Palladium catlyzed reductive cyclization reaction in alkaloid synthesis - an enantioselective total synthetic route to (+)-pumiliotoxin C

DOI: 10.1016/0040-4039(96)00861-1

Source and publish data:

Tetrahedron Letters p. 4401 - 4404 (1996)

Update date:2022-08-03

Topics:

Authors:

Toyota, Masahiro

Asoh, Takanobu

Fukumoto, Keiichiro

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Article abstract of DOI:10.1016/0040-4039(96)00861-1

Beginning with the chirally homogeneous cyclohexenol 3, an enantioselective total synthetic route to (+)-pumiliotoxin C (1) has been described. Palladium catalyzed reductive cyclization reaction was employed to prepare a key component in the synthesis. Co

Full text of DOI:10.1016/0040-4039(96)00861-1

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