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Ficini Reaction with Acrylates for the Stereoselective Synthesis of Aminocyclobutanes.
Robert, Emma G L; Waser, Jerome.
Affiliation
  • Robert EGL; Ecole Polytechnique Federale de Lausanne, ISIC, SWITZERLAND.
  • Waser J; Ecole Polytechnique Federale de Lausanne, ISIC - Laboratory of Catalysis and Organic Synthesis, EPFL BCH 4306 Batiment chimie UNIL, 1015, Lausanne, SWITZERLAND.
Chemistry ; : e202401810, 2024 Jun 13.
Article in En | MEDLINE | ID: mdl-38869382
ABSTRACT
The first Ficini reaction between ynamides and acrylates is reported herein. The reaction is catalyzed by B(C6F5)3 acting as a Lewis acid and is giving access to stable tri-substituted aminocyclobutenes in high yield. The resulting products can be hydrogenated and epimerized under basic conditions or in presence of a Lewis acid, providing two distinct trans- aminocyclobutane monoester stereoisomers in high yield and diastereoisomeric ratio (up to quantitative yield and >991 dr).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Switzerland