Stereospecific synthesis and absolute configuration of (+)-rhododendrol
1993
Das, B. | Rao, S.P. | Srinivas, K.V.N.S. | Yadav, J.S.
The stereospecific synthesis of (+)-rhododendrol, a constituent of Rhododendron maximum and Acer nikoense, by enzymatic reduction of 4-(4'-hydroxyphenyl)-2-butanone has shown that the absolute configuration of the molecule is S.
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Bibliographic information
Publisher
American Dairy Science Association
Other Subjects
Molecular conformation; Chemical constituents of plants; Acer nikoense; Rhododendron maximum; Stereochemistry
Language
English
Note
2019-12-05
Type
Journal Article; Text
2024-02-28
MODS
Data Provider
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