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1 series of copolymers with varying amount of fluorine substitution.
2 ss the generality of the effects produced by fluorine substitution.
3 ucture-activity relationships as a result of fluorine substitution.
4 luoromethanes also decreases with increasing fluorine substitution.
5 identical polymers, except for the number of fluorine substitutions (0, 1, or 2) on the repeat unit (
6 myl-gamma-glutamate to examine the effect of fluorine substitution adjacent to the scissile isopeptid
7 represent a valuable tool for designing new fluorine substitutions and support ligand optimization i
8 In the present investigation, the effect of fluorine substitution at aziridine positions other than
13 introduction of a benzyl alcohol group and a fluorine substitution, each of which resulted in over 10
15 ers, dependent on the number and site of the fluorine substitution: fluorine on carbon adjacent to th
18 ed cyclooctynes (OMe, Cl, F, CN) showed that fluorine substitution has the most dramatic effect on re
21 new N-heterocyclic carbene precursor bearing fluorine substitution in the backbone results in signifi
22 cts, our results suggest that the effects of fluorine substitution in the reactions of fluorinated ty
23 he conformational biases induced by a single fluorine substitution in the template can be enhanced by
24 cant structural perturbation imparted by the fluorine substitution in these complexes is a rotation o
26 We find that the stabilization imparted by fluorine substitution is additive over that obtained by
29 (X = H, F) as model systems, the effects of fluorine substitution on main-chain conformations, packi
30 synthesized in order to study the effects of fluorine substitution on monoamine oxidase inhibition.
31 our research program to study the effects of fluorine substitution on the biological activities of ne
37 dies of this class of antivirals showed that fluorine substitution on the left-hand phenyl ring in co
38 was used to gain insight into the impact of fluorine substitution on the overall protein structure a
42 -band gap conjugated molecules with specific fluorine substitution patterns has been synthesized in o
45 7% with PBnDT-DTffBT (2F) but also suggests fluorine substitution should be generally considered in
46 (cat)/K(M) = 30 M(1) s(1)) based on a single fluorine substitution that originates from differences i
51 ated a remarkable electronic effect of the 4-fluorine substitution, while the effect of the 4-methyl
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