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1 iral, raising the possibility to use them as asymmetric catalysts.
2 dominant platform for hydrogen bond promoted asymmetric catalysts.
3 gained tremendous attention in the design of asymmetric catalysts.
4 drug discovery as well as from developers of asymmetric catalysts.
5  and predictive tool in the discovery of new asymmetric catalysts.
6 ngful predictions for the rational design of asymmetric catalysts.
7 = 1/3/3) are among the most enantioselective asymmetric catalysts across a broad range of mechanistic
8                       These preactivated GTM asymmetric catalysts act similarly to enzymes by control
9 metal complexes are among the most versatile asymmetric catalysts and have found utility in fields ra
10 design of everything from pharmaceuticals to asymmetric catalysts and organic materials.
11 tially useful in the combinatorial search of asymmetric catalysts and reagents.
12                    Tartaric acid is an ideal asymmetric catalyst as it is abundant, cheap, and enviro
13 cently have been used to guide the design of asymmetric catalysts, but their usage in dynamic covalen
14 nal chirally amplified helices as switchable asymmetric catalysts, chiral sensors, and circularly pol
15  using a three-dimensional model approach to asymmetric catalyst development.
16 pplications in high-throughput screening for asymmetric-catalyst discovery.
17 te the potential of these phosphopeptides as asymmetric catalysts, enantioselective transfer hydrogen
18 pyridylalanine (Pal) residue as an efficient asymmetric catalyst for enantioselective coupling reacti
19 sulting materials proved to be highly active asymmetric catalysts for diethylzinc and alkynylzinc add
20                          The optimization of asymmetric catalysts for enantioselective synthesis has
21 f particular note is the efficiency of these asymmetric catalysts for reactions involving challenging
22                                    Design of asymmetric catalysts generally involves time- and resour
23          The use of imidazolidinone 1 as the asymmetric catalyst has been found to mediate the fluori
24  pseudo-D3-symmetric knot was employed as an asymmetric catalyst in Mukaiyama aldol reactions, genera
25 traditional fields of chirality, such as the asymmetric catalysts in the molecular world and the chir
26 scaffolds should contribute to the design of asymmetric catalysts operating with low amounts of chira
27   A data-descriptive classification of these asymmetric catalysts reveals an increasingly broad set o
28 ed substrates to illustrate unequivocally an asymmetric catalyst-substrate binding event.
29  = lanthanide(III)] are exceptionally useful asymmetric catalysts that exhibit high levels of enantio
30  A metal-coordination-based high performance asymmetric catalyst utilizing metal centrochirality as t
31                                In this work, asymmetric catalyst was prepared by encapsulating metall
32                     A series of 19 different asymmetric catalysts were screened in an effort to ident
33 x featuring an aldehyde group as a versatile asymmetric catalyst with remarkably broad scope.
34 eolite catalysts have recently proved useful asymmetric catalysts, with chirality emerging from their