Reductive lithiation of methyl substituted diarylmethylsilanes: application to silanediol peptide precursors

D Hernandez, R Mose, T Skrydstrup

Index: Hernandez, Dacil; Mose, Rasmus; Skrydstrup, Troels Organic Letters, 2011 , vol. 13, # 4 p. 732 - 735

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Citation Number: 12

Abstract

Reductive lithiation of methyl-substituted diarylmethylsilanes using lithium naphthalenide represents a practical method for the preparation of the corresponding silyl lithium reagents. Their addition to chiral sulfinimines affords versatile precursors to silanols and silanediols. The replacement of the currently used diphenylsilane motif by a more labile diarylsilane moiety allows the selective hydrolysis of one or two aryl groups by treatment with TFA.