High-pressure mediated Diels-Alder reaction of di-l-menthyl acetoxy-methylenemalonate with furan: Enantioselective synthesis of β-D-ribofuranosylmalonate, a prospective synthon for C-nucleoside

This publication has 7 references indexed in Scilit:

• Di-l-menthyl (acetoxymethylene)malonate, a new chiral dienophile: enantioselective route to carbocyclic analogs of C-nucleoside
  The Journal of Organic Chemistry, 1988
• Facile synthesis of the carbocyclic analogue of .BETA.-ribofuranosylmalonate, new synthon for carbocyclic C-nucleoside formation by retrograde aldol C-C bond fission.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
• Stereochemistry of diels-alder reaction at high pressure: asymmetric induction in the reaction of 1-methoxybuta-1,3-diene with sugar aldehydes
  Tetrahedron, 1986
• A Convenient Synthesis ofC-Glycofuranosylmalonates and Related Derivatives
  Synthesis, 1983
• Organic reactions at high pressure. Asymmetric induction in the diels-alder reaction of -benzoquinone with chiral 2,4-pentadienoic acid derivatives
  Tetrahedron Letters, 1982
• Stereochemistry of Diels-Alder Reactions at High Pressure. II. Influence of High Pressure on Asymmetric Induction in Condensation of (−)-Di-(R)-menthyl Fumarate with Butadiene and Isoprene
  Bulletin of the Chemical Society of Japan, 1979
• C-Glycosyl nucleosides. V. Unexpected observations on the relative stabilities of compounds containing fused five-membered rings with epimerizable substituents
  Journal of the American Chemical Society, 1975