Events The 1st International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

10.3390/ecsoc-1-02011

This submission belongs to the session a. General Organic Synthesis of the event The 1st International Electronic Conference on Synthetic Organic Chemistry

Published date

01 Sep, 1997

Citation

Andrea Goti, Alberto Brandi, Valentina Fedi, A Straightforward Route to Enantiopure Pyrrolizidines by Cycloaddition to Pyrroline N-Oxides Derived from the Chiral Pool, in Proceedings of The 1st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1997, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-1-02011

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A Straightforward Route to Enantiopure Pyrrolizidines by Cycloaddition to Pyrroline N-Oxides Derived from the Chiral Pool

Valentina Fedi ¹

Alberto Brandi ¹

Andrea Goti ¹

1. Centro di Studio C.N.R. sulla Chimica e la Struttura dei Composti Eterociclici e loro Applicazioni (CSCEA), Dipartimento di Chimica organica "Ugo Schiff", Universita di Firenze, via G. Capponi 9, I-50121 Firenze, Italy.

Abstract

We have recently reported the synthesis of enantiopure 3-heterosubstituted pyrroline N-oxides of type 1 and 2 (Scheme 1) obtained by oxidation of the corresponding hydroxylamines, in turn available in large amounts from L-malic and L-aspartic acids, respectively.1

Keywords

n/a

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