
Journal of Organic Chemistry p. 1378 - 1380 (1982)
Update date:2022-08-05
Topics:
Ma, P.
Martin, V. S.
Masamune, S.
Sharpless, K. B.
Viti, S. M.
Asymmetric epoxidation of allylic alcohols followed by selective hydride reduction provides a new route to chiral 1,3-diols and 1,3,5-triols; one of the 1,3,5-triols (21) is also synthesized from D-glucose.
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Doi:10.1021/ja01201a520
(1947)Doi:10.1021/om050594k
(2005)Doi:10.1039/jr9340000052
(1934)Doi:10.1021/jm5005489
(2014)Doi:10.1016/S0040-4020(01)91924-6
(1983)Doi:10.1021/ja00363a023
(1983)