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- Publisher Website: 10.1021/ol901111g
- Scopus: eid_2-s2.0-68149131336
- PMID: 19591453
- WOS: WOS:000268479900036
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Article: Secondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH system
Title | Secondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH system |
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Authors | |
Issue Date | 2009 |
Publisher | American 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? |
Abstract | A 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 Identifier | http://hdl.handle.net/10722/168395 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, OY | en_US |
dc.contributor.author | Law, KL | en_US |
dc.contributor.author | Yang, D | en_US |
dc.date.accessioned | 2012-10-08T03:18:25Z | - |
dc.date.available | 2012-10-08T03:18:25Z | - |
dc.date.issued | 2009 | en_US |
dc.identifier.citation | Organic Letters, 2009, v. 11 n. 15, p. 3302-3305 | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168395 | - |
dc.description.abstract | A 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.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html | en_US |
dc.relation.ispartof | Organic Letters | en_US |
dc.subject.mesh | Aldehydes - Chemistry | en_US |
dc.subject.mesh | Amination | en_US |
dc.subject.mesh | Amines - Chemical Synthesis | en_US |
dc.subject.mesh | Indium - Chemistry | en_US |
dc.subject.mesh | Ketones - Chemistry | en_US |
dc.subject.mesh | Zinc Compounds - Chemistry | en_US |
dc.title | Secondary amine formation from reductive amination of carbonyl compounds promoted by lewis acid using the InCl3ZEt3SiH system | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lee, OY:leeonyi@hku.hk | en_US |
dc.identifier.email | Yang, D:yangdan@hku.hk | en_US |
dc.identifier.authority | Lee, OY=rp00725 | en_US |
dc.identifier.authority | Yang, D=rp00825 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/ol901111g | en_US |
dc.identifier.pmid | 19591453 | - |
dc.identifier.scopus | eid_2-s2.0-68149131336 | en_US |
dc.identifier.hkuros | 180949 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-68149131336&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 11 | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.spage | 3302 | en_US |
dc.identifier.epage | 3305 | en_US |
dc.identifier.isi | WOS:000268479900036 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lee, OY=7103020334 | en_US |
dc.identifier.scopusauthorid | Law, KL=7202563094 | en_US |
dc.identifier.scopusauthorid | Yang, D=7404800756 | en_US |
dc.identifier.issnl | 1523-7052 | - |