Total Synthesis of (2S,3S,5S,10S)- 6,9-Epoxynonadec-18-ene-7,10-diol and Formal Total Synthesis of (+)-trans-Kumausyne from d-Arabinose

This publication has 25 references indexed in Scilit:

• β-Hydroxy-γ-lactones as Chiral Building Blocks for the Enantioselective Synthesis of Marine Natural Products
  The Journal of Organic Chemistry, 2001
• Efficient Synthesis of (−)-trans-Kumausyne via Tandem Intramolecular Alkoxycarbonylation−Lactonization
  The Journal of Organic Chemistry, 1998
• Total Synthesis of (−)-trans-Kumausyne
  Tetrahedron Letters, 1995
• The Cyclodehydration Route to the Asymmetric Total Synthesis of the Marine Natural Product Isolated from the Brown Alga, Notheia Anomala
  Chemistry Letters, 1993
• General approach to halogenated tetrahydrofuran natural products from red algae of the genus Laurencia. Total synthesis of (.+-.)-trans-kumausyne and demonstration of an asymmetric synthesis strategy
  Journal of the American Chemical Society, 1991
• A Formal Total Synthesis of (6S,7S,9R,10R)-6,9-Epoxynonadec-18-ene-7,10-diol from D-Glucose
  HETEROCYCLES, 1990
• Stereocontrolled transformations of orthoester intermediates into substituted tetrahydrofurans
  Journal of the American Chemical Society, 1984
• KUMAUSYNES AND DEACETYLKUMAUSYNES, FOUR NEW HALOGENATED C-15 ACETYLENES FROM THE RED ALGA LAURENCIA NIPPONICA YAMADA
  Chemistry Letters, 1983
• KUMAUSALLENE, A NEW BROMOALLENE FROM THE MARINE RED ALGA LAURENCIA NIPPONICA YAMADA
  Chemistry Letters, 1983
• A novel lipid from the brown alga Notheia anomala
  Australian Journal of Chemistry, 1980