AN EFFICIENT AND HIGHLY REGIOSELECTIVE INTRAMOLECULAR MANNICH-TYPE REACTION: A CONSTRUCTION OF THE AEF RING SYSTEM OF ACONITINE-TYPE DITERPENE ALKALOIDS

DOI: 10.1016/S0040-4039(00)84207-0

Source and publish data:

Tetrahedron Letters p. 1167 - 1170 (1986)

Update date:2022-08-02

Topics:

Authors:

Shishido, Kozo

Hiroya, Kou

Fukumoto, Keiichiro

Kametani, Tetsuji

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Article abstract of DOI:10.1016/S0040-4039(00)84207-0

An efficient and highly regioselective intramolecular Mannich-type reaction has been developed.The utility of the methodology, combined with a stereoselective intramolecular Diels-Alder reaction, for the construction of the AEF ring system of aconitine-type alkaloids has been exemplified.

Full text of DOI:10.1016/S0040-4039(00)84207-0

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