Tetrahedron Letters p. 6925 - 6928 (1993)
Update date:2022-08-04
Topics:
Vidari, Giovanni
Giori, Andrea
Dapiaggi, Antonella
Lanfranchi, Gianluigi
The asymmetric Sharpless' dihydroxylation of linalool, citronellyl acetate and nerolidol was investigated. High diastereo-, enantio- and positional selectivity was observed for the first two terpenes. A highly diastereo- and enantioselective synthesis of (3S,6S)-tetrahydro- 2,2,6-trimethyl-6-vinyl-2H-pyran-3-ol is described.
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Doi:10.2478/s11532-013-0233-4
(2013)Doi:10.1002/ardp.19933261013
(1993)Doi:10.1021/ja4025116
(2013)Doi:10.1246/bcsj.66.3128
(1993)Doi:10.1002/anie.201911465
(2020)Doi:10.1039/c3cc46132g
(2014)
