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, Enrique Luis, Sánchez, Eduardo Luis
Publicado:	1983
Materias:	Acoranes Polyphosphoric Acid Spirocyclisation
Acceso en línea:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v38_n4_p497_Michelotti 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	paper:paper_09320776_v38_n4_p497_Michelotti
record_format	dspace
spelling	paper:paper_09320776_v38_n4_p497_Michelotti2023-06-08T15:53:03Z Stereospecific Synthesis of 4,8-Dimethylspiro(4, 5)-deca-7-ene-1,6-dione a Synthetic Route to the Acoranes Michelotti, Enrique Luis Sánchez, Eduardo Luis 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. 1983 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v38_n4_p497_Michelotti 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, Enrique Luis Sánchez, Eduardo Luis 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.
author	Michelotti, Enrique Luis Sánchez, Eduardo Luis
author_facet	Michelotti, Enrique Luis Sánchez, Eduardo Luis
author_sort	Michelotti, Enrique Luis
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
publishDate	1983
url	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v38_n4_p497_Michelotti http://hdl.handle.net/20.500.12110/paper_09320776_v38_n4_p497_Michelotti
work_keys_str_mv	AT michelottienriqueluis stereospecificsynthesisof48dimethylspiro45deca7ene16dioneasyntheticroutetotheacoranes AT sanchezeduardoluis stereospecificsynthesisof48dimethylspiro45deca7ene16dioneasyntheticroutetotheacoranes
_version_	1768543091875119104

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

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