Journal of Organic Chemistry p. 3886 - 3888 (1988)
Update date:2022-08-02
Topics:
Hori, Keiko
Ohfune, Yasufumi
The structure of galantinamic acid (2) has been confirmed to be (2R,3S,5S,6R)-25 by the stereoselective synthesis of each of the eight diastereomers derived from L-lysine; total synthesis of the natural form was accomplished by starting from D-lysine
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Doi:10.1016/S0040-4039(00)96331-7
(1987)Doi:10.1016/S0040-4039(00)96294-4
(1987)Doi:10.1021/om800840u
(2009)Doi:10.1021/ja403523p
(2013)Doi:10.1007/s10593-008-0064-y
(2008)Doi:10.1021/jo00243a027
(1988)
