Chemical communications

Direct enantio-and diastereoselective Mannich reactions of malonate and β-keto esters with N-Boc and N-Cbz aldimines catalysed by a bifunctional cinchonine …

AL Tillman, J Ye, DJ Dixon

Index: Tillman, A. Louise; Ye, Jinxing; Dixon, Darren J. Chemical Communications, 2006 , # 11 p. 1191 - 1193

Full Text: HTML

Citation Number: 122

Abstract

A highly enantioselective Mannich reaction between malonate esters and N-Boc and N-Cbz aldimines, catalysed by a bifunctional cinchonine derivative, has been developed; extension of this methodology to encompass the use of 2-substituted-1, 3-dicarbonyl nucleophiles allows the formation of adjacent stereocentres, one of which is quaternary, in high relative and absolute stereocontrol.

Related Articles:

Enantioselective Aza??Henry Reactions Assisted by ZnII and N??Methylephedrine

[Palomo, Claudio; Oiarbide, Mikel; Halder, Rajkumar; Laso, Antonio; Lopez, Rosa Angewandte Chemie - International Edition, 2006 , vol. 45, # 1 p. 117 - 120]

Oxidative Mannich Reaction of N-Carbobenzyloxy Amines with 1, 3-Dicarbonyl Compounds

[Matsuo, Jun-Ichi; Tanaki, Yumi; Ishibashi, Hiroyuki Organic Letters, 2006 , vol. 8, # 19 p. 4371 - 4374]

Oxidative Mannich Reaction of N-Carbobenzyloxy Amines with 1, 3-Dicarbonyl Compounds

[Matsuo, Jun-Ichi; Tanaki, Yumi; Ishibashi, Hiroyuki Organic Letters, 2006 , vol. 8, # 19 p. 4371 - 4374]

Oxidative Mannich Reaction of N-Carbobenzyloxy Amines with 1, 3-Dicarbonyl Compounds

[Matsuo, Jun-Ichi; Tanaki, Yumi; Ishibashi, Hiroyuki Organic Letters, 2006 , vol. 8, # 19 p. 4371 - 4374]

Scope and limitations in sulfur ylide mediated catalytic asymmetric aziridination of imines: use of phenyldiazomethane, diazoesters and diazoacetamides

[Aggarwal; Ferrara; O'Brien; Thompson; Jones; Fieldhouse Journal of the Chemical Society. Perkin Transactions 1, 2001 , # 14 p. 1635 - 1643]

More Articles...