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Article: Secondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH system

TitleSecondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH system
Authors
Issue Date2009
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2009, v. 11 n. 15, p. 3302-3305 How to Cite?
AbstractA robust and reliable method has been developed for reductive amination of primary amines with various aldehydes and ketones using Zn(ClO4) 2.6H20 as a catalyst. [In-H] generated in situ via a combination of InCl3 and Et3SiH is employed as an effective reducing system. A variety of secondary amines can be synthesized in a one-pot procedure in excellent yields. © 2009 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/168395
ISSN
2015 Impact Factor: 6.732
2015 SCImago Journal Rankings: 3.187
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLee, OYen_US
dc.contributor.authorLaw, KLen_US
dc.contributor.authorYang, Den_US
dc.date.accessioned2012-10-08T03:18:25Z-
dc.date.available2012-10-08T03:18:25Z-
dc.date.issued2009en_US
dc.identifier.citationOrganic Letters, 2009, v. 11 n. 15, p. 3302-3305en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10722/168395-
dc.description.abstractA robust and reliable method has been developed for reductive amination of primary amines with various aldehydes and ketones using Zn(ClO4) 2.6H20 as a catalyst. [In-H] generated in situ via a combination of InCl3 and Et3SiH is employed as an effective reducing system. A variety of secondary amines can be synthesized in a one-pot procedure in excellent yields. © 2009 American Chemical Society.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_US
dc.relation.ispartofOrganic Lettersen_US
dc.subject.meshAldehydes - Chemistryen_US
dc.subject.meshAminationen_US
dc.subject.meshAmines - Chemical Synthesisen_US
dc.subject.meshIndium - Chemistryen_US
dc.subject.meshKetones - Chemistryen_US
dc.subject.meshZinc Compounds - Chemistryen_US
dc.titleSecondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH systemen_US
dc.typeArticleen_US
dc.identifier.emailLee, OY:leeonyi@hku.hken_US
dc.identifier.emailYang, D:yangdan@hku.hken_US
dc.identifier.authorityLee, OY=rp00725en_US
dc.identifier.authorityYang, D=rp00825en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/ol901111gen_US
dc.identifier.pmid19591453-
dc.identifier.scopuseid_2-s2.0-68149131336en_US
dc.identifier.hkuros180949-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-68149131336&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume11en_US
dc.identifier.issue15en_US
dc.identifier.spage3302en_US
dc.identifier.epage3305en_US
dc.identifier.isiWOS:000268479900036-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridLee, OY=7103020334en_US
dc.identifier.scopusauthoridLaw, KL=7202563094en_US
dc.identifier.scopusauthoridYang, D=7404800756en_US

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