Asymmetric and doubly asymmetric 1,3-dipolar cycloadditons in the synthesis of enantiopure organophosphorus compounds

Article abstract of DOI:10.1080/10426509908546263

Enantiopure five-membered ring nitrones derived from L-tartaric acid and from L-malic acid undergo highly regio- and stereoselective cycloaddition reactions with an excess of racemic 2,3-dihydro-1-phenyl-1H-phospholes producing two readily separable tricy

Full text of DOI:10.1080/10426509908546263

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Phosphorus, Sulfur, and
Silicon and the Related
Elements
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Asymmetric and Doubly
Asymmetric 1,3-Dipolar
Cycloadditons in the
Synthesis of Enantiopure
Organophosphorus
Compounds
K. Michaz Pietrusiewicz , Wieszawa
Hozody , Marek Koprowski , Stefano
Cicchi , Andrea Goti & Alberto Brandi
a
Department of Organic Chemistry , M.
Curie-Sklodowska University , Gliniana
3
3, 20-031 Lublin, Poland
b
Department of Organic Chemistry , M.
Curie-Sklodowska University , Gliniana
3
3, 20-031 Lublin, Poland
c
Centre of Molecular and
Macromolecular Studies, P.A.S ,
Sienkiewicza 112, Lódź, Poland
d
Dipartimento di Chimica Organica ,
Universita di Firenze , via Capponi 9,
50121 Firenze, Italy

e
Dipartimento di Chimica Organica ,
Universita di Firenze , via Capponi 9,
5
0121 Firenze, Italy
f
Dipartimento di Chimica Organica ,
Universita di Firenze , via Capponi 9,
0121 Firenze, Italy
5
Published online: 17 Mar 2008.
To cite this article: K. Michaz Pietrusiewicz , Wieszawa Hozody ,
Marek Koprowski , Stefano Cicchi , Andrea Goti & Alberto Brandi (1999)
Asymmetric and Doubly Asymmetric 1,3-Dipolar Cycloadditons in the
Synthesis of Enantiopure Organophosphorus Compounds, Phosphorus,
Sulfur, and Silicon and the Related Elements, 144:1, 389-392, DOI:
10.1080/10426509908546263
To link to this article: http://dx.doi.org/10.1080/10426509908546263
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