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Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines: dual stereocontrol with nearly perfect diastereoselectivity†
Qiang Liu,Ping Tian,Jing-Chao Tao,Guo-Qiang Lin
Organic & Biomolecular Chemistry Pub Date : 03/02/2015 00:00:00 , DOI:10.1039/C5OB00322A
Abstract

Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines has been described. Dual stereocontrol, through the combination of a chiral auxiliary and a chiral copper complex, has played an important role in achieving the nearly perfect diastereoselectivities (all dr > 99 : 1), especially for ketimine substrates.

Graphical abstract: Copper-catalyzed asymmetric allylation of chiral N-tert-butanesulfinyl imines: dual stereocontrol with nearly perfect diastereoselectivity
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