The absolute configuration of the side chain diol moiety of the poison-frog alkaloid pumiliotoxin B

This publication has 5 references indexed in Scilit:

• The structure of the side chain of the frog alkaloid pumiliotoxin B
  Tetrahedron Letters, 1982
• Highly stereocontrolled reduction of α′-alkoxyenones to give either the threo or eryhtro allylic 1,2-diol. Assignment of the threo configuration to the C-15, C-16 diol of pumiliotoxin B.1
  Tetrahedron Letters, 1982
• Synthesis of N-benzoyl-L-daunosamine from D-threonine
  Tetrahedron Letters, 1981
• A new class of indolizidine alkaloids from the poison frog, Dendrobates tricolor. X-ray analysis of 8-hydroxy-8-methyl-6-(2'-methylhexylidene)-1-azabicyclo[4.3.0]nonane
  Journal of the American Chemical Society, 1980
• Froschgifte. Isolierung und Struktur von Pumiliotoxin C
  European Journal of Organic Chemistry, 1969