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1 C condensins are not required to compact DNA chirally.
2 elopment of this class of catalysts built on chirally amplified helical scaffolds should contribute t
3        However, the nature of the underlying chirally asymmetric cytoskeletal processes has remained
4 ties of the adult human heart, with sinuous, chirally asymmetric paths of flow through the whole.
5  the inference from earlier experiments with chirally deuterated FPP.
6                                 In addition, chirally deuterated tunicamycins produced by fermentatio
7 r evolution of D-ribose RNA and probably was chirally directed by the orientation of early RNA molecu
8 teractions are important in the formation of chirally directed clusters.
9              We now report evidence that two chirally distinct forms of SSHR composed of all l or all
10 R(P) chirality at every other position (R(P) chirally enriched MPOs) or (ii) alternating R(P) MP/phos
11 rine under relatively mild conditions yields chirally enriched serine octamers and that the chiral pr
12 here is direct evidence for nanometer scale, chirally induced organization into specific structures.
13 is indicated by the observation that COMC-6 (chirally labeled with deuterium at the exomethylene carb
14                               It relies on a chirally modified aryliodine(I) catalyst and proceeds wi
15 from research on asymmetric hydrogenation on chirally modified noble metals will be presented.
16 n of such catalysts will be elucidated using chirally modified platinum catalysts for the asymmetric
17                                              Chirally modified Pt catalysts are used in the heterogen
18 ylene oxide is measured on a Pd(111) surface chirally modified using (S)- and (R)-2-butanol.
19                         The amplification of chirally modified, non-linear signals from quantum emitt
20 amide, with a mainly protonated backbone and chirally mounted imidazolylmethylene side chains that ar
21 31 ASOs were prepared with control of the PS chirally of each linkage within the gap in an attempt to
22 rring L-amino acids, it is favorable for the chirally opposite D-amino acids.
23 ghly luminescent achiral chromophores and/or chirally perturbing moieties), as well as for the improv
24                   The new design is based on chirally perturbing the acting achiral chromophore by or
25 cids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptides, and
26  yields of 4'-thioribonucleosides by using a chirally pure (R)-sulfoxide precursor.
27 l)- and -dipeptidoylbenzotriazoles to afford chirally pure 1,3,4-thiadiazol-2-yl-substituted amino ac
28                                              Chirally pure dimer synthons were also prepared with 2'-
29       Unfortunately, the development of some chirally pure drug molecules is hampered by rapid in viv
30 imethyl analogue trans-1b, was resolved into chirally pure enantiomers.
31                                              Chirally pure methylphosphonate deoxyribooligonucleotide
32                 However, the introduction of chirally pure methylphosphonate groups shows that the ef
33 presentative series 4a-i was prepared as the chirally pure R(+) enantiomers, and from these, the 4-ch
34 evelopment of methods for the preparation of chirally pure solids, in particular where the building b
35        Our analysis shows that this use of a chirally resolved valyl phosphonate results in selection
36 chaean earth's anoxic atmosphere followed by chirally selective damage of biomolecules due to circula
37 his is the first case in which assemblies of chirally selective elongated structures are observed in
38 g of the enantiomeric pair to DNA is clearly chirally selective, and each of the enantiomers was foun
39 ers to exhibit "magic" numbers, which can be chirally selective, these experiments provide a rigorous
40                                              Chirally sensitive measurement techniques have generally
41 and emitters occupy this light-confining and chirally sensitive region.
42 udy the effects of natural organic matter on chirally separated SWNT aggregation.
43                              The reaction is chirally specific in that any one enzyme usually only re
44 brane phospholipid bilayer without involving chirally specific receptor/transporter mechanisms.
45 hol side product and the racemization of the chirally unstable alpha-substituted aldehyde intermediat

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