Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology

This publication has 14 references indexed in Scilit:

• Chiral Synthesis via Organoboranes. 44. Racemic and Diastereo- and Enantioselective Homoallenylboration Using Dialkyl 2,3-Butadien-1-ylboronate Reagents. Another Novel Application of the Tandem Homologation−Allylboration Strategy
  The Journal of Organic Chemistry, 1996
• Catalytic Asymmetric Dihydroxylation
  Chemical Reviews, 1994
• Reaction of diazomethane with clerocidin. Preparation of new clerodane diterpenoid derivatives
  Tetrahedron Letters, 1993
• High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
  Journal of the American Chemical Society, 1991
• Asymmetric synthesis using tartrate ester modified allylboronates. 1. Factors influencing stereoselectivity
  The Journal of Organic Chemistry, 1990
• Palladium-catalyzed formylation of organic halides with carbon monoxide and tin hydride
  Journal of the American Chemical Society, 1986
• Application of the Swern oxidation to the manipulation of highly reactive carbonyl compounds
  The Journal of Organic Chemistry, 1985
• The first practical method for asymmetric epoxidation
  Journal of the American Chemical Society, 1980
• TOTAL SYNTHESIS OF (±)-ANNONENE, A TRANS-CLERODANE DITERPENE
  Chemistry Letters, 1979
• Selective reductions. 22. Facile reduction of .alpha.,.beta.-unsaturated aldehydes and ketones with 9-borabicyclo[3.3.1]nonane. A remarkably convenient procedure for the selective conversion of conjugated aldehydes and ketones to the corresponding allylic alcohols in the presence of other functional groups
  The Journal of Organic Chemistry, 1977