Literature DB >> 18491343

A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles.

Kelvin L Billingsley1, Stephen L Buchwald.   

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Year:  2008        PMID： 18491343      PMCID： PMC2748766          DOI： 10.1002/anie.200801465

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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5.  Total synthesis of (+/-)-cytisine.

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6.  Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure.

Authors:  Timothy E Barder; Shawn D Walker; Joseph R Martinelli; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2005-04-06       Impact factor: 15.419

7.  The First Phosphine Oxide Ligand Precursors for Transition Metal Catalyzed Cross-Coupling Reactions: C-C, C-N, and C-S Bond Formation on Unactivated Aryl Chlorides.

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Journal:  Angew Chem Int Ed Engl       Date:  2001-04-17       Impact factor: 15.336

8.  Discovery of 4-{4-[3-(pyridin-2-yl)-1H-pyrazol-4-yl]pyridin-2-yl}-N-(tetrahydro-2H- pyran-4-yl)benzamide (GW788388): a potent, selective, and orally active transforming growth factor-beta type I receptor inhibitor.

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9.  Efficient Stille cross-coupling reaction using aryl chlorides or bromides in water.

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10.  Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of potassium aryl- and heteroaryltrifluoroborates.

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2.  Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol esters.

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3.  Nickel-Catalyzed Suzuki-Miyaura Coupling of Aliphatic Amides.

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4.  A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.

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7.  A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates.

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8.  Rh(I)-catalyzed direct arylation of pyridines and quinolines.

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9.  A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

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10.  Scope of the Suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroborates.

Authors:  Gary A Molander; Belgin Canturk; Lauren E Kennedy
Journal:  J Org Chem       Date:  2009-02-06       Impact factor: 4.354
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