Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions
Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis.
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| Formato: | JOUR |
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_14246376_v2002_n10_p14_Brousse |
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todo:paper_14246376_v2002_n10_p14_Brousse2023-10-03T16:13:36Z Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions Brousse, B.N. Moglioni, A.G. Alho, M.M. Álvarez-Larena, Á. Moltrasio, G.Y. D'Accorso, N.B. Asymmetric spiro-heterocyclic compounds Terpenones Thiadiazolines Thiosemicarbazones 1,3,3 trimethyl 2 norcamphanone camphor heterocyclic compound menthone n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide terpene derivative thiadiazoline derivative thiosemicarbazone derivative unclassified drug acetylation article carbohydrate synthesis carbon nuclear magnetic resonance chirality proton nuclear magnetic resonance stereochemistry structure analysis X ray diffraction Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. Fil:Alho, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Moltrasio, G.Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14246376_v2002_n10_p14_Brousse |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Asymmetric spiro-heterocyclic compounds Terpenones Thiadiazolines Thiosemicarbazones 1,3,3 trimethyl 2 norcamphanone camphor heterocyclic compound menthone n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide terpene derivative thiadiazoline derivative thiosemicarbazone derivative unclassified drug acetylation article carbohydrate synthesis carbon nuclear magnetic resonance chirality proton nuclear magnetic resonance stereochemistry structure analysis X ray diffraction |
| spellingShingle |
Asymmetric spiro-heterocyclic compounds Terpenones Thiadiazolines Thiosemicarbazones 1,3,3 trimethyl 2 norcamphanone camphor heterocyclic compound menthone n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide terpene derivative thiadiazoline derivative thiosemicarbazone derivative unclassified drug acetylation article carbohydrate synthesis carbon nuclear magnetic resonance chirality proton nuclear magnetic resonance stereochemistry structure analysis X ray diffraction Brousse, B.N. Moglioni, A.G. Alho, M.M. Álvarez-Larena, Á. Moltrasio, G.Y. D'Accorso, N.B. Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| topic_facet |
Asymmetric spiro-heterocyclic compounds Terpenones Thiadiazolines Thiosemicarbazones 1,3,3 trimethyl 2 norcamphanone camphor heterocyclic compound menthone n [aza(1,7,7 trimethylbicyclo[2.2.1]hept 2 ylidene)methyl]acetamide terpene derivative thiadiazoline derivative thiosemicarbazone derivative unclassified drug acetylation article carbohydrate synthesis carbon nuclear magnetic resonance chirality proton nuclear magnetic resonance stereochemistry structure analysis X ray diffraction |
| description |
Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. |
| format |
JOUR |
| author |
Brousse, B.N. Moglioni, A.G. Alho, M.M. Álvarez-Larena, Á. Moltrasio, G.Y. D'Accorso, N.B. |
| author_facet |
Brousse, B.N. Moglioni, A.G. Alho, M.M. Álvarez-Larena, Á. Moltrasio, G.Y. D'Accorso, N.B. |
| author_sort |
Brousse, B.N. |
| title |
Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| title_short |
Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| title_full |
Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| title_fullStr |
Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| title_full_unstemmed |
Behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| title_sort |
behavior of thiosemicarbazones derived from some terpenones under acetylating conditions |
| url |
http://hdl.handle.net/20.500.12110/paper_14246376_v2002_n10_p14_Brousse |
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AT broussebn behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions AT moglioniag behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions AT alhomm behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions AT alvarezlarenaa behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions AT moltrasiogy behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions AT daccorsonb behaviorofthiosemicarbazonesderivedfromsometerpenonesunderacetylatingconditions |
| _version_ |
1807324311062577152 |