Synthesis of the Four d,l-Pairs of 2-Amino-3-Phenylnorbornane-2-Carboxylic Acids

  1. Avenoza, A. 1
  2. Cativiela, C. 2
  3. Mayoral, J.A. 2
  4. Roy, M.A. 1
  1. 1 Universidad de Zaragoza
    info

    Universidad de Zaragoza

    Zaragoza, España

    GRID grid.11205.37

  2. 2 Instituto de Ciencia de Materiales de Aragón
    info

    Instituto de Ciencia de Materiales de Aragón

    Zaragoza, España

    GRID grid.466773.7

Journal:
Tetrahedron

ISSN: 0040-4020

Year of publication: 1989

Volume: 45

Issue: 12

Pages: 3923-3934

Type: Article

Export: RIS
DOI: 10.1016/S0040-4020(01)89251-6 SCOPUS: 2-s2.0-0005943255 WoS: A1989AD64900029 GOOGLE SCHOLAR

Abstract

The Diels-Alder reaction between methyl ∝-cyanocinnamate and cyclopentadiene, as a key step in the synthesis of 2-amino-3-phenylnorbornane-2-carboxylic acids, is studied. The cycloadducts can be easily separated and converted into the aminoacids through simple reactions. © 1989.