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Dive into the research topics where Thomas Maetzke is active.

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Featured researches published by Thomas Maetzke.


Pest Management Science | 2011

Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: Chemistry and biology of the cereal herbicide pinoxaden†

Michel Muehlebach; Fredrik Cederbaum; Derek Cornes; Adrian Friedmann; Jutta Glock; Gavin John Hall; Adriano Indolese; Daniel P. Kloer; Gael Le Goupil; Thomas Maetzke; Hans Meier; Rudolf Schneider; André Stoller; Henry Szczepanski; Sebastian Wendeborn; Hansjuerg Widmer

BACKGROUND Pinoxaden is a new cereal herbicide that provides outstanding levels of post-emergence activity against a broad spectrum of grass weed species for worldwide selective use in both wheat and barley. RESULTS Factors influencing activity and tolerance to pinoxaden were in part linked to distinct structural parts of the active ingredient. Three complementary contributions that decisively impact upon the herbicidal potency against grasses were identified: a preferred 2,6-diethyl-4-methyl aromatic substitution pattern, a dione area suitable for proherbicide formation and beneficial adjuvant effects. The uptake and translocation pattern of pinoxaden when coapplied with its tailored adjuvant were analysed by autoradiography, indicating extensive and rapid penetration, followed by effective distribution throughout the plant. Crop injury reduction on incorporation of the [1,4,5]oxadiazepane ring into the aryldione template was reinforced with safener technology. Comparative studies on the behaviour of pinoxaden applied either alone or in combination with the safener cloquintocet-mexyl demonstrated that addition of the safener resulted in significant enhancement of metabolic degradation in wheat and barley, providing excellent crop tolerance and a substantial selectivity margin without adverse effects on weed control. CONCLUSION The biological potential of pinoxaden and its active principle pinoxaden dione in terms of grass weed control and tolerance in cereals was fully exploited by inclusion of the safener cloquintocet-mexyl in the formulation in combination with a specific and tailor-made tank-mix adjuvant based on methylated rape seed oil.


Archive | 1999

Herbicidally active 3-hydroxy-4-aryl-5-oxopyrazoline derivatives

Michel Mühlebach; Jutta Glock; Thomas Maetzke; André Stoller


Pesticide Chemistry: Crop Protection, Public Health, Environmental Safety | 2007

Discovery and SAR of Pinoxaden: A New Broad Spectrum, Postemergence Cereal Herbicide

Michel Muehlebach; Hans-Georg Brunner; Fredrik Cederbaum; Thomas Maetzke; René Mutti; Anita Schnyder; André Stoller; Sebastian Wendeborn; Jean Wenger; Peter Boutsalis; Derek Cornes; Adrian Friedmann; Jutta Glock; Urs Hofer; Stephen Hole; Thierry Niderman; Marco Quadranti


Synlett | 2006

A Convenient Protocol for the Synthesis of Hindered Aryl Malononitriles

Anita Schnyder; Adriano Indolese; Thomas Maetzke; Jean Wenger; Hans-Ulrich Blaser


Archive | 2000

Process for the preparation of herbicidal derivatives

Thomas Maetzke; René Mutti; Henry Szczepanski


Archive | 1999

3-hydroxy-4-aryl-5-pyrazoline derivatives as herbicides

Michel Mühlebach; Jutta Glock; Thomas Maetzke; André Stoller


Archive | 2000

p-tolyl-heterocycles as herbicides

Thomas Maetzke; André Stoller; Henry Szczepanski; Sebastian Wendeborn


Archive | 2000

A process for the preparation of herbicides

Thomas Maetzke; René Mutti; Henry Szczepanski


Archive | 2000

Verfahren zur herstellung von herbiziden

Thomas Maetzke; René Mutti; Henry Szczepanski


Archive | 2000

Neue Herbizide New Herbicides

Thomas Maetzke; André Stoller; Sebastian Wendeborn; Henry Szczepanski

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