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1  a new AdoMet analogue functionalized with a ketone group.
2 of GlcNAc, is a novel GlcNAc analogue with a ketone group.
3 ond ester group must arise from the original ketone group.
4                     These can be hydroxyl or ketone groups.
5 ly, resulting in the cell surface display of ketone groups.
6 ompounds containing at least one aldehyde or ketone groups.
7                         Incorporation of the ketone group allows for subsequent modification via bio-
8 d for the synthesis of pyridazines bearing a ketone group and different methods of cyclization were c
9  mimetics possessing a heterocycle-activated ketone group and identified in particular benzothiazole
10 cy depending on both position of the central ketone groups and the number and positions of lateral me
11 e phosphate group is out of the plane of the ketone group, and the hydroxy and ketone oxygen atoms ar
12 with biotin through selective conjugation to ketone groups, and selectively killed in the presence of
13 educible functional groups such as imine and ketone groups are present in the same molecule, this cat
14 orcholanes containing a ketone or conjugated ketone group at C-20, C-22, C-23, or C-24 were prepared
15 eatures that were identified included: (1) a ketone group at position C-16, (2) an axial 4alpha-OMe g
16 o acetylenes activated by sulfone, ester, or ketone groups, followed by intramolecular arylation, aff
17 of polyketide elongation, indicating the C2' ketone group found in (R)-monocillin II is incorporated
18 r was successfully reduced by introducing an ketone group in place of the ester group.
19                        For compounds bearing ketone groups in addition to carboxylic and hydroxyl gro
20 fication of analytes containing aldehyde and ketone groups in biological samples by adding chemical i
21    Finally, after reduction of the generated ketone group into the corresponding carbinol, the effect
22 opose that the incorporation of nitroxide or ketone groups into the hydrocarbon region near the lipid
23 d identify molecules containing aldehyde and ketone groups is demonstrated using 61 target analytes f
24 roups, including cyano, ester, aldehyde, and ketone groups, occurs under relatively mild reaction con
25                                          The ketone group of the products serves as a convenient hand
26 ay be due to misalignment of the hydroxyl or ketone group of the substrate with the appropriate catal
27  that the site of reduction is the exocyclic ketone group of the tetrahydrocorphin.
28                                          The ketone group on the cell surface can then be covalently
29 gar decorated the cell surface with a unique ketone group that served as a foundation on which we bui
30 bed method, we delivered a uniquely reactive ketone group to endogenous cell surface sialic acid resi
31 ivative of N-acetyl-mannosamine, which has a ketone group, was converted to the corresponding sialic

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