Related Experiment Videos
Stereoselective approach to hydroxyindolizidines: protection/deprotection of the nitrone functionality via
F M Cordero1, M Gensini, A Goti
1Dipartimento di Chimica Organica "U. Schiff", Centro di Studio sulla Chimica e la Struttura dei Composti Eterociclici e loro Applicazioni - C.N.R., Università di Firenze, via G. Capponi 9, I-50121 Firenze, Italy. cordero@chimorg.unifi.it
Abstract:
The enantiomerically pure indolizidine (-)-21 has been synthesized starting from L-malic acid. The key intermediate 20 has been assembled through an intramolecular 1,3-dipolar cycloaddition of a nitrone generated in situ by retrocycloaddition from isoxazolidine 17 or 18. The configuration of the new three stereocenters was set up with complete control in the cycloaddition step. The presented synthetic route provides a general and highly selective methodology toward indolizidines having the [1,8a]-cis configuration.