Expanding the Forefront of Strong Organic Brønsted Acids: Proton-Catalyzed Hydroamination of Unactivated Alkenes and Activation of Au(I) for Alkyne Hydroamination-Reference-Cited by-同舟云学术

Expanding the Forefront of Strong Organic Brønsted Acids: Proton-Catalyzed Hydroamination of Unactivated Alkenes and Activation of Au(I) for Alkyne Hydroamination

Published:2015-04-08 Issue:8 Volume:17 Page:1930-1933
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mirabdolbaghi Roya¹,Dudding Travis¹

Affiliation:

1. Department of Chemistry, Brock University, 500 Glenridge Avenue, St. Catharines, Ontario L2S 3A1, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00617

Reference27 articles.

1. Modulating the Acidity: Highly Acidic Brønsted Acids in Asymmetric Catalysis

2. New reaction and new catalyst—a personal perspective

3. Polystyrene-Bound Tetrafluorophenylbis(triflyl)methane as an Organic-Solvent-Swellable and Strong Brønsted Acid Catalyst The authors thank Mr. Shoichi Kondo for the single-crystal X-ray analysis. Sodium triflate was generously donated by Central Glass Co., Ltd., Japan. The authors also acknowledge Dr. Yuko Wasada and Dr. Manabu Kubota for their helpful discussions on the theoretical calculations.

4. Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Brønsted Acid and Its Application to Asymmetric Diels−Alder Reaction

5. A Brønsted Acid Catalyst for the Enantioselective Protonation Reaction

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