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- Publisher Website: 10.1021/jo049174f
- Scopus: eid_2-s2.0-6444239844
- PMID: 15497984
- WOS: WOS:000224707900022
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Article: Synthesis of chiral β3-aminoxy peptides
Title | Synthesis of chiral β3-aminoxy peptides |
---|---|
Authors | |
Issue Date | 2004 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc |
Citation | Journal Of Organic Chemistry, 2004, v. 69 n. 22, p. 7577-7581 How to Cite? |
Abstract | A series of chiral β3-aminoxy acids or amides with various side chains have been synthesized via two different approaches. One is the Arndt-Eistert homologation approach, using chiral α-aminoxy acids as starting materials. The other approach, utilizing the enantioselective reduction of β-keto esters catalyzed by baker's yeast or chiral Ru(II) complexes, produces chiral β3-aminoxy acids with nonproteinaceous side chains. The oligomers of β3-aminoxy acids can be readily prepared using EDCI/HOAt as the coupling reagent. |
Persistent Identifier | http://hdl.handle.net/10722/168370 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 0.724 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, D | en_US |
dc.contributor.author | Zhang, YH | en_US |
dc.contributor.author | Li, B | en_US |
dc.contributor.author | Zhang, DW | en_US |
dc.date.accessioned | 2012-10-08T03:18:04Z | - |
dc.date.available | 2012-10-08T03:18:04Z | - |
dc.date.issued | 2004 | en_US |
dc.identifier.citation | Journal Of Organic Chemistry, 2004, v. 69 n. 22, p. 7577-7581 | en_US |
dc.identifier.issn | 0022-3263 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168370 | - |
dc.description.abstract | A series of chiral β3-aminoxy acids or amides with various side chains have been synthesized via two different approaches. One is the Arndt-Eistert homologation approach, using chiral α-aminoxy acids as starting materials. The other approach, utilizing the enantioselective reduction of β-keto esters catalyzed by baker's yeast or chiral Ru(II) complexes, produces chiral β3-aminoxy acids with nonproteinaceous side chains. The oligomers of β3-aminoxy acids can be readily prepared using EDCI/HOAt as the coupling reagent. | en_US |
dc.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc | en_US |
dc.relation.ispartof | Journal of Organic Chemistry | en_US |
dc.subject.mesh | Amides - Chemical Synthesis | en_US |
dc.subject.mesh | Amino Acids - Chemical Synthesis | en_US |
dc.subject.mesh | Catalysis | en_US |
dc.subject.mesh | Molecular Structure | en_US |
dc.subject.mesh | Nuclear Magnetic Resonance, Biomolecular | en_US |
dc.subject.mesh | Peptides - Chemical Synthesis | en_US |
dc.subject.mesh | Stereoisomerism | en_US |
dc.title | Synthesis of chiral β3-aminoxy peptides | en_US |
dc.type | Article | en_US |
dc.identifier.email | Yang, D:yangdan@hku.hk | en_US |
dc.identifier.authority | Yang, D=rp00825 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/jo049174f | en_US |
dc.identifier.pmid | 15497984 | - |
dc.identifier.scopus | eid_2-s2.0-6444239844 | en_US |
dc.identifier.hkuros | 102005 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-6444239844&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 69 | en_US |
dc.identifier.issue | 22 | en_US |
dc.identifier.spage | 7577 | en_US |
dc.identifier.epage | 7581 | en_US |
dc.identifier.isi | WOS:000224707900022 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Yang, D=7404800756 | en_US |
dc.identifier.scopusauthorid | Zhang, YH=8379010100 | en_US |
dc.identifier.scopusauthorid | Li, B=36072052100 | en_US |
dc.identifier.scopusauthorid | Zhang, DW=35320759400 | en_US |
dc.identifier.issnl | 0022-3263 | - |