HIGHLY STEREOSELECTIVE CONSTRUCTION OF CHIRAL QUATERNARY CARBON: ASYMMETRIC SYNTHESIS OF β,β-DISUBSTITUTED γ-BUTYROLACTONES

This publication has 14 references indexed in Scilit:

• On the stereoselectivity of the α-alkylation of β-hydroxy esters. Enantioselective synthesis of 4,4- and 6,6-disubstituted cyclohex-2-en-1-ones.
  Tetrahedron Letters, 1981
• Enantioselective synthesis of (−)-velbanamine and (+)-isovelbanamine using L-glutamic acid as chiral template
  Tetrahedron Letters, 1980
• Asymmetric synthesis of 1,2-disubstituted cycloalkanecarboxaldehydes. procedures for the highly stereoselective preparation of cis- and trans-isomer
  Tetrahedron Letters, 1980
• Asymmetric total synthesis of the antileukaemic lignan precursor (-)steganone and revision of its absolute configuration
  Tetrahedron Letters, 1980
• Methodology for the construction of quaternary carbon centers
  Tetrahedron, 1980
• First asymmetric total synthesis of (+)-steganacin determination of absolute stereochemistry
  Tetrahedron Letters, 1980
• Stereoselective reactions. III. A highly efficient method for the asymmetric synthesis of 2-alkylcycloalkanones via chiral chelated lithioenamines.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1979
• Recent advances in asymmetric synthesis
  Tetrahedron, 1979
• Effective Catalytic Asymmetric Synthesis of S-(—)-3-Methoxycarbonyl-4-(3,4-methylenedioxyphenyl)butanoic Acid. A Simple and Effective Route to Chiral Lignans
  HETEROCYCLES, 1979
• Asymmetric carbon-carbon bond formation from chiral oxazolines
  Accounts of Chemical Research, 1978