Studies directed towards the asymmetric total synthesis of antileukemic lignan lactones —synthesis of (−)-podorhizon—

This publication has 9 references indexed in Scilit:

• Synthetic studies on lignan lactones: aryl dithiane route to (.+-.)-podorhizol and (.+-.)-isopodophyllotoxone and approaches to the stegane skeleton
  The Journal of Organic Chemistry, 1978
• Phosphonate Ester Preparation from Active Methylene Compounds and Phosphorochloridate Esters
  Synthesis, 1978
• A short synthesis of (.+-.)-isostegane
  The Journal of Organic Chemistry, 1976
• Stereochemical studies—XXX
  Tetrahedron, 1974
• Configurational equilibria in 2,4-disubstituted-γ-butyrolactones
  Journal of the Chemical Society, Chemical Communications, 1974
• The Absolute Configurations of Thujaplicatin Methyl Ether and 2-(3, 4, 5-Trimethoxybenzyl)-3-(3, 4-methylenedioxybenzyl) butyrolactone
  YAKUGAKU ZASSHI, 1974
• Tumor inhibitors. LXXXX. Steganacin and steganangin, novel antileukemic lignan lactones from Steganotaenia araliacea
  Journal of the American Chemical Society, 1973
• Antitumor Activity of Bursera schlechtendalii (Burseraceae): Isolation and Structure Determination of Two New Lignans
  Journal of Pharmaceutical Sciences, 1972
• Podophyllum‐ Lignane: Struktur und Absolutkonfiguration von Podorhizol‐β‐D‐glucosid ( = Lignan F). 19. Mitt. über mitosehemmende Naturstoffe [1]
  Helvetica Chimica Acta, 1967