A Two-step Asymmetric Synthesis of Pure Trans-(R, R)-Diaryl-epoxides (CROSBI ID 77542)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
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