38239-01-9Relevant academic research and scientific papers
Heterocyclic Compounds as Pesticides
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Paragraph 0365; 0366; 0367, (2017/12/27)
The present application relates to novel heterocyclic compounds of the formula (I) in which G, R1, R2, Q and V have the meanings given in the description, to processes for their preparation and to their use for controlling animal pests.
HETEROCYCLIC COMPOUNDS AS PEST CONTROL AGENTS
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Paragraph 0417-0419, (2016/06/01)
The present application relates to the use of known and novel heterocyclic compounds for controlling animal pests, to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests.
Mild and rapid Pd-catalyzed cross-coupling with hydrazine in continuous flow: Application to the synthesis of functionalized heterocycles
Deangelis, Andrew,Wang, Dong-Hui,Buchwald, Stephen L.
supporting information, p. 3434 - 3437 (2013/05/09)
Minimizing risk: The synthesis of arylhydrazines through C?￡?N cross-coupling of aryl chlorides with hydrazine is described. Through the use of continuous flow, the hazards associated with the use of hydrazine in the presence of transition metals are decreased. In addition, multistep flow sequences have also been developed for the generation of functionalized heterocycles utilizing the arylhydrazine intermediates.
NOVEL CATALYSTS
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Page/Page column 58-59, (2012/06/01)
The present invention provides novel compounds and ligands that are useful in transition metal catalyzed cross-coupling reactions. For example, the compounds and ligands of the present invention are useful in palladium or gold catalyzed cross-coupling reactions.
Palladium-catalyzed cross-coupling of aryl chlorides and tosylates with hydrazine
Lundgren, Rylan J.,Stradiotto, Mark
supporting information; experimental part, p. 8686 - 8690 (2011/01/08)
Hydrazine is not a problem anymore: The title transformation is the first reaction to yield aryl hydrazines through the cross-coupling of aryl chlorides and tosylates with hydrazine. An appropriately designed palladium catalyst allows this reaction to proceed rapidly under mild conditions, and with excellent chemoselectivity (see scheme; Ad=adamantyl, Ts=4-toluenesulfonyl).
