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1  meso substituents of a controlled degree of bulkiness.
2 nhanced with a decrease in the ligand's para-bulkiness.
3 vide continuous measurements owing to device bulkiness(5-11), and existing wearable cardiac devices c
4 owed low sensory quality, mainly due to high bulkiness and adhesiveness.
5                     Thus, reducing sidechain bulkiness and expanding surface loops results in increas
6  maintaining minimal perturbations in steric bulkiness and overall polarity of the triphosphate polya
7 icity, hydrophilicity, volume, surface area, bulkiness and refractivity.
8                                   The steric bulkiness and rich chemical functionality of riboflavin
9 on has not been developed yet because of the bulkiness and rigidity of conventional imaging modules a
10 ed by current technologies because of device bulkiness and rigidity.
11                                The 2-Se atom bulkiness and the electronic effect are probably the mai
12                    The results show that the bulkiness and the reactivity of this doubly activated in
13 by various limitations such as inefficiency, bulkiness, and complexity.
14 eals a complex interplay between the charge, bulkiness, and location of amino acid residues in confer
15  such as substrate conformation, nucleophile bulkiness, and remote steric features can affect stereos
16 uent, stable interactions with RXRalpha, and bulkiness at C4 increased steric complementarity with th
17 omatic thiolate ligands (-SR) with different bulkiness at the para-position are synthesized and inves
18 y inert alkyl chains of different length and bulkiness, attached to in-plane N atoms of nearly orthog
19 ogical processes by altering an amino acid's bulkiness, charge, and hydrogen bonding interactions.
20                        We examine how remote bulkiness, electronic groups, and expanded-ring NHCs (ER
21                                     Enhanced bulkiness enhances the nucleophilic Cu-H moiety.
22 nic interactions (n --> pi*) and side chains bulkiness in promoting cis-amides was essentially invest
23 ketone peptide analogues with varying steric bulkiness in the P1 position and tested the ability of t
24 ts ranging from 172.2 to 325.44 Da; positive bulkiness index and hydrophobicity (except PP and PY) an
25 e supramolecular receptor not only with the "bulkiness" necessary for the NMR chemosensing approach b
26 n loss of PARG inhibition and the length and bulkiness of 8-adenosyl substituents was shown.
27 lored the possibility that by increasing the bulkiness of acrolein-adducted proteins, adduct-trapping
28                                          The bulkiness of amino acid residues in the C-terminal third
29 orded different products which depend on the bulkiness of aryl substituents.
30 PLM partially suffers from the high-cost and bulkiness of conventional lens-based microscopy, and its
31 de high sensitivity and specificity, but the bulkiness of experimental instruments and complicated pr
32 ycled large-volume commodity plastics due to bulkiness of foam products and associated contaminants.
33 dues this coupling is fostered by decreasing bulkiness of hydrophobic side chains due to larger hydra
34 h more sensitive toward the increased steric bulkiness of inhibitors compared to influenza A neuramin
35 selectivity of foldamers originates from the bulkiness of oligomers with four or more subunits, which
36 nto the K+ channel Kv1.4, and found that the bulkiness of residues in the inactivation peptide is ess
37 phenols were investigated in relation to the bulkiness of substituents at the 2 and 6 positions of th
38 tivity decreases with increase in the steric bulkiness of the adducts.
39  interactions become less important when the bulkiness of the alkyl groups attached to boron increase
40 ion of the substrate entry pore size and the bulkiness of the gating residues.
41 ntered on the isopropyl carbon in 2b and the bulkiness of the isopropyl group prevent the necessary r
42 aromaticity of the ligand and less so on the bulkiness of the ligand.
43 tivity can be achieved by varying the steric bulkiness of the ligand.
44                                          The bulkiness of the N-(1-alkyl) substituent was found to (a
45 report a series of molecules with increasing bulkiness of the peripheral side chains exhibiting incre
46 ylated clusters is observed depending on the bulkiness of the phosphine's alkyl substituents and on t
47 a high volume of disease and potentially the bulkiness of the primary tumour.
48 rbene intermediate, which is enhanced by the bulkiness of the R group.
49 steric effect is described as the sum of the bulkiness of the R1 and R2 groups (i.e., normal steric e
50              The nature of the metal and the bulkiness of the residues at the tetramic acid chelator
51 he nature of nucleophiles and (2) the steric bulkiness of the substituents at C-2 and C-4 of the cycl
52 droxide are largely influenced by the steric bulkiness of the substituents at C-2 and C-4 of the cycl
53  upon either migratory ability or the steric bulkiness of the substituents at C1 and C5.
54 or the diastereoselectivity with the greater bulkiness of the substituents giving higher diastereosel
55 lectivity of the reaction increased with the bulkiness of the substituents of the aldehyde donor in t
56 l substitutions resulting from the different bulkiness of the substituents were demonstrated by the X
57 arameters of PSII function in these mutants, bulkiness of the substituted amino acids is highly corre
58             In spite of the apparent similar bulkiness of the two substituents, most of the derivativ
59                                 However, the bulkiness of the W1 region implies that the DNA conforma
60 electivity among inorganic cations or on the bulkiness of their acidic side chains at the locus of se
61 aining patterns were created based upon the "bulkiness" of the individual amino acid side-chains in t
62                  The impact of remote steric bulkiness on the Cu-H insertion rate is analyzed, reveal
63 r reactions because the substituent's steric bulkiness raises the activation energy of the favored C-
64 tilized, they still suffer from rigidity and bulkiness to mitigate post-EVD placement trauma.
65 based ligands by fine-tuning the substituent bulkiness, which enables the quantitative formation of r
66      T(g) was greatly affected by side-chain bulkiness, with values ranging from 39 to 139 degrees C.