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Featured researches published by Ottmar Franz Hueter.


Chimia | 2016

Identification and Optimization of New Leads for Malaria Vector Control.

Ottmar Franz Hueter; Mark Hoppe; Philip Wege; Peter Maienfisch

A significant proportion of the worlds population remains at risk from malaria, and whilst great progress has been made in reducing the number of malaria cases globally through the use of vector control insecticides, these gains are under threat from the emergence of insecticide resistance. The spread of resistance in the vector populations, principally to pyrethroids, is driving the need for the development of new tools for malaria vector control. In order to identify new leads 30,000 compounds from the Syngenta corporate chemical collection were tested in a newly developed screening platform. More than 3000 compounds (10%) showed activity at ≤200 mg active ingredient (AI) litre-1 against Anopheles stephensi. Further evaluation resulted in the identification of 12 viable leads for the control of adult mosquitoes, most originating from current or former insecticide projects. Surprisingly, one of these leads emerged from a former PPO herbicide project and one from a former complex III fungicide project. This indicates that representatives of certain herbicide and fungicide projects and modes of action can also represent a valuable source of leads for malaria vector control. Optimization of the diphenyl ether lead 1 resulted in the identification of the cyano-pyridyl compound 31. This compound 31 exhibits good activity against mosquito species including rdl resistant Anopheles. It is only slightly weaker than permethrin and does not show relevant levels of cross-resistance to the organochlorine insecticide dieldrin.


Archive | 2008

Spiroheterocyclic pyrrolidine dione derivatives useful as pesticides

Werner Zambach; Ottmar Franz Hueter; Jean Wenger; Marcela Goeghova; Thomas Pitterna; Peter Maienfisch; Michel Muehlebach


Archive | 2014

Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents

Andrew Edmunds; Michel Muehlebach; André Stoller; Olivier Loiseleur; Anke Buchholz; Ottmar Franz Hueter; Aurelien Bigot; Roger Graham Hall; Daniel Emery; Pierre Joseph Marcel Jung; Long Lu; Yaming Wu; Ruifang Chen


Archive | 2012

1,2,3 triazole pesticides

Pierre Joseph Marcel Jung; Ottmar Franz Hueter; Peter Renold; Thomas Pitterna


Archive | 2010

4-CYANO-3-BENZOYLAMINO-N-PHENYL-BENZAMIDES FOR USE IN PEST CONTROL

Pierre Joseph Marcel Jung; Christopher Richard Ayles Godfrey; Ottmar Franz Hueter; Peter Maienfisch


Archive | 2008

TROPANE DERIVATIVES USEFUL AS PESTICIDES

Patrice Selles; Eric Daniel Clarke; Alison Clare Elliot; Delphine Fawke; Ottmar Franz Hueter; Urs Mueller; Peter Renold; Sarah Margaret Targett; William Guy Whittingham


Archive | 2005

Avermectin And Avermectin Monosaccharide Substituted In The 4"- And 4" Position Respectively

Pierre Jung; Thomas Pitterna; Fiona Murphy Kessabi; Laura Quaranta; Ottmar Franz Hueter


Archive | 2009

Insecticidal combinations comprising abamectin and cyflumetofen

Peter Maienfisch; Max Angst; Ottmar Franz Hueter; Jorges Cisneros; Paulo Aramaki; Alfred Rindlisbacher


Archive | 2003

Avermectin b1 and avermectin b1 monosaccharide derivatives having an alkoxymethyl substituent in the 4"-or 4'-position

Peter Maienfisch; Fiona Murphy Kessabi; Jérôme Yves Cassayre; Laura Quaranta; Thomas Pitterna; Ottmar Franz Hueter; Pierre Jung


Archive | 2014

Pesticidally active substituted 5,5-bicyclic heterocycles with sulphur containing substituents

Michel Muehlebach; Andrew Edmunds; André Stoller; Natalie Anne Miller; Ottmar Franz Hueter

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