
Tetrahedron Letters p. 1059 - 1062 (1980)
Update date:2022-07-29
Topics: Stereochemistry Lactones Bromide Catalytic reduction Pd-C Acetylation Iridoid Benzene ring Demesylation Olefin Geometrical isomers Catalytic hydrogenation 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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Doi:10.1002/anie.202011140
(2021)Doi:10.1021/jo00218a020
(1985)Doi:10.1016/S0040-4039(97)00700-4
(1997)Doi:10.1021/jo00220a023
(1985)Doi:10.1080/00397919708003363
(1997)Doi:10.1021/ja00304a043
(1985)