Enantioselective Separation of 4,8-DHT and Phytotoxicity of the Enantiomers on Various Plant Species

Enantioselective Separation of 4,8-DHT and Phytotoxicity of the Enantiomers on Various Plant Species

As a candidate for bioherbicide, 4,8-dihydroxy-1-tetralone (4,8-DHT) was isolated from Caryospora callicarpa epicarp and its two enantiomers, S-(+)-isosclerone and R-(−)-regiolone, were separated by chiral high-performance liquid chromatography (HPLC) on a Chiralcel OD column with chiral stationary...

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Bibliographic Details
Main Authors: Li Yang, Xiao-Yan Ma, Xiao Ruan, De-An Jiang, Cun-De Pan, Qiang Wang
Format: Article
Language:English
Published: MDPI AG 2016-04-01
Series:Molecules
Subjects:
4,8-dihydroxy-1-tetralone (4,8-DHT)
chiral-selective separation
enantiomers
phytotoxicity
Online Access:http://www.mdpi.com/1420-3049/21/4/528

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