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α-Aminoboronates: recent advances in their preparation and synthetic applications.
Ming, Wenbo; Soor, Harjeet S; Liu, Xiaocui; Trofimova, Alina; Yudin, Andrei K; Marder, Todd B.
Afiliación
  • Ming W; Institute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. todd.marder@uni-wuerzburg.de.
  • Soor HS; Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 Saint George Street, Toronto, Ontario M5S 3H6, Canada. andrei.yudin@utoronto.ca.
  • Liu X; Institute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. todd.marder@uni-wuerzburg.de.
  • Trofimova A; Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 Saint George Street, Toronto, Ontario M5S 3H6, Canada. andrei.yudin@utoronto.ca.
  • Yudin AK; Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 Saint George Street, Toronto, Ontario M5S 3H6, Canada. andrei.yudin@utoronto.ca.
  • Marder TB; Institute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. todd.marder@uni-wuerzburg.de.
Chem Soc Rev ; 50(21): 12151-12188, 2021 Nov 01.
Article en En | MEDLINE | ID: mdl-34585200
ABSTRACT
α-Aminoboronic acids and their derivatives are useful as bioactive agents. Thus far, three compounds containing an α-aminoboronate motif have been approved by the Food and Drug Administration (FDA) as protease inhibitors, and more are currently undergoing clinical trials. In addition, α-aminoboronic acids and their derivatives have found applications in organic synthesis, e.g. as α-aminomethylation reagents for the synthesis of chiral nitrogen-containing molecules, as nucleophiles for preparing valuable vicinal amino alcohols, and as bis-nucleophiles in the construction of valuable small molecule scaffolds. This review summarizes new methodology for the preparation of α-aminoboronates, including highlights of asymmetric synthetic methods and mechanistic explanations of reactivity. Applications of α-aminoboronates as versatile synthetic building blocks are also discussed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estereoisomerismo País/Región como asunto: America do norte Idioma: En Revista: Chem Soc Rev Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estereoisomerismo País/Región como asunto: America do norte Idioma: En Revista: Chem Soc Rev Año: 2021 Tipo del documento: Article País de afiliación: Alemania