Issue 5, 2014

Highly enantioselective oxidative tandem cyclization reaction: a chiral ligand and an anion cooperatively control stereoselectivity

Abstract

The unprecedented combination of a palladium(II) complex with a chiral Bu-QUOX ligand and a chiral phosphoric acid enables the highly efficient asymmetric oxidative tandem cyclization of N-(2,2-disubstituted hex-5-en-1-yl)acrylamides, providing a straightforward method to access chiral 6,5-bicyclic aza-heterocycles in moderate to good yields and with excellent enantioselectivities.

Graphical abstract: Highly enantioselective oxidative tandem cyclization reaction: a chiral ligand and an anion cooperatively control stereoselectivity

Supplementary files

Article information

Article type
Research Article
Submitted
15 Feb 2014
Accepted
24 Mar 2014
First published
25 Mar 2014

Org. Chem. Front., 2014,1, 473-476

Author version available

Highly enantioselective oxidative tandem cyclization reaction: a chiral ligand and an anion cooperatively control stereoselectivity

Y. He, H. Wu, L. Xu, Y. Su and L. Gong, Org. Chem. Front., 2014, 1, 473 DOI: 10.1039/C4QO00042K

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