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Article: Silver(i)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions

TitleSilver(i)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions
Authors
KeywordsOrganic chemistry
Issue Date2010
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
Citation
Chemical Communications, 2010, v. 46 n. 2, p. 213-215 How to Cite?
AbstractSilver(i) salts mediated stereospecific transformation of optically active propargylamines to axially chiral allenes with excellent enantioselectivities (17 examples with 96-99% ee; one substrate with 91% ee) without subsequent racemization. © 2010 The Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/144849
ISSN
2015 Impact Factor: 6.567
2015 SCImago Journal Rankings: 2.771
ISI Accession Number ID
Funding AgencyGrant Number
The University of Hong Kong (University Development Fund)
Hong Kong Research Grant Council (HKU)7052/07P
University Grants Committee of the Hong Kong Special Administrative Region, ChinaAoE/P-10/01
Funding Information:

We are grateful for the financial support of The University of Hong Kong (University Development Fund), Hong Kong Research Grant Council (HKU 7052/07P), and the Areas of Excellence Scheme established under the University Grants Committee of the Hong Kong Special Administrative Region, China (AoE/P-10/01).

References
Grants

 

DC FieldValueLanguage
dc.contributor.authorLo, VKYen_HK
dc.contributor.authorZhou, CYen_HK
dc.contributor.authorWong, MKen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2012-02-14T04:34:49Z-
dc.date.available2012-02-14T04:34:49Z-
dc.date.issued2010en_HK
dc.identifier.citationChemical Communications, 2010, v. 46 n. 2, p. 213-215en_HK
dc.identifier.issn1359-7345en_HK
dc.identifier.urihttp://hdl.handle.net/10722/144849-
dc.description.abstractSilver(i) salts mediated stereospecific transformation of optically active propargylamines to axially chiral allenes with excellent enantioselectivities (17 examples with 96-99% ee; one substrate with 91% ee) without subsequent racemization. © 2010 The Royal Society of Chemistry.en_HK
dc.languageeng-
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.aspen_HK
dc.relation.ispartofChemical Communicationsen_HK
dc.subjectOrganic chemistry-
dc.titleSilver(i)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditionsen_HK
dc.typeArticleen_HK
dc.identifier.emailZhou, CY:cyzhou@hku.hken_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityZhou, CY=rp00843en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b914516hen_HK
dc.identifier.pmid20024329-
dc.identifier.scopuseid_2-s2.0-75649145831en_HK
dc.identifier.hkuros172480-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-75649145831&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume46en_HK
dc.identifier.issue2en_HK
dc.identifier.spage213en_HK
dc.identifier.epage215en_HK
dc.identifier.isiWOS:000272799200003-
dc.publisher.placeUnited Kingdomen_HK
dc.relation.projectInstitute of molecular technology for drug discovery and synthesis-
dc.identifier.scopusauthoridLo, VKY=13406071200en_HK
dc.identifier.scopusauthoridZhou, CY=35742480200en_HK
dc.identifier.scopusauthoridWong, MK=7403908449en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK

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