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Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases (CROSBI ID 146025)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Stipetić, Irena ; Roje, Marin ; Hameršak, Zdenko Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases // Synlett, 2008 (2008), 20; 3149-3152. doi: 10.1055/s-0028-1087367

Podaci o odgovornosti

Stipetić, Irena ; Roje, Marin ; Hameršak, Zdenko

engleski

Highly Enantioselective Aziridination of N-Protected Imines : Comparison of the Phosphazene EtP2 and Sodium Hydride as Bases

Asymmetric synthesis of 2, 3-disubstituted N-Boc, N-SES, and N-Ts aziridines starting from N-protected imines, using sulfonium salt derived from Eliel’ s oxathiane, is reported. Sodium hydride was successfully used as a substitute for the phosphazene base EtP2 without any loss of yield, enantioselectivity, or diastereoselectivity.

asymmetric synthesis ; aziridines ; enantioselectivity ; imine ; ylide

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Podaci o izdanju

2008 (20)

2008.

3149-3152

objavljeno

0936-5214

10.1055/s-0028-1087367

Povezanost rada

Kemija

Poveznice
Indeksiranost