On stereochemistry of osmium tetroxide oxidation of allylic alcohol systems: examples
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[1] W. Christ,et al. Stereochemistry of palytoxin. Part 3. C7-C51 segment , 1982 .
[2] J. M. Finan,et al. Stereochemistry of palytoxin. Part 2. C1-C6, C47-C74, and C77-C83 segments , 1982 .
[3] V. Martín,et al. Synthesis of saccharides and related polyhydroxylated natural products. 2. Simple deoxyalditols , 1982 .
[4] J. Secrist,et al. Synthesis of methyl peracetyl .alpha.-hikosaminide, the undecose portion of the nucleoside antibiotic hikizimycin , 1980 .
[5] M. Schroeder. Osmium tetraoxide cis hydroxylation of unsaturated substrates , 1980 .
[6] D. Vyas,et al. Studies on the Synthesis of Novel Carbohydrates with Sulfur in the Ring. Part III. The Synthesis of Derivatives of 2,6-Dithio-hex-4-en-2-ulopyranosidononitriles , 1975 .
[7] R. Srivastava,et al. Total Synthesis of 4-O-Methyl-DL-lyxose and 4-Deoxy-DL-ribose. Further Evidence of the Stereoselective Hydroxylation of Double Bonds by Osmic Acid , 1971 .
[8] N. K. Kochetkov,et al. New route to higher sugars , 1965 .
[9] T. Posternak,et al. Recherches dans la série des cyclitols XVI. Sur quelques cyclohexane‐tétrols‐1,2,3,4 , 1953 .