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Dive into the research topics where Jürgen Harry Schaetzer is active.

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Featured researches published by Jürgen Harry Schaetzer.


Bioorganic & Medicinal Chemistry Letters | 2014

Efficient synthesis of fused bicyclic ethers and their application in herbicide chemistry.

Jürgen Harry Schaetzer; Andrew Edmunds; Katharina Gaus; Stefano Rendine; Alain De Mesmaeker; Willy Thaddaeus Rueegg

A series of triketones 2 and 3 featuring novel fused bicyclic aryl ethers have been prepared. The syntheses utilized ring-closing olefin metathesis (compounds 2), or oxidative cyclization of allylphenols as the key steps. The herbicidal activity of the targeted triketones 2 and 3 on various grasses and broad-leaved weeds was determined and compared with compound 1. The strength of the novel compounds 2 and 3 is their good herbicidal activity on broad-leaved weeds in post-emergent applications, whereas activity on grasses was inferior compared to 1. In addition, computational methods have been applied to provide a deeper understanding of the SAR found for compounds 2 and 3.


Pest Management Science | 2018

The importance of trifluoromethyl pyridines in crop protection: Trifluoromethyl pyridines in crop protection

Adam Burriss; Andrew Edmunds; Daniel Emery; Roger Graham Hall; Olivier Jacob; Jürgen Harry Schaetzer

The pyridine ring, substituted by a trifluoromethyl substituent has been successfully incorporated into molecules with useful biological properties. During the period 1990 to September 2017, 14 crop protection products bearing a trifluoromethyl pyridine have been commercialized or proposed for an ISO common name, covering fungicides, herbicides, insecticides and nematicides. Chemical processes have been developed to provide trifluoromethyl pyridine intermediates, from non-fluorinated pyridine starting materials, at scale and with affordable costs of goods. These attractive starting materials were readily adopted by research chemists, and elaborated through simple chemical modifications into new active ingredients. In a second approach, substituted trifluoromethyl pyridine rings have been constructed from acyclic, trifluoromethyl starting materials, which again has served to identify new active ingredients. Molecular matched pair analysis reveals subtle, yet important differences in physicochemical and agronomic properties of trifluoromethyl pyridines compared with the phenyl analogues. This review focuses on the past 27 years, seeking to identify reasons behind the success of such research programmes, and inspire the search for new crop protection chemicals containing the trifluoromethyl pyridine ring.


Archive | 2001

Substituted pyridine herbicides

Andrew Edmunds; Alain De Mesmaeker; Christoph Lüthy; Jürgen Harry Schaetzer


Archive | 1999

Pyridine ketones useful as herbicides

Andrew Edmunds; Karl Seckinger; Christoph Lüthy; Walter Kunz; Mesmaeker Alain De; Jürgen Harry Schaetzer


Archive | 2005

Substituted bicyclooctenes and their use as herbicides

Renaud Beaudegnies; Christoph Lüthy; Andrew Edmunds; Jürgen Harry Schaetzer; Sebastian Wendeborn


Archive | 2010

Spiro fused 1 -amino - piperidine pyrrolidine dione derivatives with pesticidal activity

Thomas Pitterna; Michel Muehlebach; Jürgen Harry Schaetzer


Archive | 2003

HERBICIDALLY ACTIVE HETEROCYCLYLALKYNES

Jürgen Harry Schaetzer; Jean Wenger; Sabine Berteina-Raboin; Kurt Nebel; André Stoller; Roger Graham Hall


Archive | 2011

Spiroheterocyclic pyrrolidine derivatives based pesticides

Michel Muehlebach; Jürgen Harry Schaetzer


Archive | 2010

New spiroheterocyclic furan and thiofuran dione derivatives

Jürgen Harry Schaetzer; Thomas Pitterna; Long Lu; Yaming Wu; Peter Renold; Francesca Perruccio; Jérôme Yves Cassayre; Michel Mueglebach


Archive | 2010

Chemical compounds and their use as pesticides

Thomas Pitterna; Michel Muehlebach; Jürgen Harry Schaetzer

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