A Route for the Total Synthesis of Enantiomerically Enriched Jasmonates 12-COOH-JA and 12-COOH-JA-Ile-Reference-Cited by-同舟云学术

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A Route for the Total Synthesis of Enantiomerically Enriched Jasmonates 12-COOH-JA and 12-COOH-JA-Ile

Published:2014-12-22 Issue:5 Volume:2015 Page:1130-1136
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Heinrich Clément F.,Widemann Emilie,Sanz Jérémie,Lugan Raphaël,Heitz Thierry,Pinot Franck,Miesch Michel,Miesch Laurence

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201403347/fullpdf

Reference32 articles.

1. Jasmonate Passes Muster: A Receptor and Targets for the Defense Hormone

2. Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany

3. The JAZ family of repressors is the missing link in jasmonate signalling

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1. Stereoselective Semi‐Hydrogenations of Alkynes by First‐Row (3d) Transition Metal Catalysts;ChemCatChem;2022-09-15

2. NO Release Inhibitory Activity of Flavonoids from Aesculus Wilsonii Seeds through MAPK (P38), NF-κB, and STAT3 Cross-Talk Signaling Pathways;Planta Medica;2022-08-29

3. Syntheses of dinor-cis/iso-12-oxo-phytodienoic acid (dn-cis/iso-OPDAs), ancestral jasmonate phytohormones of the bryophyte Marchantia polymorpha L., and their catabolites;Scientific Reports;2021-01-21

4. Stereoselective Alkyne Hydrogenation by using a Simple Iron Catalyst;ChemSusChem;2019-07-25

5. A succinct access to ω-hydroxylated jasmonates via olefin metathesis;Zeitschrift für Naturforschung C;2017-06-29

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