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. BeccalliPrimo
;
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.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.