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1  interact with two adsorbates to catalyze an asymmetric reaction.
2  the sample of valine of unknown ee from the asymmetric reaction.
3 (S)-2 were used to screen catalysts for this asymmetric reaction.
4 y mild Lewis acid catalysts to provide novel asymmetric reactions.
5 pockets to mimic natural enzymes and promote asymmetric reactions.
6 activate adjacent functionality in catalytic asymmetric reactions.
7 ea of general concepts and widely applicable asymmetric reactions.
8 nd predicting the roles of such catalysts in asymmetric reactions.
9 n good yields in most cases and high % ee in asymmetric reactions.
10 e enantiopure forms and are directly used in asymmetric reactions.
11 valuable methodologies to a broader range of asymmetric reactions.
12  latter derives from the chiral pool and two asymmetric reactions-a ketone reduction using CBS-oxazab
13 stereocentres in a single reaction, multiple asymmetric reactions also impart increased enantiomeric
14  are further verified by chromatography-free asymmetric reaction analysis with small aliquots of crud
15 c cyclic allene intermediates in a catalytic asymmetric reaction and provide evidence for two distinc
16 tility of this method to further model other asymmetric reactions and facilitate the discovery proces
17 rk will enable extension of copper-catalyzed asymmetric reactions and provide understanding on how to
18 n of the stereochemical outcome of catalytic asymmetric reactions and second, achiral chromatography
19 work has expanded the scope of MOF-catalyzed asymmetric reactions and showed that the mixed linker st
20 rease in interest toward efficient catalytic asymmetric reactions and the rapid growth in the field o
21 ngs suggest that by fundamentally taming the asymmetric reactions, aqueous batteries are viable tools
22                   Transition metal-catalyzed asymmetric reactions are of high contemporary importance
23 effects of fluorine atom(s) on the course of asymmetric reactions are outlined in this tutorial revie
24                                    Catalytic asymmetric reactions are primarily used to install new s
25            In contrast, we have optimized an asymmetric reaction by modification of a series of achir
26 t could open up new venues in the control of asymmetric reactions by means of achiral appended polyme
27 ated that by controlling the SAM properties, asymmetric reactions can be catalyzed by Au clusters emb
28             The development of new catalytic asymmetric reactions can lead to exciting new strategies
29                        The products of these asymmetric reactions can serve as precursors to a number
30  results pave the way towards new studies on asymmetric reactions catalyzed in confined achiral cavit
31 es is a problem of fundamental importance in asymmetric reaction design, especially given that only a
32        This synopsis will address catalytic, asymmetric reactions developed to synthesize pyrroloindo
33                           Catalyst design in asymmetric reaction development has traditionally been d
34 screening applications including streamlined asymmetric reaction development.
35 hemical model has impeded the development of asymmetric reactions employing a lone chiral catalyst, i
36 are potentially useful for rapid analysis of asymmetric reactions for amino acid synthesis as well as
37                                        These asymmetric reactions from voters and donors may provide
38 ansformation; this is the first time that an asymmetric reaction has been discovered solely on the ba
39             The high synthetic value of this asymmetric reaction has been proven by the formal synthe
40           Many examples of peptide-catalyzed asymmetric reactions have appeared in the literature sin
41                   Transition-metal-catalyzed asymmetric reactions have been a powerful tool in organi
42 cent years, however, an increasing number of asymmetric reactions have been documented where this rel
43                                              Asymmetric reactions in water and in aqueous solutions h
44                                     However, asymmetric reactions in which both substrate and product
45 nd potentially provides the first view of an asymmetric reaction intermediate.
46                        The rhodium-catalyzed asymmetric reaction involving a terminal acetylene was d
47  foundation for the development of catalytic asymmetric reactions involving these classically avoided
48 urse and stereoselectivity of many catalytic asymmetric reactions is an important area of interest fo
49 that is especially suitable for the study of asymmetric reactions is presented.
50 ne current bottleneck in these approaches to asymmetric reactions is the determination of ee, which h
51  3(DMEDA) 3(BINOLate) 3La in three catalytic asymmetric reactions led to enantioselectivities similar
52 ted with an amino alcohol generated from the asymmetric reaction of a meso-epoxide with an alkyl amin
53               This compound can catalyze the asymmetric reaction of alkyl and aryl alkynes with N-(di
54  and Ti(O(i)Pr)(4) were used to catalyze the asymmetric reaction of alkynes with aldehydes to generat
55 nism, is an efficient organocatalyst for the asymmetric reaction of homophthalic anhydride with imine
56 nexpected diastereoselectivity in the double asymmetric reaction of N-acetyl-d-alaninal 1 and the tar
57 eveloped dialkylzinc addition, the catalytic asymmetric reactions of aryl-, vinyl-, and alkynylzinc r
58 de a comprehensive treatise on the catalytic asymmetric reactions of deconjugated butenolides reporte
59 spite their significant potential, catalytic asymmetric reactions of olefins with formaldehyde are ra
60 nocatalytic modalities resulted in divergent asymmetric reaction patterns to furnish angularly fused
61                        We report a catalytic asymmetric reaction process that involves the use of sol
62 e structural assignment, particularly during asymmetric reaction processes.
63 xcess (e.e./d.e.) and product yield of crude asymmetric reaction products.
64 ing relations that explain, for example, the asymmetric reaction profiles observed for systems bound
65                                          The asymmetric reaction resulted in chiral N-phosphonyl amin
66 s have spurred the development of intriguing asymmetric reaction strategies during the last decade.
67 try represents a rare example of a catalytic asymmetric reaction that is highly enantioselective unde
68                                              Asymmetric reactions that convert racemic mixtures into
69         We present some selected examples of asymmetric reactions that involve fluorinated components
70 ine of unknown ee was synthesized through an asymmetric reaction to produce a realistic reaction samp
71 tion of chiral p-block element catalysts for asymmetric reactions to generate value-added compounds.
72              Achieving dual stereocontrol in asymmetric reactions using a single enantiomer for the b
73   Chiral supporting electrolytes can mediate asymmetric reactions via direct electrolysis, but their
74                             Additionally, an asymmetric reaction was developed to provide enantioenri
75 d achieving up to >99:1 dr selectivity, this asymmetric reaction was successfully applied to produce
76 mbient temperature, although the ee's of the asymmetric reactions were reduced in these examples.
77                        The products of these asymmetric reactions were shown to be readily converted
78 action media as well as chiral catalysts for asymmetric reactions, which are presently being investig
79 nables the use of functional alkynes in this asymmetric reaction with excellent enantioselectivity.
80  under a minute, enabling its use for HTS of asymmetric reactions with acceptable accuracy.
81                      Additionally, the first asymmetric reactions with Co(III) -catalyzed C-H functio