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Supplementary data for "synthesis and biological evaluation of highly potent fungicidal deoxy-hygrophorones"

Abstract: Based on naturally occurring hygrophorones, racemic di- and mono hydroxylated cyclopentenones bearing an aliphatic side chain have been produced in short synthetic sequences starting from furfuryl aldehyde. For the series of dihydroxylated trans-con-figured derivatives, an Ach¬matowicz and a Caddick-ring contrac¬tion were employed, and for the series of trans-configured mono-hydroxylated derivatives a Piancatelli-rearrange¬ment. All final products showed good to excellent fungicidal activities against the plant pathogens B. cinerea, S. tritici and P. infestans.

Cite this as

Leibniz Institute of Plant Biochemistry (IPB), Halle (Saale), Germany, Bette, Eileen, Sultani, Haider N., Otto, Alexander, Wessjohann, Ludger A., Arnold, Norbert, Westermann, Bernhard (2021). Dataset: Supplementary data for "synthesis and biological evaluation of highly potent fungicidal deoxy-hygrophorones". https://doi.org/10.22000/451

DOI retrieved: 2021

Additional Info

Field Value
Imported on January 12, 2023
Last update January 12, 2023
License CC BY 4.0 Attribution
Source https://doi.org/10.22000/451
Author Leibniz Institute of Plant Biochemistry (IPB), Halle (Saale), Germany
More Authors
Bette, Eileen
Sultani, Haider N.
Otto, Alexander
Wessjohann, Ludger A.
Arnold, Norbert
Westermann, Bernhard
Source Creation 2021
Publishers
Leibniz Institute of Plant Biochemistry (IPB), Halle (Saale), Germany
Production Year 2021
Publication Year 2021
Resource Type Dataset - NMR, MS, bioassay
Subject Areas
Name: Chemistry

Name: Agriculture