Tetrahedron Letters p. 4979 - 4982 (1998)
Update date:2022-08-02
Topics:
Dankwardt, John W.
Dankwardt, Sharon M.
Schlessinger, Richard H.
The synthesis of the C-19 through C-27 segment of the marine natural product okadaic acid was accomplished employing a highly enantio- and diasteroselective aldol coupling reaction of a chiral vinylogous urethane lactone enolate. The remainder of the carb
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Doi:10.1016/S0960-894X(98)00315-1
(1998)Doi:10.1039/c9dt04062e
(2020)Doi:10.1007/BF02501360
()Doi:10.1016/S0040-4039(98)01183-6
(1998)Doi:10.1016/S0040-4039(98)01372-0
(1998)Doi:10.1039/c6ob01394e
(2016)
