Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus

This publication has 12 references indexed in Scilit:

• Novel Cuticular Hydrocarbons from the Cane Beetle Antitrogus parvulus4,6,8,10,16-Penta- and 4,6,8,10,16,18-HexamethyldocosanesUnprecedented anti-anti-anti-Stereochemistry in the 4,6,8,10-Methyltetrad
  The Journal of Organic Chemistry, 2005
• Iterative Desoxypropionat‐Synthese auf der Basis einer kupfervermittelten dirigierten allylischen Substitution
  Angewandte Chemie, 2004
• Iterative Deoxypropionate Synthesis Based on a Copper‐Mediated Directed Allylic Substitution
  Angewandte Chemie International Edition, 2004
• 4,6,8,10,16-Penta- and 4,6,8,10,16,18-Hexamethyldocosanes from the Cane Beetle Antitrogus parvulus - Cuticular Hydrocarbons with Unprecedented Structure and Stereochemistry
  Organic Letters, 2003
• Regio- and stereocontrolled preparation of α-substituted phosphonocrotonate derivatives
  Tetrahedron Letters, 2002
• Cu-Catalyzed Alkylation of Grignard Reagents: A New Efficient Procedure
  Tetrahedron, 2000
• The reaction of alkyllithium reagents with Furan-3-carboxylic acid. A synthesis of 4-(Furan-3'-yl)-1-methylbutyltriphenylphosphonium iodide
  Australian Journal of Chemistry, 1984
• Prescriptions and Ingredients for Controlled CC Bond Formation with Organometallic Reagents. New synthetic methods (5)
  Angewandte Chemie International Edition, 1974
• Improved Carbon‐Carbon Linking by Controlled Copper Catalysis
  Angewandte Chemie International Edition, 1974
• Coupling of Grignard Reagents with Organic Halides
  Synthesis, 1971