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Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.provenance | CONICET | - |
dc.creator | Martins Alho, Miriam Amelia | - |
dc.creator | Baggio, Ricardo Fortunato | - |
dc.creator | D'accorso, Norma Beatriz | - |
dc.date | 2015-09-25T15:44:13Z | - |
dc.date | 2015-09-25T15:44:13Z | - |
dc.date | 2013-04-13 | - |
dc.date | 2016-03-30 10:35:44.97925-03 | - |
dc.date.accessioned | 2019-04-29T15:47:42Z | - |
dc.date.available | 2019-04-29T15:47:42Z | - |
dc.date.issued | 2013-04-13 | - |
dc.identifier | Martins Alho, Miriam Amelia; Baggio, Ricardo Fortunato; D'accorso, Norma Beatriz; Cyclization of 1,2:3,4-di-O-isopropylidene-α-D-galacto-1,6-hexodialdo-1,5-pyranose acylhydrazone and semicarbazone; Arkat USA; Arkivoc - Archive for Organic Chemistry; III; 13-4-2013; 129-138 | - |
dc.identifier | 1551-7004 | - |
dc.identifier | http://hdl.handle.net/11336/2130 | - |
dc.identifier | 1551-7012 | - |
dc.identifier.uri | http://rodna.bn.gov.ar:8080/jspui/handle/bnmm/302198 | - |
dc.description | Cyclization of 1,2:3,4-di-O-isopropylidene-α-D-galacto-1,6-hexodialdo-1,5-pyranose benzoylhydrazone using acetylating mixtures led us to the corresponding (2R)- and (2S)-5- phenyl-1,3,4-oxadiazoline derivatives. The same conditions applied to the semicarbazone produced the 5-methyl-1,3,4-oxadiazoline derivative as the main compound, which is formed with acetylating mixtures even at room temperature. X-Ray analysis and NMR techniques were used to determine the stereochemistry of the new asymmetric centers. | - |
dc.description | Fil: Martins Alho, Miriam Amelia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina; Universidad de Buenos Aires. Facultad de Ingeniería. Departamento de Química; Argentina; | - |
dc.description | Fil: Baggio, Ricardo Fortunato. Comisión Nacional de Energía Atómica. Gerencia de Investigación y Aplicaciones; Argentina; | - |
dc.description | Fil: D'accorso, Norma Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina; | - |
dc.format | application/pdf | - |
dc.format | application/pdf | - |
dc.language | eng | - |
dc.publisher | Arkat USA | - |
dc.relation | info:eu-repo/semantics/altIdentifier/url/http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/2013/3/ | - |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.3998/ark.5550190.0014.311 | - |
dc.relation | info:eu-repo/semantics/altIdentifier/url/http://quod.lib.umich.edu/a/ark/5550190.0014.311/2/--cyclization-of-1234-di-o-isopropylidene-%CE%B1-d-galacto-16?page=root;size=150;view=text | - |
dc.rights | info:eu-repo/semantics/openAccess | - |
dc.rights | https://creativecommons.org/licenses/by-nc/2.5/ar/ | - |
dc.source | reponame:CONICET Digital (CONICET) | - |
dc.source | instname:Consejo Nacional de Investigaciones Científicas y Técnicas | - |
dc.source | instacron:CONICET | - |
dc.source.uri | http://hdl.handle.net/11336/2130 | - |
dc.subject | OXADIAZOLINES | - |
dc.subject | SUGAR HETEROCYCLES | - |
dc.subject | SEMICARBAZONES | - |
dc.subject | ACETYLATION | - |
dc.subject | Química Orgánica | - |
dc.subject | Ciencias Químicas | - |
dc.subject | CIENCIAS NATURALES Y EXACTAS | - |
dc.title | Cyclization of 1,2:3,4-di-O-isopropylidene-α-D-galacto-1,6-hexodialdo-1,5-pyranose acylhydrazone and semicarbazone | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.type | info:ar-repo/semantics/articulo | - |
Aparece en las colecciones: | CONICET |
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