PlumX Metrics
Embed PlumX Metrics

Highly enantioselective synthesis of fluorinated γ-amino alcohols through proline-catalyzed cross-Mannich reaction

Organic Letters, ISSN: 1523-7060, Vol: 7, Issue: 16, Page: 3433-3436
2005
  • 96
    Citations
  • 0
    Usage
  • 11
    Captures
  • 0
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

Article Description

(Chemical Equation Presented) A new, simple route for the synthesis of fluorinated β-alkyl γ-amino alcohols in optically pure form in only two steps and featuring proline catalysis from inexpensive and readily available starting materials is described. The applied strategy allows for the introduction of diversity into both the β-fluoroalkyl and α-alkyl groups of these compounds. © 2005 American Chemical Society.

Bibliographic Details

Fustero, Santos; Jiménez, Diego; Sanz-Cervera, Juan F; Sánchez-Roselló, María; Esteban, Elisabet; Simón-Fuentes, Antonio

American Chemical Society (ACS)

Biochemistry, Genetics and Molecular Biology; Chemistry

Provide Feedback

Have ideas for a new metric? Would you like to see something else here?Let us know