The cerium (III) mediated reaction of trimethylsilylmethyl magnesium chloride with esters and lactones: The efficient synthesis of some functionalised allylsilanes of use in annulation reactions

This publication has 12 references indexed in Scilit:

• Bifunctional annulating reagents: The use of novel allylsilanes for the one-pot preparation of six and seven-membered rings
  Tetrahedron Letters, 1988
• Characteristics in the reactions of allylsilanes and their applications to versatile synthetic equivalents
  Accounts of Chemical Research, 1988
• The preparation and reactions with an o-silylated enolate of an allylsilane bifunctional [3 + 2] annulating reagent
  Tetrahedron, 1988
• Direct access to functionalised allylsilanes: The cerium(III) mediated grignard reaction of functionalised esters and lactones.
  Tetrahedron Letters, 1988
• The cerium mediated conversion of esters to allylsilanes
  Tetrahedron Letters, 1987
• Novel annulation reactions: A simple preparation of spirocycles and an allylsilane based bifunctional acceptor-donor annulating reagent
  Tetrahedron Letters, 1986
• OZONOLYTIC CLEAVAGE OF CYCLOHEXENE TO TERMINALLY DIFFERENTIATED PRODUCTS: METHYL 6-OXOHEXANOATE, 6,6-DIMETHOXYHEXANAL, METHYL 6,6-DIMETHOXYHEXANOATE
  Organic Syntheses, 1986
• Cerium chloride-promoted nucleophilic addition of grignard reagents to ketones an efficient method for the synthesis of tertiary alcohols
  Tetrahedron Letters, 1985
• Termination of biomimetic cyclizations by the allylsilane function. Formation of the steroid nucleus in one step from an acyclic polyenic chain
  Journal of the American Chemical Society, 1983
• Ozonolytic cleavage of cycloalkenes to terminally differentiated products
  Tetrahedron Letters, 1982