A
Anne Eeg Jensen
Researcher at Ludwig Maximilian University of Munich
Publications - 14
Citations - 491
Anne Eeg Jensen is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Coupling reaction & Aryl. The author has an hindex of 7, co-authored 14 publications receiving 483 citations.
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Journal ArticleDOI
Nickel-catalyzed cross-coupling between functionalized primary or secondary alkylzinc halides and primary alkyl halides
Anne Eeg Jensen,Paul Knochel +1 more
TL;DR: In the presence of Bu(4)NI (3 equiv) and 4-fluorostyrene (20 mol %), unreactive primary and secondary alkylzinc iodides undergo nickel-catalyzed cross-couplings with various primaryAlkyl iodides or bromides allowing the synthesis of aminated products.
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New Efficient Nickel- and Palladium-Catalyzed Cross-Coupling Reactions Mediated by Tetrabutylammonium Iodide
TL;DR: The addition of Bu4NI has been found to accelerate the palladium(0)-catalyzed cross-coupling between benzylic zinc bromides and aryl or alkenyl triflates leading to polyfunctional products in good yields under mild reaction conditions.
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Preparation and Reactions of Functionalized Arylmagnesium Reagents
TL;DR: The iodine-magnesium exchange, represent a unique method for the preparation of aryl and heteroaryl magnesium reagents that can be either trapped directly with aldehydes or transmetallated to copper or zinc to participate in cross-coupling reactions.
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Preparation of polyfunctional heterocycles using highly functionalized aminated arylmagnesium reagents as versatile scaffolds.
TL;DR: Functionalized Grignard reagents, derived from readily available o-iodoaniline derivatives and obtained via a straightforward iodine-magnesium exchange, can be used to prepare a wide range of polyfunctional indoles, quinolines, and quinazolinones.
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Improved nickel-catalyzed cross-coupling reaction conditions between ortho-substituted aryl iodides/nonaflates and alkylzinc iodides in solution and in the solid-phase
TL;DR: In this paper, aryl iodides and nonaflates undergo nickel-catalyzed cross-coupling reactions with functionalized alkylzinc iodides in the solid-phase as well as in solution providing high HPLC purities and good yields.