Synthesis 2018; 50(19): 3936-3946
DOI: 10.1055/s-0037-1610440
paper
© Georg Thieme Verlag Stuttgart · New York

Sulfonamides as Amine Component in the Petasis-Borono Mannich Reaction: A Concise Synthesis of α-Aryl- and α-Alkenylglycine Derivatives­

Andreas M. Diehl
Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Strasse 54, 67663 Kaiserslautern, Germany   Email: manolikakes@chemie.uni-kl.de
,
Omar Ouadoudi
Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Strasse 54, 67663 Kaiserslautern, Germany   Email: manolikakes@chemie.uni-kl.de
,
Eleni Andreadou
Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Strasse 54, 67663 Kaiserslautern, Germany   Email: manolikakes@chemie.uni-kl.de
,
Department of Chemistry, TU Kaiserslautern, Erwin-Schrödinger-Strasse 54, 67663 Kaiserslautern, Germany   Email: manolikakes@chemie.uni-kl.de
› Author Affiliations
This work was financially supported by the Fonds der Chemischen Industrie­ (Liebig Fellowship to G. M.).
Further Information

Publication History

Received: 13 April 2018

Accepted after revision: 30 May 2018

Publication Date:
18 July 2018 (online)


Abstract

A catalyst-free three-component synthesis of α-aryl- and α-alkenylglycine derivatives starting from glyoxylic acid, sulfonamides, and aryl- or alkenylboronic acids is described. This operationally simple method tolerates a broad range of functional groups and enables the generation of a wide array of α-amino acids. Sulfonamides were utilized as amine component in the classic Petasis reaction for the first time.

Supporting Information

 
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