Tetrahedron Letters p. 1059 - 1062 (1980)
Update date:2022-07-29
Topics: Stereochemistry Lactones Bromide Organomagnesium bromide Secologanin tetraacetate Catalytic reduction Pd-C Absolute structures Acetylation Iridoid Benzene ring Mesylation Demesylation Olefin Geometrical isomers Catalytic hydrogenation Epilactone Heptane-1,7-diol Tetrahydropyranyloxyheptanylbromide Benzyloxy
Inouye, Hiroyuki
Takeda, Yoshio
Uesato, Shinichi
Uobe, Kenichi
Hashimoto, Toshiro
Shingu, Tetsuro
Hydrangenoside A, isolated along with its three congeners from Hydrangea macrophylla, was proved to have a novel type of structure which is thought to be biosynthesized through an aldol-type condensation of secologanin with a unit formed by the shikimate-
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(1985)Doi:10.1016/S0040-4039(97)00700-4
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(1985)Doi:10.1080/00397919708003363
(1997)Doi:10.1021/ja00304a043
(1985)