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Stereoselective Syntheses of Masked ß-Amino Acid Containing Phthalides.
Serusi, Lorenzo; Zebrowski, Paul; Schörgenhumer, Johannes; Massa, Antonio; Waser, Mario.
Afiliación
  • Serusi L; Institute of Organic Chemistry, Johannes Kepler University Linz, Altenbergerstr. 69, AT-4040 Linz, Austria.
  • Zebrowski P; Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno, Via Giovanni Paolo II, IT-84084-Fisciano (SA), Italy.
  • Schörgenhumer J; Institute of Organic Chemistry, Johannes Kepler University Linz, Altenbergerstr. 69, AT-4040 Linz, Austria.
  • Massa A; Department of Chemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
  • Waser M; Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno, Via Giovanni Paolo II, IT-84084-Fisciano (SA), Italy.
Helv Chim Acta ; 105(11): e202200110, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36845268
ABSTRACT
We herein report a protocol for the asymmetric aldol-initiated cascade addition of isoxazolidin-5-ones to ortho-cyanobenzaldehydes by using Takemoto's bifunctional organocatalyst. This approach allows for the synthesis of various novel ß2,2-amino acid-phthalide conjugates with good enantio- and diastereoselectivities in reasonable yields and the further ring-opening of these compounds to acyclic carboxylic acid derivatives was demonstrated too.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Helv Chim Acta Año: 2022 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Helv Chim Acta Año: 2022 Tipo del documento: Article País de afiliación: Austria