Silylium-Catalyzed Regio- and Stereoselective Carbosilylation of Ynamides with Allylic Trimethylsilanes
Силилиево-катализируемое региоселективное и стереоселективное карбосилилирование инамидов аллильными триметилсиланами
2023-02-07
SCID: 54.1/f74exvk2
Discuss with AI
allylic trimethylsilanesregioselective carbosilylationsilylium catalysisstereoselective carbosilylationynamides
Figures from the paper
Abstract (AI)
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.
Key Findings
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.
Research Object
tosylynamides reacting with allylic trimethylsilanes under silylium catalysis
Research Subject
regio- and stereoselective carbosilylation, including C–C triple-bond activation and formation of (Z)-α-allyl-β-trimethylsilylenamides
Publication Details
Publication Date
2023-02-07
Journal
Publisher
ISSN
Cited by
13
Open access PDF
Access Type
Author Information
Download PDF
Subscribe to digest