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1 be exploited for the isotope labeling of the aldehyde group.
2 ine of a polypeptide chain to a ketone or an aldehyde group.
3 ns by FGE produced products bearing a unique aldehyde group.
4 ed carbon-palladium bond to a tethered cyano/aldehyde group.
5 with glutaraldehyde to introduce a layer of aldehyde groups.
6 rried out regioselectively at one of the two aldehyde groups.
7 mines to polyacrylamide gel derivatized with aldehyde groups.
9 the adduct ion formed from a reagent with an aldehyde group and a peptide ion with a primary amine gi
10 ehyde phosphate, followed by rotation of the aldehyde group and condensation to the epimer at C-4.
11 l is highly toxic due to its highly reactive aldehyde group and has to be detoxified by either reduct
12 etylene-based framework carries two terminal aldehyde groups and provides a strong chiroptical respon
13 ide chain carboxyl group and formation of an aldehyde group at the carbon next to the original carbox
14 containing acid, ester, amide, carbinol, and aldehyde groups at the 3-position of the quinoline ring
15 (iii) Indirect product labeling of released aldehyde groups by hydrazone formation with an acridone-
17 e 1, in which tightly held acylguanidine and aldehyde groups engage in multiple intramolecular hydrog
18 ionalizations of a methyl, hydroxymethyl, or aldehyde group has been developed providing a general ac
24 proach, a cemadotin derivative containing an aldehyde group is joined via a thiazolidine linkage.
27 e other hand, substituents such as vinyl and aldehyde groups lead to essentially no difference in the
28 and Arg side chains of proteins/peptides and aldehyde groups linked to 7-deazaguanine residues in DNA
33 lowing formation of a Schiff base between an aldehyde group of the AP site and an amino group of the
34 alent imine/enamine adduct (E.I) between the aldehyde group of the inhibitor and the guanidine group
35 with the formation of an enamine between the aldehyde group of the inhibitor and the guanidine group
36 Tyr212 is positioned to interact with the aldehyde group of the substrate and polarize it for reac
37 used by a Schiff's base reaction between the aldehyde groups of reducing sugars and the primary amine
38 be used to postsynthetically cross-link the aldehyde groups of ZIF-90 using a diamine molecule with
39 suggest that interactions with a sialic acid aldehyde group on mildly oxidized ligands that include i
40 on the formation of hydrazone bonds between aldehyde groups on the Fc moieties of periodate-oxidized
41 mically functionalized with methacrylate and aldehyde groups on the polysaccharide backbone to chemic
42 been used to probe the presence of amine and aldehyde groups on the surface after CVD polymerization
43 this chemistry (2a,b and 18a,b) contain two aldehyde groups, one of which exists as a hemiacetal.
44 where control over the fraction of azide and aldehyde groups per nanocrystal can be easily achieved:
45 containing a conjugated carboxylic ester or aldehyde group proceed to provide the desired 1,4-diene
50 evelopment of substituents near the reactive aldehyde group that either transfer protons at the trans
51 patterned PCysMA brushes functionalized with aldehyde groups that enable conjugation to green fluores
52 njugated backbone was functionalized with an aldehyde group to render the molecule nonfluorescent.
53 talyzes the oxidation of the C8 methyl to an aldehyde group via two discrete monooxygenase reactions.
54 ides were immobilized on glass slides having aldehyde groups via transient Schiff base formation foll
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