Totalsynthese von natülichem α-Tocopherol. 5. Mitteilung. Asymmetrische Alkylierung und asymmetrische Epoxidierung als Methoden zur Einführung der (R)-Konfiguration an C(2) des Chroman-Systems
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference45 articles.
1. Totalsynthese von nat�rlichem ?-Tocopherol. 4. Mitteilung. Aufbau des Chromanringsystems aus Trimethylhydrochinon und einem optisch aktiven C4- bzw. C5-Synthon
2. A novel total synthesis of (2R,4'R,8'R)-.alpha.-tocopherol (vitamin E). Construction of chiral chromans from an optically active, nonaromatic precursor
3. Totalsynthese von nat�rlichem ?-Tocopherol. 2. Mitteilung. Aufbau der Seitenkette aus (?)-(S)-3-Methyl-?-butyrolacton
4. Über die Chemie des Vitamins E 7. Mitteilung [1] die stereospezifische Cyclisierung von (3′R, 7′R, 11′R)-α-Tocopherolchinon
5. Studies on the total synthesis of (2R, 4'R, 8'R)-.alpha.-tocopherol (vitamin E). Stereospecific cyclizations leading to optically active chromans
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