Silylium-Catalyzed Regio- and Stereoselective Carbosilylation of Ynamides with Allylic Trimethylsilanes

Силилиево-катализируемое региоселективное и стереоселективное карбосилилирование инамидов аллильными триметилсиланами
Paz Yepes, A.L. Suarez-Sobrino, Miguel A. Rodrı́guez, Alfredo Ballesteros
2023-02-07

allylic trimethylsilanesregioselective carbosilylationsilylium catalysisstereoselective carbosilylationynamides
High Resolution Image Download MS PowerPoint Slide The regio- and stereoselective carbosilylation of tosylynamides with allylic trimethylsilanes takes place under mild conditions in the presence of catalytic TMSNTf 2 or HNTf 2 to give ( Z )-α-allyl-β-trimethylsilylenamides with good yields. Theoretical calculations show the activation of the C–C triple bond of the ynamides by the trimethylsilylium ion and formation of a β-trimethylsilylketenimonium cation. Further transformations of the products demonstrate the synthetic utility of this reaction.
1
Catalytic TMSNTf₂ or HNTf₂ affords (Z)-α-allyl-β-trimethylsilylenamides in good yields.
2
Further transformations of the carbosilylation products demonstrate their synthetic utility.
3
The reaction proceeds through trimethylsilylium-ion activation of the ynamide C–C triple bond and formation of a β-trimethylsilylketenimonium cation.
4
Tosylynamides undergo regio- and stereoselective carbosilylation with allylic trimethylsilanes under mild catalytic conditions.

tosylynamides reacting with allylic trimethylsilanes under silylium catalysis

regio- and stereoselective carbosilylation, including C–C triple-bond activation and formation of (Z)-α-allyl-β-trimethylsilylenamides

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2023-02-07
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Authors
Paz Yepes
A.L. Suarez-Sobrino
Miguel A. Rodrı́guez
Alfredo Ballesteros
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