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Dive into the research topics where Adrian Friedmann is active.

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Featured researches published by Adrian Friedmann.


Bioorganic & Medicinal Chemistry | 2009

Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part I: Discovery of the novel cereal herbicide pinoxaden

Michel Muehlebach; Manfred Boeger; Fredrik Cederbaum; Derek Cornes; Adrian Friedmann; Jutta Glock; Thierry Niderman; André Stoller; Trixie Wagner

Derivatives of the new class of 3-hydroxy-4-phenyl-5-oxo-pyrazolines were optimized towards both herbicidal activity on key annual grass weed species and selectivity in small grain cereal crops. The generic structure can be separated into three parts for the analysis of the structure-activity relationships, namely the aryl, the dione with its prodrug forms and the hydrazine moiety. Each area appears to play distinct and different roles in overall expression of biological performance which is further beneficially influenced by adjuvant response and safener action. Pinoxaden 6, a novel graminicide for use in wheat and barley incorporating a [1,4,5]oxadiazepane ring, eventually emerged as a development candidate from the discovery and optimization process.


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.


Journal of Experimental Botany | 2005

Characterization of hydrophilic and lipophilic pathways of Hedera helix L. cuticular membranes: permeation of water and uncharged organic compounds

Christian Popp; Markus Burghardt; Adrian Friedmann; Markus Riederer


Archive | 2003

Phenyl substituted heterocyclic compounds useful as herbicides

Adrian Friedmann; André Stoller; Sebastian Wendeborn


Annual Plant Reviews Volume 23: Biology of the Plant Cuticle | 2007

Transport of Lipophilic Non‐Electrolytes Across the Cuticle

Markus Riederer; Adrian Friedmann


Planta | 2005

Surface morphology and chemistry of Prunus laurocerasus L. leaves: a study using X-ray photoelectron spectroscopy, time-of-flight secondary-ion mass spectrometry, atomic-force microscopy and scanning-electron microscopy.

Mark Perkins; Clive J. Roberts; D. Briggs; Martyn C. Davies; Adrian Friedmann; Clifford Hart; Gordon Alastair Bell


Applied Surface Science | 2005

Macro and microthermal analysis of plant wax/surfactant interactions: plasticizing effects of two alcohol ethoxylated surfactants on an isolated cuticular wax and leaf model

Mark Perkins; Clive J. Roberts; D. Briggs; Martyn C. Davies; Adrian Friedmann; Clifford Hart; Gordon Alastair Bell


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


Pest Management Science | 2006

Modelling the effects of alcohol ethoxylates on diffusion of pesticides in the cuticular wax of Chenopodium album leaves

Markus Burghardt; Adrian Friedmann; Lukas Schreiber; Markus Riederer


Journal of Agricultural and Food Chemistry | 2016

Water Sorption Isotherms of Surfactants: A Tool To Evaluate Humectancy

Elisabeth Asmus; Christian Popp; Adrian Friedmann; Katja Arand; Markus Riederer

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