Indium trichloride-promoted tin-mediated carbonyl allylation in water: High simple diastereo- and diastereofacial selectivity

This publication has 24 references indexed in Scilit:

• Chelation control associated with organometallic addition reactions in water. The high stereoselectivity offered by α- and β-hydroxyl substituents obviates the need for protecting groups
  Tetrahedron Letters, 1995
• Synthesis of anti-Homoallylic Alcohols and Monoprotected 1,2-Diols through InCl3-Promoted Addition of Allylic Stannanes to Aldehydes
  The Journal of Organic Chemistry, 1995
• Tin- and indium-mediated allylation in aqueous media: application to unprotected carbohydrates
  The Journal of Organic Chemistry, 1993
• Organic reactions in aqueous media - with a focus on carbon-carbon bond formation
  Chemical Reviews, 1993
• Palladium-catalyzed carbonyl allylation by allylic alcohols with stannous chloride
  Journal of the American Chemical Society, 1992
• Reaction of Propargyl Bromide with Aldehydes in the Presence of Metallic Tin. Synthesis of Homopropargylalcohols and Homoallenylalcohols
  Synthetic Communications, 1990
• Synthesis of homoallylic alcohols in aqueous media
  The Journal of Organic Chemistry, 1989
• Indium in organic synthesis: indium-mediated allylation of carbonyl compounds
  The Journal of Organic Chemistry, 1988
• Allylzinc reagents additions in aqueous media
  The Journal of Organic Chemistry, 1985
• Allylation of aldehydes and ketones in the presence of water by allylic bromides, metallic tin, and aluminum
  Organometallics, 1983