Tetrahedron letters

Straightforward synthesis of α, β-epoxysilanes from terminal epoxides by lithium 2, 2, 6, 6-tetramethylpiperidide-mediated deprotonation-in situ silylation

DM Hodgson, NJ Reynolds, SJ Coote

Index: Hodgson, David M.; Reynolds, Nigel J.; Coote, Steven J. Tetrahedron Letters, 2002 , vol. 43, # 44 p. 7895 - 7897

Full Text: HTML

Citation Number: 22

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Lithiation-in situ silylation of simple terminal epoxides using lithium 2,2,6,6-tetramethylpiperidide in combination with trimethylsilyl chloride provides a direct and experimentally convenient process for the synthesis of trans-α,β-epoxysilanes. ... A study of the LTMP-mediated in situ ...

Related Articles:

Enantioselective Synthesis of (R)??Homoboroproline from (S)??Proline Using a Borylation Approach

[Georgiou, Irene; Whiting, Andrew European Journal of Organic Chemistry, 2012 , # 22 p. 4110 - 4113]

Stereoselective synthesis of N-protected pyrrolidines via Pd-catalyzed reactions of γ-(N-acylamino) alkenes and γ-(N-Boc-amino) alkenes with aryl bromides

[Bertrand, Myra Beaudoin; Wolfe, John P. Tetrahedron, 2005 , vol. 61, # 26 p. 6447 - 6459]

More Articles...