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1 series of copolymers with varying amount of fluorine substitution.
2 ation are strengthened with increasing ortho fluorine substitution.
3 ss the generality of the effects produced by fluorine substitution.
4 ucture-activity relationships as a result of fluorine substitution.
5 luoromethanes also decreases with increasing fluorine substitution.
6 f varying sizes and shapes, with and without fluorine substitutions.
7 identical polymers, except for the number of fluorine substitutions (0, 1, or 2) on the repeat unit (
8 myl-gamma-glutamate to examine the effect of fluorine substitution adjacent to the scissile isopeptid
11 40 angstrom to 1.26 angstrom with increasing fluorine substitution and increasing s-character of the
12 represent a valuable tool for designing new fluorine substitutions and support ligand optimization i
13 In the present investigation, the effect of fluorine substitution at aziridine positions other than
16 strategic structural modifications, such as fluorine substitution at the bridgehead sp(3) carbon or
20 introduction of a benzyl alcohol group and a fluorine substitution, each of which resulted in over 10
23 ers, dependent on the number and site of the fluorine substitution: fluorine on carbon adjacent to th
27 ed cyclooctynes (OMe, Cl, F, CN) showed that fluorine substitution has the most dramatic effect on re
30 new N-heterocyclic carbene precursor bearing fluorine substitution in the backbone results in signifi
31 cts, our results suggest that the effects of fluorine substitution in the reactions of fluorinated ty
32 he conformational biases induced by a single fluorine substitution in the template can be enhanced by
33 cant structural perturbation imparted by the fluorine substitution in these complexes is a rotation o
36 We find that the stabilization imparted by fluorine substitution is additive over that obtained by
39 (X = H, F) as model systems, the effects of fluorine substitution on main-chain conformations, packi
40 synthesized in order to study the effects of fluorine substitution on monoamine oxidase inhibition.
41 our research program to study the effects of fluorine substitution on the biological activities of ne
47 dies of this class of antivirals showed that fluorine substitution on the left-hand phenyl ring in co
48 was used to gain insight into the impact of fluorine substitution on the overall protein structure a
50 Unlike earlier PIs, these compounds have fluorine substitutions on the P2-P4 macrocycle and P1 mo
53 -band gap conjugated molecules with specific fluorine substitution patterns has been synthesized in o
56 7% with PBnDT-DTffBT (2F) but also suggests fluorine substitution should be generally considered in
57 (cat)/K(M) = 30 M(1) s(1)) based on a single fluorine substitution that originates from differences i
59 o systematically analyze the contribution of fluorine substitutions to inhibitor potency and resistan
64 ated a remarkable electronic effect of the 4-fluorine substitution, while the effect of the 4-methyl