A vinylogous urethane approach towards the synthesis of okadaic acid. Construction of the C9-C18 fragment. Part II

DOI: 10.1016/S0040-4039(98)00972-1

Source and publish data:

Tetrahedron Letters p. 4975 - 4978 (1998)

Update date:2022-07-30

Topics:

Authors:

Dankwardt M, Sharon

Dankwardt, John W.

Schlessinger, Richard H.

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Article abstract of DOI:10.1016/S0040-4039(98)00972-1

A diastereo- and enantioselective acylation-reduction sequence of a vinylogous urethane lactone silylketene acetal sets the initial stereocenter in this approach towards the C9-C18 fragment of okadaic acid. The remainder of the stereocenters are installed

Full text of DOI:10.1016/S0040-4039(98)00972-1

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