4.5 Review

Synthetic Approaches to Coronafacic Acid, Coronamic Acid, and Coronatine

Journal

SYNTHESIS-STUTTGART
Volume 48, Issue 20, Pages 3429-3448

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0035-1562552

Keywords

agrochemistry; asymmetric synthesis; bicyclic compounds; carbocycles; stereochemistry; total synthesis

Funding

  1. University of Strathclyde
  2. Syngenta

Ask authors/readers for more resources

The phytotoxin coronatine (COR) is a functional mimic of the active plant hormone (+)-7-iso-jasmonoyl-L-isoleucine (JA-IIe), which regulates stress responses. Structurally, COR is composed of a core unit, coronafacic acid (CFA), which is connected to coronamic acid (CMA), via an amide linkage. COR has been found to induce a range of biological activity in plants and based on its biological profile, COR, as well as CFA, and CMA are attractive starting points for agrochemical discovery, resulting in numerous total synthesis efforts. This review will discuss the synthetic approaches towards CFA, CMA and, ultimately COR, to date. 1 Introduction 2 Total Synthesis of Coronafacic Acid (CFA, 4) 2.1 Mapping Synthetic Strategies 2.2 Intermolecular Diels-Alder Approaches 2.3 Intramolecular Diels-Alder Approaches 2.4 Conjugate Addition Approaches 2.5 Haller-Bauer Approaches 2.6 Intramolecular Cyclisation Approaches 2.7 Oxy-Cope Approaches 3 Total Synthesis of Coronamic Acid (CMA, 5) 3.1 Mapping Synthetic Strategies 3.2 Final Installation of C-1 3.3 Final Installation of C-2 3.4 Final Installation of C-3 4 Total Synthesis of Coronatine (COR, 1) 5 Conclusions

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available