Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes

A stereospecific synthesis of 4,8-dimethylspiro(4,5)-deca-7-ene-1,6-dione from 4,7-dimethylcoumarine in high yield is reported. The configuration of this product is established according to its 1 H NMR and 13 C NMR data. © 1983, Walter de Gruyter. All rights reserved.

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Detalles Bibliográficos
Autores principales: Michelotti, E.L., Sanchez+, E.L.
Formato: JOUR
Materias:
Acoranes
Polyphosphoric Acid
Spirocyclisation
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_09320776_v38_n4_p497_Michelotti
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id todo:paper_09320776_v38_n4_p497_Michelotti
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spelling todo:paper_09320776_v38_n4_p497_Michelotti2023-10-03T15:48:22Z Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes Michelotti, E.L. Sanchez+, E.L. Acoranes Polyphosphoric Acid Spirocyclisation A stereospecific synthesis of 4,8-dimethylspiro(4,5)-deca-7-ene-1,6-dione from 4,7-dimethylcoumarine in high yield is reported. The configuration of this product is established according to its 1 H NMR and 13 C NMR data. © 1983, Walter de Gruyter. All rights reserved. Fil:Michelotti, E.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sanchez+, E.L. 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_09320776_v38_n4_p497_Michelotti
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Acoranes
Polyphosphoric Acid
Spirocyclisation
spellingShingle Acoranes
Polyphosphoric Acid
Spirocyclisation
Michelotti, E.L.
Sanchez+, E.L.
Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
topic_facet Acoranes
Polyphosphoric Acid
Spirocyclisation
description A stereospecific synthesis of 4,8-dimethylspiro(4,5)-deca-7-ene-1,6-dione from 4,7-dimethylcoumarine in high yield is reported. The configuration of this product is established according to its 1 H NMR and 13 C NMR data. © 1983, Walter de Gruyter. All rights reserved.
format JOUR
author Michelotti, E.L.
Sanchez+, E.L.
author_facet Michelotti, E.L.
Sanchez+, E.L.
author_sort Michelotti, E.L.
title Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
title_short Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
title_full Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
title_fullStr Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
title_full_unstemmed Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes
title_sort stereospecific synthesis of 4,8-dimethylspiro(4, 5)-deca-7-ene-1,6-dione a synthetic route to the acoranes
url http://hdl.handle.net/20.500.12110/paper_09320776_v38_n4_p497_Michelotti
work_keys_str_mv AT michelottiel stereospecificsynthesisof48dimethylspiro45deca7ene16dioneasyntheticroutetotheacoranes
AT sanchezel stereospecificsynthesisof48dimethylspiro45deca7ene16dioneasyntheticroutetotheacoranes
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