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Article: Enantioselective intramolecular amidation of sulfamate esters catalyzed by chiral manganese(III) Schiff-base complexes

TitleEnantioselective intramolecular amidation of sulfamate esters catalyzed by chiral manganese(III) Schiff-base complexes
Authors
Issue Date2005
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2005, v. 46 n. 32, p. 5403-5408 How to Cite?
AbstractEnantioselective intramolecular amidation of sulfamate esters catalyzed by chiral manganese(III) Schiff-base complexes under mild conditions (PhI(OAc) 2, Al 2O 3, C 6H 6, 5°C) was achieved in moderate to good yields (up to 92%), substrate conversions (up to 99%), with virtually complete cis-selectivity and with ee values up to 79% ee. © 2005 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/68847
ISSN
2015 Impact Factor: 2.347
2015 SCImago Journal Rankings: 0.782
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhang, Jen_HK
dc.contributor.authorChan, PWHen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:08:16Z-
dc.date.available2010-09-06T06:08:16Z-
dc.date.issued2005en_HK
dc.identifier.citationTetrahedron Letters, 2005, v. 46 n. 32, p. 5403-5408en_HK
dc.identifier.issn0040-4039en_HK
dc.identifier.urihttp://hdl.handle.net/10722/68847-
dc.description.abstractEnantioselective intramolecular amidation of sulfamate esters catalyzed by chiral manganese(III) Schiff-base complexes under mild conditions (PhI(OAc) 2, Al 2O 3, C 6H 6, 5°C) was achieved in moderate to good yields (up to 92%), substrate conversions (up to 99%), with virtually complete cis-selectivity and with ee values up to 79% ee. © 2005 Elsevier Ltd. All rights reserved.en_HK
dc.languageengen_HK
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetleten_HK
dc.relation.ispartofTetrahedron Lettersen_HK
dc.titleEnantioselective intramolecular amidation of sulfamate esters catalyzed by chiral manganese(III) Schiff-base complexesen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0040-4039&volume=46&spage=5403&epage=5408&date=2005&atitle=Enantioselective+intramolecular+amidation+of+sulfamate+esters+catalyzed+by+chiral+manganese+(III)+Schiff-base+complexesen_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.tetlet.2005.05.146en_HK
dc.identifier.scopuseid_2-s2.0-21844463306en_HK
dc.identifier.hkuros117767en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-21844463306&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume46en_HK
dc.identifier.issue32en_HK
dc.identifier.spage5403en_HK
dc.identifier.epage5408en_HK
dc.identifier.isiWOS:000230685900035-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridZhang, J=7601356154en_HK
dc.identifier.scopusauthoridChan, PWH=13607033800en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK

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