New camphor derived chiral ligands for asymmetric synthesis

1998 ◽  
Vol 9 (22) ◽  
pp. 4009-4020 ◽  
Author(s):  
Max Knollmüller ◽  
Mathias Ferencic ◽  
Peter Gärtner ◽  
Kurt Mereiter ◽  
Christian R. Noe
Synlett ◽  
2021 ◽  
Author(s):  
Dongxu Yang ◽  
Linqing Wang

AbstractMagnesium (Mg) is a cheap, non-toxic, and recyclable alkaline earth metal that constitutes about 2% weight in the Earth’s crust. The use of magnesium catalysts to forge chiral moieties in molecules is highly attractive. Based on our work in recent years, we describe the current progress in the development of in situ generated magnesium catalysts and their application in asymmetric synthesis. In this perspective, a critically concise classification of in situ generated magnesium catalytic modes, with relevant examples, is presented, and representative mechanisms of each category are discussed. Building on the established diverse strategies, one can foresee that more innovative and structurally creative magnesium catalysts that are generated in situ will be developed to overcome more formidable challenges of catalytic enantioselective reactions.1 Introduction2 Magnesium Catalysts Generated in Situ from Chiral Ligands Containing Dual Reactive Hydrogens3 Magnesium Catalysts Generated in Situ from Monoanionic Chiral Ligands4 Bimetallic and Polymetallic Magnesium Catalysts Assembled in Situ5 Summary and Outlook


2003 ◽  
Vol 68 (5) ◽  
pp. 885-898 ◽  
Author(s):  
Brian Pedersen ◽  
Tobias Rein ◽  
Inger Søtofte ◽  
Per-Ola Norrby ◽  
David Tanner

Some new results on asymmetric synthesis via the addition of α-metalated methyl tolyl sulfoxides to imines are presented. Good diastereoselectivity (up to >98% d.e. for product 3g) can be obtained under conditions of kinetic control (short reaction time, low temperature). The transition state (a six-membered "flat chair") was probed by quantum mechanical calculations, which underpinned the idea of using external chiral ligands to enhance the diastereoselectivity of otherwise moderately selective reactions. In this way, the diastereomeric ratio of the product 3a could be raised from (84:16) to (>99:1) by use of a readily available C2-symmetric bis(sulfonamide) ligand.


2014 ◽  
Vol 86 (3) ◽  
pp. 273-281 ◽  
Author(s):  
Corinne Aubert ◽  
Marion Barbazanges ◽  
Anny Jutand ◽  
Sara H. Kyne ◽  
Cyril Ollivier ◽  
...  

AbstractTwo organometallic catalysis studies are presented. The first one deals with the development of a new catalytic agent based on the mixture of a hydride and an iron salt to trigger efficient radical cyclization processes. In a second line of research, we have shown that the use of chiral anions can outperform chiral ligands in a carbocyclization reaction and a [2 + 2 + 2] cycloaddition.


ChemInform ◽  
2010 ◽  
Vol 30 (18) ◽  
pp. no-no
Author(s):  
Max Knollmueller ◽  
Mathias Ferencic ◽  
Peter Gaertner ◽  
Kurt Mereiter ◽  
Christian R. Noe

Synthesis ◽  
1990 ◽  
Vol 1990 (07) ◽  
pp. 541-549 ◽  
Author(s):  
Kiyoshi Tomioka

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