Literature DB >> 35482871

Accelerating reaction generality and mechanistic insight through additive mapping.

Cesar N Prieto Kullmer1, Jacob A Kautzky1, Shane W Krska2, Timothy Nowak3, Spencer D Dreher2, David W C MacMillan1.   

Abstract

Reaction generality is crucial in determining the overall impact and usefulness of synthetic methods. Typical generalization protocols require a priori mechanistic understanding and suffer when applied to complex, less understood systems. We developed an additive mapping approach that rapidly expands the utility of synthetic methods while generating concurrent mechanistic insight. Validation of this approach on the metallaphotoredox decarboxylative arylation resulted in the discovery of a phthalimide ligand additive that overcomes many lingering limitations of this reaction and has important mechanistic implications for nickel-catalyzed cross-couplings.

Entities:  

Year:  2022        PMID: 35482871     DOI: 10.1126/science.abn1885

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  3 in total

1.  Decarboxylative Cross-Coupling: A Radical Tool in Medicinal Chemistry.

Authors:  Gabriele Laudadio; Maximilian D Palkowitz; Tamara El-Hayek Ewing; Phil S Baran
Journal:  ACS Med Chem Lett       Date:  2022-08-10       Impact factor: 4.632

2.  Screening for generality in asymmetric catalysis.

Authors:  Corin C Wagen; Spencer E McMinn; Eugene E Kwan; Eric N Jacobsen
Journal:  Nature       Date:  2022-09-01       Impact factor: 69.504

3.  Control of Redox-Active Ester Reactivity Enables a General Cross-Electrophile Approach to Access Arylated Strained Rings.

Authors:  Daniel C Salgueiro; Benjamin K Chi; Ilia A Guzei; Pablo García-Reynaga; Daniel J Weix
Journal:  Angew Chem Int Ed Engl       Date:  2022-07-05       Impact factor: 16.823

  3 in total

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