Synthesis of Enantiopure Quaternary Prolines by a Metathesis Process of 2,5-Ethenoproline Derivatives

  1. Carreras, J. 1
  2. Avenoza, A. 1
  3. Busto, J.H. 1
  4. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    GRID grid.119021.a

Journal:
Synthesis (Stuttgart)

ISSN: 0039-7881

Year of publication: 2010

Volume: 19

Pages: 3353-3357

Type: Article

Export: RIS
DOI: 10.1055/s-0030-1257907 SCOPUS: 2-s2.0-77957123339 WoS: 000282106600020 GOOGLE SCHOLAR

Metrics

Cited by

  • Scopus Cited by: 3 (12-06-2021)

Journal Citation Reports

  • Year 2010
  • Journal Impact Factor: 2.26
  • Best Quartile: Q2
  • Area: CHEMISTRY, ORGANIC Quartile: Q2 Rank in area: 24/56 (Ranking edition: SCIE)

SCImago Journal Rank

  • Year 2010
  • SJR Journal Impact: 1.2
  • Best Quartile: Q1
  • Area: Organic Chemistry Quartile: Q1 Rank in area: 43/174
  • Area: Catalysis Quartile: Q3 Rank in area: 21/40

Abstract

A novel azabicyclic amino acid was synthesized in both enantiopure forms. The ring-opening metathesis of methyl N-(tert-butoxycarbonyl)-7-azabicyclo[2.2. 1]hept-2-ene-1-carboxylates was used as a method for accessing a new family of enantiopure proline analogues. © Georg Thieme Verlag Stuttgart New York.