File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.tetlet.2009.09.175
- Scopus: eid_2-s2.0-70350754541
- WOS: WOS:000271841900029
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Mechanistic investigations of the phosphine-mediated nitrone deoxygenation reaction and its application in cyclic imine synthesis
Title | Mechanistic investigations of the phosphine-mediated nitrone deoxygenation reaction and its application in cyclic imine synthesis |
---|---|
Authors | |
Keywords | Imines Iminosugars Mp2 Calculations Nitrone Deoxygenation Phosphines |
Issue Date | 2009 |
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet |
Citation | Tetrahedron Letters, 2009, v. 50 n. 50, p. 7038-7042 How to Cite? |
Abstract | Carbohydrate-derived cyclic nitrones were deoxygenated to form the corresponding imines using tributylphosphine. Experimental and theoretical investigations by the way of MP2 calculations suggest a revision of the mechanism initially proposed by Kurtzweil and Beak for the triarylphosphine-mediated deoxygenation of nitrones. © 2009 Elsevier Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/168413 |
ISSN | 2023 Impact Factor: 1.5 2023 SCImago Journal Rankings: 0.323 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cividino, P | en_US |
dc.contributor.author | DheuAndries, ML | en_US |
dc.contributor.author | Ou, J | en_US |
dc.contributor.author | Milet, A | en_US |
dc.contributor.author | Py, S | en_US |
dc.contributor.author | Toy, PH | en_US |
dc.date.accessioned | 2012-10-08T03:18:39Z | - |
dc.date.available | 2012-10-08T03:18:39Z | - |
dc.date.issued | 2009 | en_US |
dc.identifier.citation | Tetrahedron Letters, 2009, v. 50 n. 50, p. 7038-7042 | en_US |
dc.identifier.issn | 0040-4039 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168413 | - |
dc.description.abstract | Carbohydrate-derived cyclic nitrones were deoxygenated to form the corresponding imines using tributylphosphine. Experimental and theoretical investigations by the way of MP2 calculations suggest a revision of the mechanism initially proposed by Kurtzweil and Beak for the triarylphosphine-mediated deoxygenation of nitrones. © 2009 Elsevier Ltd. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet | en_US |
dc.relation.ispartof | Tetrahedron Letters | en_US |
dc.subject | Imines | en_US |
dc.subject | Iminosugars | en_US |
dc.subject | Mp2 Calculations | en_US |
dc.subject | Nitrone Deoxygenation | en_US |
dc.subject | Phosphines | en_US |
dc.title | Mechanistic investigations of the phosphine-mediated nitrone deoxygenation reaction and its application in cyclic imine synthesis | en_US |
dc.type | Article | en_US |
dc.identifier.email | Toy, PH:phtoy@hkucc.hku.hk | en_US |
dc.identifier.authority | Toy, PH=rp00791 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2009.09.175 | en_US |
dc.identifier.scopus | eid_2-s2.0-70350754541 | en_US |
dc.identifier.hkuros | 170478 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70350754541&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 50 | en_US |
dc.identifier.issue | 50 | en_US |
dc.identifier.spage | 7038 | en_US |
dc.identifier.epage | 7042 | en_US |
dc.identifier.isi | WOS:000271841900029 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Cividino, P=7801585572 | en_US |
dc.identifier.scopusauthorid | DheuAndries, ML=6504154520 | en_US |
dc.identifier.scopusauthorid | Ou, J=35234687200 | en_US |
dc.identifier.scopusauthorid | Milet, A=6701366879 | en_US |
dc.identifier.scopusauthorid | Py, S=6602523031 | en_US |
dc.identifier.scopusauthorid | Toy, PH=7006579247 | en_US |
dc.identifier.citeulike | 5913446 | - |
dc.identifier.issnl | 0040-4039 | - |