to 99% ee. When the substrates were allylic sulfides, the resulting sulfimides underwent [2,3]sigmatropic rearrangement to give the corresponding N-allyl toluenesulsulfonamides with greater than 80% ee.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8914261
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	0899-0042
pubmed:author	pubmed-author:KatsukiTsutomuT, pubmed-author:MurakamiMasakazuM, pubmed-author:SaitoBunnaiB, pubmed-author:UchidaTatsuyaT
pubmed:copyrightInfo	Copyright 2003 Wiley-Liss, Inc.
pubmed:issnType	Print
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	116-23
pubmed:dateRevised	2003-11-4
pubmed:year	2003
pubmed:articleTitle	Ru(salen)-catalyzed asymmetric sulfimidation and subsequent [2,3]sigmatropic rearrangement.
pubmed:affiliation	Department of Chemistry, Faculty of Science, Graduate School, Kyushu University 33, CREST, JST (Japan Science and Technology), Higashi-ku, Fukuoka 812-8581, Japan.
pubmed:publicationType	Journal Article