Enantioselective addition of phenylacetylene to  N ‐aryl arylimines catalyzed by Cu(II)‐pyridine containing  N ‐tosylatedaminoimine ligand complex | Zendy

Liu Bao | Zendy; Zhong Yao | Zendy; Li Xingshu | Zendy

Premium

Enantioselective addition of phenylacetylene to N ‐aryl arylimines catalyzed by Cu(II)‐pyridine containing N ‐tosylatedaminoimine ligand complex

Author(s) -

Liu Bao,

Zhong Yao,

Li Xingshu

Publication year - 2009

Publication title -

chirality

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.43

H-Index - 77

eISSN - 1520-636X

pISSN - 0899-0042

DOI - 10.1002/chir.20649

Subject(s) - phenylacetylene , chemistry , enantioselective synthesis , pyridine , aryl , chirality (physics) , catalysis , ligand (biochemistry) , medicinal chemistry , stereochemistry , organic chemistry , receptor , biochemistry , alkyl , chiral symmetry breaking , physics , quantum mechanics , nambu–jona lasinio model , quark

Chiral tridentate N ‐tosylated pyridine‐containing ligands were prepared and used in the Cu(II)‐catalyzed enantioselective addition of phenylacetylene to N ‐aryl arylimines. Moderate to high enantioselectivities (up to 95% ee) were obtained in very mild reaction conditions. Chirality, 2008. © 2009 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research