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1 ng or an open-ring sugar with a reactive C1' aldehyde group.
2 ed carbon-palladium bond to a tethered cyano/aldehyde group.
3 be exploited for the isotope labeling of the aldehyde group.
4 ine of a polypeptide chain to a ketone or an aldehyde group.
5 ns by FGE produced products bearing a unique aldehyde group.
6 om large Criegee intermediates containing an aldehyde group.
7 with glutaraldehyde to introduce a layer of aldehyde groups.
8 rried out regioselectively at one of the two aldehyde groups.
9 mines to polyacrylamide gel derivatized with aldehyde groups.
10 ions) liberates the SBUs functionalized with aldehyde groups.
11 nearly hydrophobic dioxane side has terminal aldehyde groups.
12 copolymer with a tunable fraction of pendant aldehyde groups (12-64%) using controlled radical polyme
14 Fs through imine condensation reactions with aldehyde groups anchored in the COF pores, followed by i
15 the adduct ion formed from a reagent with an aldehyde group and a peptide ion with a primary amine gi
16 ehyde phosphate, followed by rotation of the aldehyde group and condensation to the epimer at C-4.
17 l is highly toxic due to its highly reactive aldehyde group and has to be detoxified by either reduct
18 etylene-based framework carries two terminal aldehyde groups and provides a strong chiroptical respon
19 However, most reported polymers comprising aldehyde groups are based on either end-group-modified s
21 ich chiral-at-ruthenium complex featuring an aldehyde group as a versatile asymmetric catalyst with r
22 ide chain carboxyl group and formation of an aldehyde group at the carbon next to the original carbox
23 containing acid, ester, amide, carbinol, and aldehyde groups at the 3-position of the quinoline ring
24 (iii) Indirect product labeling of released aldehyde groups by hydrazone formation with an acridone-
27 e 1, in which tightly held acylguanidine and aldehyde groups engage in multiple intramolecular hydrog
28 es and direct N-terminal incorporation of an aldehyde group for orthogonal bioconjugation reactions.
30 c polyaza cage is decorated with exoextended aldehyde groups for membrane fabrication and multiple am
31 with a blank copy strand equipped with three aldehyde groups for the reversible attachment of amine r
32 ionalizations of a methyl, hydroxymethyl, or aldehyde group has been developed providing a general ac
33 region of the antibody to produce functional aldehyde groups; (ii) attachment of a heterobifunctional
38 ker, aminooxy-PEG-dibenzocyclooctyne, to the aldehyde groups in the Fc moiety; and (iii) click conjug
40 the intrinsic, high electrophilicity of the aldehyde group is associated with safety concerns and me
43 proach, a cemadotin derivative containing an aldehyde group is joined via a thiazolidine linkage.
47 e other hand, substituents such as vinyl and aldehyde groups lead to essentially no difference in the
48 and Arg side chains of proteins/peptides and aldehyde groups linked to 7-deazaguanine residues in DNA
52 ve nucleophilic additions of indoles with an aldehyde group of ortho-formylarylketones, and the keton
54 lowing formation of a Schiff base between an aldehyde group of the AP site and an amino group of the
55 epsilon-nitrogen of active site K127 and the aldehyde group of the enal dienophile was revealed by st
56 alent imine/enamine adduct (E.I) between the aldehyde group of the inhibitor and the guanidine group
57 with the formation of an enamine between the aldehyde group of the inhibitor and the guanidine group
58 Tyr212 is positioned to interact with the aldehyde group of the substrate and polarize it for reac
59 platform and anti-CDH22 antibodies bound to aldehyde groups of benzaldehyde substituted poly(phospha
60 molecules slowly diffuse away, exposing the aldehyde groups of BNPs, which can bind to amine groups
61 used by a Schiff's base reaction between the aldehyde groups of reducing sugars and the primary amine
62 be used to postsynthetically cross-link the aldehyde groups of ZIF-90 using a diamine molecule with
63 suggest that interactions with a sialic acid aldehyde group on mildly oxidized ligands that include i
65 on the formation of hydrazone bonds between aldehyde groups on the Fc moieties of periodate-oxidized
66 mically functionalized with methacrylate and aldehyde groups on the polysaccharide backbone to chemic
67 been used to probe the presence of amine and aldehyde groups on the surface after CVD polymerization
68 this chemistry (2a,b and 18a,b) contain two aldehyde groups, one of which exists as a hemiacetal.
69 where control over the fraction of azide and aldehyde groups per nanocrystal can be easily achieved:
70 containing a conjugated carboxylic ester or aldehyde group proceed to provide the desired 1,4-diene
71 g a phenyl group at the alpha-position of an aldehyde group reacts more readily with indoles to form
76 evelopment of substituents near the reactive aldehyde group that either transfer protons at the trans
78 ere kinetic products with multiple unreacted aldehyde groups that acted as hydrogen bond donors and a
79 patterned PCysMA brushes functionalized with aldehyde groups that enable conjugation to green fluores
80 njugated backbone was functionalized with an aldehyde group to render the molecule nonfluorescent.
81 talyzes the oxidation of the C8 methyl to an aldehyde group via two discrete monooxygenase reactions.
82 ides were immobilized on glass slides having aldehyde groups via transient Schiff base formation foll
85 rivative containing two electron-withdrawing aldehyde groups was found to exhibit versatile solid-sta
86 statistical copolymers bearing cis-diol and aldehyde groups was prepared using sub-stoichiometric pe
87 ary amine-based reagents that react with the aldehyde group, we uncovered evidence for abasic sites i
89 he flax mucilage undergoes oxidation to form aldehyde groups, which then react with zein's amino grou