Aldol reaction of 4-trimethylsiloxy-6-methylene-1,3-dioxines with chiral aldehydes: Enantioselective synthesis of 1,3-dioxin-4-ones having a 2,3-dihydroxylated alkyl group at the 6-position

This publication has 17 references indexed in Scilit:

• Two lactone formation reactions from 1,3-dioxin-4-ones having hydroxyalkyl group at the 6-position: Difference in ring opening and closure
  Tetrahedron, 1991
• The formal oxidative addition of electron-rich transoid dienes to bromonaphthoquinones
  The Journal of Organic Chemistry, 1991
• Synthesis of 1,3-dioxin-4-ones and their use in synthesis. Part XXIV. A novel synthesis of .BETA.-ketothioesters.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1990
• 1,3‐dioxin‐4‐ones as versatile intermediates for organic synthesis
  Journal of Heterocyclic Chemistry, 1990
• Enantiomerically Pure 2-(Carbamoyloxy)oxiranes and Their Utility in the Synthesis of D- and L-3,6-Dideoxy-3-C-methylhexofuranosides via the Homoaldol Reaction
  Synthesis, 1989
• 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranes
  Tetrahedron Letters, 1987
• Acyclic stereoselection. 36. Simple diastereoselection in the Lewis acid mediated reactions of enol silanes with aldehydes
  The Journal of Organic Chemistry, 1986
• Lewis acid mediated aldol condensations using thioester silyl ketene acetals
  Tetrahedron, 1986
• Aldol-additions t0eα- and β-alkoxy aldehydes: The effect of chelation on simple diastereoselectivity
  Tetrahedron, 1984
• Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelates
  Tetrahedron, 1984