A mild and efficient method for the formation of allylstannanes utilizing SmI2-induced polarity inversion of π-allyl palladium complexes

This publication has 10 references indexed in Scilit:

• Diastereodivergent control in the reactions of allylic and allenic organometallic reagents with pyruvates
  The Journal of Organic Chemistry, 1986
• Palladium-catalyzed coupling of electrogenerated allyltin reagents
  Tetrahedron Letters, 1986
• Highly stereoselective reaction ofα-methylthio aldehydes with allyltriphenylstannane: Synthesis of anti-β-methylthio alcohols
  Tetrahedron Letters, 1985
• Synthesis of Homoallylic Alcohols from Allylic Phosphates and Aldehydes with Organoaluminum Reagent Containing Al–Sn Linkage
  Bulletin of the Chemical Society of Japan, 1985
• Stereocontrolled additions of allyltri-n-butyl-stannane to α-hydroxyaldehyde derivatives. A useful route to monoprotected erythro or threo diols.
  Tetrahedron Letters, 1984
• Reformatsky Type Reaction with New Aluminium Reagents Containing Al–Sn or Al–Pb Linkage
  Bulletin of the Chemical Society of Japan, 1984
• Inversion of the electronic reactivity of allyl acetates using an aluminum-tin reagent
  Journal of the American Chemical Society, 1984
• Regioselective stannylmetalation of acetylenes in the presence of transition-metal catalyst
  Tetrahedron Letters, 1984
• Reactions of (organostannyl)- and (organogermyl)lithium reagents with some (allylic) cyclohex-2-enyl chlorides
  The Journal of Organic Chemistry, 1982
• Divalent lanthanide derivatives in organic synthesis. 1. Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agents
  Journal of the American Chemical Society, 1980