English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/17597
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

DC FieldValueLanguage
dc.contributor.authorFrancisco, Cosme G.en_US
dc.contributor.authorFreire, Raimundoen_US
dc.contributor.authorHernández, Rosendoen_US
dc.contributor.authorMelián, Danielen_US
dc.contributor.authorSalazar, José A.en_US
dc.contributor.authorSuárez, Ernestoen_US
dc.date.accessioned2009-10-09T09:39:11Z-
dc.date.available2009-10-09T09:39:11Z-
dc.date.issued1984en_US
dc.identifier.citationJournal of the Chemical Society - Perkin Transactions 1984: 459-465 (1984)en_US
dc.identifier.issn1472-7781-
dc.identifier.urihttp://hdl.handle.net/10261/17597-
dc.description7 pages, 3 tables, 3 schemes.-
dc.description.abstractThe reaction of (-)-α-pinene (1) with sodium nitrite-acetic acid gave principally (2S,2R)-2-nitromentha-1(6),8-diene (2) and smaller amounts of (2S,4R)-2-nitromenth-1(6)-en-8-yl acetate (3), (1R,4S)-2-endo-nitrato-6-endo-nitrobornane (4), (1S,4R)-3,3-dimethyl-2-endo-nitrato-6-exo-nitro-8,9-dinorbornane (5), and (-)-3-nitropin-2-3n3 (6). A similar reaction with (-)-β-pinene (8) afforded (4S)-7-nitromentha-1,8-diene (9) as the major product and (4S)-7-nitromenth-1-en-8-yl acetate (10), (1S,4S)-2-endo-nitrato-10-nitrobornane (11), and (1R,4S)-3,3-dimethyl-2-endo-nitrato-10-nitro-8,9-dinorbornane (12) in lower yields. Treatment of the nitro-nitrates (11) and (12) in basic medium gave the corresponding 10,10-dinitro alcohols (20) and (21) by intramo,ecular transfer of the nitro group with retention of configuration at C-2. In stronger alkaline conditions the dinitro endo-alcohol (21) produced unexpectedly the epimeric exo-alcohol (22). The neighbouring participation of the 10,10-dinitro group is shown to be essential for the epimerization to take place. Plausible mechanisms for these reactions are proposed.-
dc.description.sponsorshipPart of this work was supported by the Investigation Programme of the Comisión Asesora de Investigación Científica y Técnica.-
dc.format.extent2373 bytes-
dc.format.extent1180043 bytes-
dc.format.mimetypetext/plain-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistry (UK)-
dc.rightsclosedAccessen_US
dc.titleThe action of sodium nitrite–acetic acid on α- and β-pinene. Participation by a neighbouring geminal dinitro group in the base-catalysed epimerization of a secondary alcoholen_US
dc.typeartículoen_US
dc.identifier.doi10.1039/P19840000459-
dc.relation.publisherversionhttp://dx.doi.org/10.1039/P19840000459-
dc.contributor.funderComisión Asesora de Investigación Científica y Técnica, CAICYT (España)-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100007272es_ES
Appears in Collections:(IPNA) Artículos
Files in This Item:
There are no files associated with this item.
Show simple item record
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.