1                          The cysteine thiols were alkylated with 3-bromo-1,1,1-trifluoroacetone to at

2 pproach the nitrogen of the starting pyrrole was alkylated with a special Michael acceptor having an

3  the thiocarbonyl group of the modified base was alkylated with a variety of alpha-bromoacetyl-deriva

4 sible cysteine residues in alphabeta tubulin were alkylated with an excess of iodoacetamide to preven

5                        Diverse ketones could be alkylated with diarylmethanols, cinnamyl alcohols, an

6             A series of substituted quinones was alkylated with diethylcadmium.

7                                Intermediates were alkylated with either N-phenylmaleimide or 4-vinylp

8 lated with BBr(3), and the resulting phenols were alkylated with ethyl bromoacetate.

9 vage (LDC), is presented in which DNA or RNA is alkylated with fluorescent tags and fragmented in the

10 trate in which the free thiol molecules have been alkylated with iodoacetamide.

11 ion mediated by OONO(-), nitrated complex II was alkylated with iodoacetamide.

12                                       When 1 is alkylated with LiCH2SiMe3 and KCH2Ph, the complexes (

13 the cysteines of the active-site dithiol has been alkylated with N-ethylmaleimide (NEM).

14 f the cysteines of the active-site disulfide is alkylated with N-ethylmaleimide (NEM-FTR).

15                 Specifically, N-arylpyrroles were alkylated with N-acryloyl-1H-pyrazole electrophiles

16              Reduced Cys in the D'D3 monomer were alkylated with N-ethylmaleimide and analyzed by mas

17 nalogue was observed when the catalytic site was alkylated with p-bromophenacyl bromide.

18                                 This in turn was alkylated with the appropriate benzyl halide to affo

19 condary role: Indole and pyrrole derivatives are alkylated with unactivated secondary aliphatic alcoh