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A Two-step Asymmetric Synthesis of Pure Trans-(R, R)-Diaryl-epoxides (CROSBI ID 77542)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Solladie-Cavallo, Arlette ; Diep-Vohuule, Anh ; Šunjić, Vitomir ; Vinković, Vladimir A Two-step Asymmetric Synthesis of Pure Trans-(R, R)-Diaryl-epoxides // Tetrahedron: asymmetry, 7 (1996), 6; 1783-1787. doi: 10.1016/0957-4166(96)00213-3

Podaci o odgovornosti

Solladie-Cavallo, Arlette ; Diep-Vohuule, Anh ; Šunjić, Vitomir ; Vinković, Vladimir

engleski

A Two-step Asymmetric Synthesis of Pure Trans-(R, R)-Diaryl-epoxides

Pure trans-(R, R)-diaryl-epoxides are obtained in two steps and under aprotic conditions using Eliel's oxathiane as the chiral auxiliary. The enantiomeric excesses, determined by chiral HPLC, are 97.9% to 99.9% and the oxathiane is recovered in 78% to 92% yield and may thus be re-used.

Optically-active epoxides ; Halostachine analog ; Stilbene oxides ; Sulfur ; Ylides

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Podaci o izdanju

7 (6)

1996.

1783-1787

objavljeno

0957-4166

1362-511X

10.1016/0957-4166(96)00213-3

Povezanost rada

Kemija

Poveznice
Indeksiranost