Understanding the Activity and Enantioselectivity of Acetyl-Protected Aminoethyl Quinoline Ligands in Palladium-Catalyzed ß-C(sp<sup>3</sup>)-H Bond Arylation Reactions.

Romero, Erik A; Chen, Gang; Gembicky, Milan; Jazzar, Rodolphe; Yu, Jin-Quan; Bertrand, Guy

Understanding the Activity and Enantioselectivity of Acetyl-Protected Aminoethyl Quinoline Ligands in Palladium-Catalyzed ß-C(sp³)-H Bond Arylation Reactions.

Romero, Erik A; Chen, Gang; Gembicky, Milan; Jazzar, Rodolphe; Yu, Jin-Quan; Bertrand, Guy.

Afiliação

Romero EA; UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093-0358 , United States.
Chen G; Department of Chemistry , The Scripps Research Institute , 10550 N. Torrey Pines Road , La Jolla , California 92037 , United States.
Gembicky M; UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093-0358 , United States.
Jazzar R; UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093-0358 , United States.
Yu JQ; Department of Chemistry , The Scripps Research Institute , 10550 N. Torrey Pines Road , La Jolla , California 92037 , United States.
Bertrand G; UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093-0358 , United States.

J Am Chem Soc ; 141(42): 16726-16733, 2019 10 23.

Article em En | MEDLINE | ID: mdl-31565934

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Am Chem Soc Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

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