Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II

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Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural α,β-unsaturated and bicyclic terpenones is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. ©ARKAT.

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Detalles Bibliográficos
Autores principales: Rouge, P.D., Brousse, B.N., Moglioni, A.G., Cozzi, G.A., Alvarez-Larena, A., D'Accorso, N., Moltrasio, G.Y.
Formato: Artículo publishedVersion
Lenguaje:Inglés
Publicado: 2005
Materias:
Spiro-nitrogenheterocycles
Spiro-sulphur heterocycles
Terpenoids
Thiadiazolines
Thiosemicarbazones
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p8_Rouge
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paperaa:paper_14246376_v2005_n12_p8_Rouge
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spelling paperaa:paper_14246376_v2005_n12_p8_Rouge2023-06-12T16:50:12Z Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II Arkivoc 2005;2005(12):8-21 Rouge, P.D. Brousse, B.N. Moglioni, A.G. Cozzi, G.A. Alvarez-Larena, A. D'Accorso, N. Moltrasio, G.Y. Spiro-nitrogenheterocycles Spiro-sulphur heterocycles Terpenoids Thiadiazolines Thiosemicarbazones Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural α,β-unsaturated and bicyclic terpenones is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. ©ARKAT. Fil:D'Accorso, N. 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. 2005 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p8_Rouge
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language Inglés
orig_language_str_mv eng
topic Spiro-nitrogenheterocycles
Spiro-sulphur heterocycles
Terpenoids
Thiadiazolines
Thiosemicarbazones
spellingShingle Spiro-nitrogenheterocycles
Spiro-sulphur heterocycles
Terpenoids
Thiadiazolines
Thiosemicarbazones
Rouge, P.D.
Brousse, B.N.
Moglioni, A.G.
Cozzi, G.A.
Alvarez-Larena, A.
D'Accorso, N.
Moltrasio, G.Y.
Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
topic_facet Spiro-nitrogenheterocycles
Spiro-sulphur heterocycles
Terpenoids
Thiadiazolines
Thiosemicarbazones
description Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural α,β-unsaturated and bicyclic terpenones is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. ©ARKAT.
format Artículo
Artículo
publishedVersion
author Rouge, P.D.
Brousse, B.N.
Moglioni, A.G.
Cozzi, G.A.
Alvarez-Larena, A.
D'Accorso, N.
Moltrasio, G.Y.
author_facet Rouge, P.D.
Brousse, B.N.
Moglioni, A.G.
Cozzi, G.A.
Alvarez-Larena, A.
D'Accorso, N.
Moltrasio, G.Y.
author_sort Rouge, P.D.
title Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
title_short Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
title_full Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
title_fullStr Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
title_full_unstemmed Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II
title_sort behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. part ii
publishDate 2005
url http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p8_Rouge
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