Asymmetric Synthesis of a Constituent of Iris Essential Oil by Homoenolate Alkylation of a Chiral Bicyclic Lactam

This publication has 7 references indexed in Scilit:

• Chiral bicyclic Lactams as homoenolate equivalents: An asymmetric route to 5-substituted cyclohexenones
  Tetrahedron, 1997
• Preparation of optically active cyclohexenones: Chirons for the lipophilic moiety of flowery‐ and woody‐like odorant ketones
  Helvetica Chimica Acta, 1993
• Enantioselective conjugate addition to cyclic enones with scalemic lithium organo(amido)cuprates, Part IV. Relationship between ligand structure and enantioselectivity
  Tetrahedron, 1993
• Asymmetric reduction of the prochiral carbonyl group of aliphatic .gamma.- and .delta.-keto acids by use of fermenting bakers' yeast
  The Journal of Organic Chemistry, 1987
• Facile regioselective formation of thiopeptide linkages from oligopeptides with new thionation reagents
  Tetrahedron Letters, 1983
• Preparation of functionalized ketones via low temperature grignard reaction
  Tetrahedron Letters, 1980
• Etudes sur les matières végétales volatiles XC. Présence d' apocynine (acéto‐vanillone) dans l'huile essentielle d'iris
  Helvetica Chimica Acta, 1949