Enantiopure representatives of the title heterocyclic systems, which are of interest in alkaloid chemistry, are accessible by a procedure based upon intramolecular cycloadditions of nitrones derived from N-(cyclohex-2-enyl)-substituted pyrrole-2- and indole-2-carbaldehyde, followed by reductive manipulation of the cycloadducts.

A valuable approach to enantiopure partially saturated pyrrolo- and indolo[1,2-a]indoles by intramolecular nitrone cycloadditions to the cyclohexene ring / E.M. Beccalli, G. Broggini, A. Farina, L. Malpezzi, A. Terraneo, G. Zecchi. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1434-193X. - :13(2002), pp. 2080-2088.

A valuable approach to enantiopure partially saturated pyrrolo- and indolo[1,2-a]indoles by intramolecular nitrone cycloadditions to the cyclohexene ring

E.M. Beccalli
Primo
;
2002

Abstract

Enantiopure representatives of the title heterocyclic systems, which are of interest in alkaloid chemistry, are accessible by a procedure based upon intramolecular cycloadditions of nitrones derived from N-(cyclohex-2-enyl)-substituted pyrrole-2- and indole-2-carbaldehyde, followed by reductive manipulation of the cycloadducts.
Cycloadditions; Fused-ring systems; Nitrogen heterocycles; Nitrones; Stereoselectivity
Settore CHIM/06 - Chimica Organica
2002
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/199369
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