ライフサイエンスコーパス: ketone group

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 ving addition of a vinyl anion to a proximal ketone group.

5 These can be hydroxyl or ketone groups.

6 ly, resulting in the cell surface display of ketone groups.

7 ompounds containing at least one aldehyde or ketone groups.

8 Incorporation of the ketone group allows for subsequent modification via bio-

9 d for the synthesis of pyridazines bearing a ketone group and different methods of cyclization were c

10 mimetics possessing a heterocycle-activated ketone group and identified in particular benzothiazole

11 cy depending on both position of the central ketone groups and the number and positions of lateral me

12 e phosphate group is out of the plane of the ketone group, and the hydroxy and ketone oxygen atoms ar

13 with biotin through selective conjugation to ketone groups, and selectively killed in the presence of

14 educible functional groups such as imine and ketone groups are present in the same molecule, this cat

15 orcholanes containing a ketone or conjugated ketone group at C-20, C-22, C-23, or C-24 were prepared

16 eatures that were identified included: (1) a ketone group at position C-16, (2) an axial 4alpha-OMe g

17 Here we show that cell-surface ketone groups can be recycled back to the cell membrane

18 The recycled ketone groups could then mediate targeted conjugation of

19 thesis of organosilicon compounds, bearing a ketone group distally substituted with a silyl group wit

20 Further functionalization of the ketone group enables access to other useful fluorinated

21 o acetylenes activated by sulfone, ester, or ketone groups, followed by intramolecular arylation, aff

22 of polyketide elongation, indicating the C2' ketone group found in (R)-monocillin II is incorporated

23 r was successfully reduced by introducing an ketone group in place of the ester group.

24 For compounds bearing ketone groups in addition to carboxylic and hydroxyl gro

25 fication of analytes containing aldehyde and ketone groups in biological samples by adding chemical i

26 reactivity differences between photoreactive ketone groups in specific chemical environments.

27 Finally, after reduction of the generated ketone group into the corresponding carbinol, the effect

28 opose that the incorporation of nitroxide or ketone groups into the hydrocarbon region near the lipid

29 The introduction of ketone groups into the polymer backbone allows these mat

30 d identify molecules containing aldehyde and ketone groups is demonstrated using 61 target analytes f

31 roups, including cyano, ester, aldehyde, and ketone groups, occurs under relatively mild reaction con

32 The ketone group of the products serves as a convenient hand

33 ay be due to misalignment of the hydroxyl or ketone group of the substrate with the appropriate catal

34 that the site of reduction is the exocyclic ketone group of the tetrahydrocorphin.

35 eved by forming an oxime linkage between the ketone groups of transaminated amino donors and a probe

36 The ketone group on the cell surface can then be covalently

37 gar decorated the cell surface with a unique ketone group that served as a foundation on which we bui

38 bed method, we delivered a uniquely reactive ketone group to endogenous cell surface sialic acid resi

39 ibenzosuberenone, bearing a beta-amino-alpha-ketone group was secured by X-ray crystallography.

40 ivative of N-acetyl-mannosamine, which has a ketone group, was converted to the corresponding sialic