Copper-catalyzed alkene diamination: synthesis of chiral 2-aminomethyl indolines and pyrrolidines-Reference-Cited by-同舟云学术

Copper-catalyzed alkene diamination: synthesis of chiral 2-aminomethyl indolines and pyrrolidines

Published:2014 Issue:5 Volume:5 Page:1786-1793
ISSN:2041-6520
Container-title:Chem. Sci.
language:en
Short-container-title:Chem. Sci.

Author:

Turnpenny Benjamin W.¹²³⁴,Chemler Sherry R.¹²³⁴

Affiliation:

1. Department of Chemistry

2. Natural Science Complex

3. The State University of New York at Buffalo

4. Buffalo, USA

Abstract

Enantioselective copper-catalyzed alkene diamination provides chiral 2-aminomethyl indolines and pyrrolidines via oxidative coupling of primary sulfonamides with N-sulfonyl-2-allylanilines and N-sulfonyl-4-pentenamines.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/SC/C4SC00237G

Reference35 articles.

1. Catalytic asymmetric borane reduction of prochiral ketones by the use of diazaborolidine catalysts prepared from chiral β-diamines

2. Copper-Catalyzed Enantioselective Henry Reaction of Enals and Subsequent Iodocyclization: Stereoselective Construction of Chiral Azatricyclic Frameworks

3. Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes

4. Catalytic Direct Asymmetric Michael Reactions: Taming Naked Aldehyde Donors

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