Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds

Lithium iodide proves to be a very efficient catalyst for Michael addition of β-dicarbonyl compounds. The successful application of this methodology to α,β-unsaturated aldehdes allows an improved approach to 5,6-disubstituted cyclohex-2-en-1-ones. © 1991.

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Detalles Bibliográficos
Autores principales:	Antonioletti, R., Bonadies, F., Monteagudo, E.S., Scettri, A.
Formato:	JOUR
Materias:	carboxylic acid derivative cyclohexane derivative ketone article priority journal reaction analysis synthesis
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_00404039_v32_n39_p5373_Antonioletti
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

id	todo:paper_00404039_v32_n39_p5373_Antonioletti
record_format	dspace
spelling	todo:paper_00404039_v32_n39_p5373_Antonioletti2023-10-03T14:50:47Z Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds Antonioletti, R. Bonadies, F. Monteagudo, E.S. Scettri, A. carboxylic acid derivative cyclohexane derivative ketone article priority journal reaction analysis synthesis Lithium iodide proves to be a very efficient catalyst for Michael addition of β-dicarbonyl compounds. The successful application of this methodology to α,β-unsaturated aldehdes allows an improved approach to 5,6-disubstituted cyclohex-2-en-1-ones. © 1991. Fil:Monteagudo, E.S. 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_00404039_v32_n39_p5373_Antonioletti
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-134
collection	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic	carboxylic acid derivative cyclohexane derivative ketone article priority journal reaction analysis synthesis
spellingShingle	carboxylic acid derivative cyclohexane derivative ketone article priority journal reaction analysis synthesis Antonioletti, R. Bonadies, F. Monteagudo, E.S. Scettri, A. Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
topic_facet	carboxylic acid derivative cyclohexane derivative ketone article priority journal reaction analysis synthesis
description	Lithium iodide proves to be a very efficient catalyst for Michael addition of β-dicarbonyl compounds. The successful application of this methodology to α,β-unsaturated aldehdes allows an improved approach to 5,6-disubstituted cyclohex-2-en-1-ones. © 1991.
format	JOUR
author	Antonioletti, R. Bonadies, F. Monteagudo, E.S. Scettri, A.
author_facet	Antonioletti, R. Bonadies, F. Monteagudo, E.S. Scettri, A.
author_sort	Antonioletti, R.
title	Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
title_short	Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
title_full	Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
title_fullStr	Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
title_full_unstemmed	Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
title_sort	lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds
url	http://hdl.handle.net/20.500.12110/paper_00404039_v32_n39_p5373_Antonioletti
work_keys_str_mv	AT antoniolettir lithiumiodidecatalyzedconjugateadditionofbdicarbonylcompounds AT bonadiesf lithiumiodidecatalyzedconjugateadditionofbdicarbonylcompounds AT monteagudoes lithiumiodidecatalyzedconjugateadditionofbdicarbonylcompounds AT scettria lithiumiodidecatalyzedconjugateadditionofbdicarbonylcompounds
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Lithium iodide-catalyzed conjugate addition of β-dicarbonyl compounds

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