Triphenyltin enolates, prepared from lithium enolates and triphenyltin chloride, undergo a rapid aldol condensation with aldehydes without the need for the presence of Lewis acids to give predominantly the erythro-product regardless of the geometry of the starting enolates.
Y. Yamamoto, H. Yatagai and K. Maruyama, J. Chem. Soc., Chem. Commun., 1981, 162 DOI: 10.1039/C39810000162
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