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Chemoselective Reductive Aminations in Aqueous Nanoreactors Using Parts per Million Level Pd/C Catalysis.
Thakore, Ruchita R; Takale, Balaram S; Casotti, Gianluca; Gao, Eugene S; Jin, Henry S; Lipshutz, Bruce H.
Afiliação
  • Thakore RR; Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States.
  • Takale BS; Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States.
  • Casotti G; Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States.
  • Gao ES; Dipartimento di Chimica e Chimica Industriale, Universitá di Pisa, Via G. Moruzzi 13, 56124 Pisa, Italy.
  • Jin HS; Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States.
  • Lipshutz BH; Princeton International School of Mathematics and Science, 19 Lambert Drive, Princeton, New Jersey 08540, United States.
Org Lett ; 22(16): 6324-6329, 2020 08 21.
Article em En | MEDLINE | ID: mdl-32806206
Condensation in recyclable water between aldehydes or ketones and amines occurs smoothly within the hydrophobic cores of nanomicelles, resulting in imine formation that is subject to subsequent reduction leading, overall, to reductive amination. This micellar technology enables the synthesis of several types of pharmaceuticals, a new procedure that relies on only 2000 ppm (0.20 mol %) palladium from commercially available Pd/C. A broad range of substrates can be used under mild conditions, leading to high chemical yields of the desired secondary and tertiary amines.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article