Alternative synthesis of (±)-eburunamenine via cleavage of a cyclic dithioacetal of an α-oxo-thione

1 January 1977

journal article
research article
Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications

No. 2,p. 68
https://doi.org/10.1039/c39770000068

Abstract

An alternative synthesis of (±)-eburunamenine (10) is accomplished using the C-9 lactone (5) obtained by cleavage of the cyclic dithioacetal (1) as a building block of the non-tryptamine unit.

Keywords

CLEAVAGE
EBURUNAMENINE
ACCOMPLISHED USING
TRYPTAMINE UNIT
OXO THIONE
BUILDING BLOCK
Α OXO

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