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Article: Ruthenium-catalyzed one-pot carbenoid N-H insertion reactions and diastereoselective synthesis of prolines

TitleRuthenium-catalyzed one-pot carbenoid N-H insertion reactions and diastereoselective synthesis of prolines
Authors
Deng, QHXu, HWYuen, AWHXu, ZJChe, CM
Issue Date2008
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2008, v. 10 n. 8, p. 1529-1532 How to Cite?
DOI: http://dx.doi.org/10.1021/ol800087p
AbstractAryl- and aliphatic-substituted 3-hydroxyprolines and various other amino esters are conveniently prepared by [RuCI2(p-cymene)] 2-catalyzed one-pot intramolecular and intermolecular carbenoid N-H insertion reactions, respectively, and the prolines are formed with high diastereoselectivities. The catalytic reactions are tolerant toward air/moisture, and the product yields are insensitive to the organic solvents used. © 2008 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/70239
ISSN
1523-7060
2021 Impact Factor: 6.072
2020 SCImago Journal Rankings: 1.940
ISI Accession Number ID
WOS:000254908000007
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorDeng, QHen_HK
dc.contributor.authorXu, HWen_HK
dc.contributor.authorYuen, AWHen_HK
dc.contributor.authorXu, ZJen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:21:01Z-
dc.date.available2010-09-06T06:21:01Z-
dc.date.issued2008en_HK
dc.identifier.citationOrganic Letters, 2008, v. 10 n. 8, p. 1529-1532en_HK
dc.identifier.issn1523-7060en_HK
dc.identifier.urihttp://hdl.handle.net/10722/70239-
dc.description.abstractAryl- and aliphatic-substituted 3-hydroxyprolines and various other amino esters are conveniently prepared by [RuCI2(p-cymene)] 2-catalyzed one-pot intramolecular and intermolecular carbenoid N-H insertion reactions, respectively, and the prolines are formed with high diastereoselectivities. The catalytic reactions are tolerant toward air/moisture, and the product yields are insensitive to the organic solvents used. © 2008 American Chemical Society.en_HK
dc.languageengen_HK
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_HK
dc.relation.ispartofOrganic Lettersen_HK
dc.titleRuthenium-catalyzed one-pot carbenoid N-H insertion reactions and diastereoselective synthesis of prolinesen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1523-7060&volume=10&spage=1529&epage=1532&date=2008&atitle=Ruthenium-Catalyzed+One-Pot+Carbenoid+N-H+Insertion+Reactions+and+Diastereoselective+Synthesis+of+Prolines++en_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol800087pen_HK
dc.identifier.pmid18351765-
dc.identifier.scopuseid_2-s2.0-44449095250en_HK
dc.identifier.hkuros147484en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-44449095250&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume10en_HK
dc.identifier.issue8en_HK
dc.identifier.spage1529en_HK
dc.identifier.epage1532en_HK
dc.identifier.isiWOS:000254908000007-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridDeng, QH=8987982900en_HK
dc.identifier.scopusauthoridXu, HW=7407450997en_HK
dc.identifier.scopusauthoridYuen, AWH=24337152700en_HK
dc.identifier.scopusauthoridXu, ZJ=8708548900en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl1523-7052-

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