N-Trialkylsilyl Bistrifluoromethanesulfonimides (R3SiNTf2) Are Powerful Catalysts for the Highly Efficient α-Amido Alkylation Reactions of Silicon-Based Nucleophiles-Reference-Cited by-同舟云学术

N-Trialkylsilyl Bistrifluoromethanesulfonimides (R3SiNTf2) Are Powerful Catalysts for the Highly Efficient α-Amido Alkylation Reactions of Silicon-Based Nucleophiles

Published:2005-10-20 Issue:23 Volume:7 Page:5335-5337
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Othman Raja Ben¹,Bousquet Till¹,Othman Mohamed¹,Dalla Vincent¹

Affiliation:

1. Unité de Recherche en Chimie Organique et Macromoléculaire, Faculté des Sciences et Techniques de l'Université du Havre, 25 rue Philippe Lebon, BP 540, 76058 Le Havre Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol052357j

Reference18 articles.

1. N-Trimethylsilyl-bis(trifluoromethanesulfonyl)imide: a better carbonyl activator than trimethylsilyl triflate

2. Trimethylsilyl Bis(trifluoromethanesulfonyl)amide as an Effective Catalyst for the Friedel-Crafts Alkylation Reaction

3. Trimethylsilyl bis(trifluoromethanesulfonyl)imide as a tolerant and environmentally benign Lewis acid catalyst of the Diels–Alder reaction

4. The search for tolerant Lewis acid catalysts.

5. Synthesis, structure and high catalytic activity in the Diels–Alder reaction of ytterbium(III) and yttrium(III) bis(trifluoromethanesulfonyl)amide complexes

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