A comparative study of the stereoselective addition of trimethylsilyl cyanide and diethylaluminum cyanide to chiral cyclic nitrones-Reference-Cited by-同舟云学术

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A comparative study of the stereoselective addition of trimethylsilyl cyanide and diethylaluminum cyanide to chiral cyclic nitrones

Published:2003-02 Issue:3 Volume:14 Page:367-379
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Merino Pedro,Tejero Tomas,Revuelta Julia,Romero Pilar,Cicchi Stefano,Mannucci Vanni,Brandi Alberto,Goti Andrea

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference59 articles.

1. In this work we use the syn/anti nomenclature according to Masamune convention. See: (a) Masamune, S.; Ali, S. A.; Snitman, D. L.; Garvey, D. S. Angew. Chem., Int. Ed. Engl. 1980, 19, 557–558; (b) Masamune, S.; Kaiho, T.; Garvey, D. S. J. Am. Chem. Soc. 1982, 104, 5521–5523.

2. Diastereoselective Hydrocyanation of Chiral Nitrones. Synthesis of Novel α-(Hydroxyamino) Nitriles

3. For leading references on the synthetic utility of nitrones 2, see: (a) Goti, A.; Cicchi, S.; Cacciarini, M.; Cardona, F.; Fedi, V.; Brandi, A. Eur. J. Org. Chem. 2000, 3633–3645 and references cited therein;

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