Controlling benzylic functionality and stereochemistry: 1. Synthesis of the secopseudopterosin aglycone

This publication has 16 references indexed in Scilit:

• Synthesis of (±)-dihydroxyserrulatic acid via (arene)chromium complexes
  Tetrahedron Letters, 1990
• Enantiospecific total synthesis of pseudopterosins A and E
  Journal of the American Chemical Society, 1989
• Recent Advancements in the Reformatsky Reaction
  Synthesis, 1989
• Total synthesis of (-)-pseudopterosin A
  The Journal of Organic Chemistry, 1988
• Directed Homogeneous Hydrogenation [New Synthetic Methods (65)]
  Angewandte Chemie International Edition in English, 1987
• The seco-pseodopteosins, new anti-inflammaytory diterpene-glycosides from a caribbean gorgonian octocoral of the genus
  Tetrahedron, 1987
• The pseudopterosins: a new class of antiinflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia)
  The Journal of Organic Chemistry, 1986
• The pseudopterosins: anti-inflammatory and analgesic natural products from the sea whip Pseudopterogorgia elisabethae.
  Proceedings of the National Academy of Sciences, 1986
• The chemistry of Eremophila spp. XVI. New serrulatanes from Eremophila spp.
  Australian Journal of Chemistry, 1981
• Stereochemical control of reductions. IV. Control of hydrogenation stereochemistry by intramolecular anionic coordination to homogeneous catalysts
  Journal of the American Chemical Society, 1974