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1 and predictive tool in the discovery of new asymmetric catalysts.
2 dominant platform for hydrogen bond promoted asymmetric catalysts.
3 ngful predictions for the rational design of asymmetric catalysts.
4 iral, raising the possibility to use them as asymmetric catalysts.
5 = 1/3/3) are among the most enantioselective asymmetric catalysts across a broad range of mechanistic
8 cently have been used to guide the design of asymmetric catalysts, but their usage in dynamic covalen
11 te the potential of these phosphopeptides as asymmetric catalysts, enantioselective transfer hydrogen
12 pyridylalanine (Pal) residue as an efficient asymmetric catalyst for enantioselective coupling reacti
13 sulting materials proved to be highly active asymmetric catalysts for diethylzinc and alkynylzinc add
15 f particular note is the efficiency of these asymmetric catalysts for reactions involving challenging
17 pseudo-D3-symmetric knot was employed as an asymmetric catalyst in Mukaiyama aldol reactions, genera
18 traditional fields of chirality, such as the asymmetric catalysts in the molecular world and the chir
19 scaffolds should contribute to the design of asymmetric catalysts operating with low amounts of chira
21 = lanthanide(III)] are exceptionally useful asymmetric catalysts that exhibit high levels of enantio
22 A metal-coordination-based high performance asymmetric catalyst utilizing metal centrochirality as t
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