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1 ical olefin-addition reactions with bromine, sulfuryl chloride, m-chloroperbenzoic acid, dioxygen, an
2 nly used S(VI) electrophiles, and the parent sulfuryl chloride, O2 S(VI) Cl2 , has also been relied o
3 heteroarenes in good yield by treatment with sulfuryl diimidazole in nonpolar solvents at elevated te
5 CoA that was competitive with respect to the sulfuryl donor substrate, 3'-phosphoadenosine-5'-phospho
6 constants for hydrolysis of a wide range of sulfuryl esters, ArOSO(2)X(-), are shown to be correlate
7 od for the deoxyfluorination of phenols with sulfuryl fluoride (SO2F2) and tetramethylammonium fluori
8 etramethylammonium 2,6-dimethylphenoxide and sulfuryl fluoride (SO2F2) serves as a particularly pract
10 density of this oxygen atom on a transferred sulfuryl group accounts for a large fraction of the decr
14 gi enzymes that catalyze the transfer of the sulfuryl group from 3'-phosphoadenosine 5'-phosphosulfat
15 nsferase (EST) catalyzes the transfer of the sulfuryl group from 3'-phosphoadenosine 5'-phosphosulfat
16 roup of enzymes catalysing the transfer of a sulfuryl group from 3'-phosphoadenosine 5'-phosphosulpha
17 Sulfotransferases catalyze the transfer of a sulfuryl group from the eukaryotic sulfate donor 3'-phos
18 phoadenosine 5'-phosphosulfate (PAPS), whose sulfuryl group is reduced or transferred to other metabo
19 ansferase (EST) catalyzes transfer of the 5'-sulfuryl group of adenosine 3'-phosphate 5'-phosphosulfa
22 isotope effects support the notion that the sulfuryl group resembles SO(3) in the transition state.
23 s of enzymes that catalyze the transfer of a sulfuryl group to a hydroxyl or amine moiety on various
24 -3), a key sulfotransferase that transfers a sulfuryl group to a specific glucosamine in HS generatin
25 directions indicates that the transfer of a sulfuryl group to an aryl hydroxyl group catalyzed by be
27 ohydrate sulfotransferase Stf0 catalyzes the sulfuryl group transfer from 3'-phosphoadenosine-5'-phos
28 measured, and the catalytic mechanism of the sulfuryl group transfer reaction was investigated in ini
31 catalytic histidine residue, (2) an in-line sulfuryl-group transfer mechanism, and (3) constraints i
32 rases in liver and catalyzes transfer of the sulfuryl moiety (-SO(3)) from activated sulfate (PAPS, 3
33 solic sulfotransferases (SULTs) transfer the sulfuryl moiety (-SO(3)) from activated sulfate [3'-phos
34 ysiological relevance by the transfer of the sulfuryl moiety (-SO(3)) from PAPS (3'-phosphoadenosine
35 ignaling small molecules via transfer of the sulfuryl moiety (-SO3) from 3'-phosphoadenosine 5'-phosp
36 of signaling metabolites via transfer of the sulfuryl moiety (-SO3) from activated sulfate (3'-phosph
37 s and other xenobiotics--by transferring the sulfuryl moiety (SO3) from 3'-phosphoadenosine 5'-phosph
38 ults show that while the interactions of the sulfuryl moiety and the phenyl ring with the YopH active
39 network with the hydroxyl group ortho to the sulfuryl moiety, which may be exploited to design more p
40 switched "on" and "off" via transfer of the sulfuryl-moiety (-SO3) from PAPS (3'-phosphoadenosine 5'
41 ll kinetic isotope effect in the nonbridging sulfuryl oxygen atoms suggests no significant change in
42 for the estrogen sulfotransferase-catalyzed sulfuryl (SO3) transfer from p-nitrophenyl sulfate to th
43 faster than the aqueous reaction, while the sulfuryl transfer from the pNPS anion is some 40-fold sl
48 on of the data for enzymatic and uncatalyzed sulfuryl transfer reactions suggests that both proceed t
50 ups are aryl groups the hydrolysis reaction (sulfuryl transfer to water) occurs by way of attack at s
53 echanistic similarities, the phosphoryl- and sulfuryl-transfer reactions differ markedly in their res
54 ts and medium effects have been measured for sulfuryl-transfer reactions of the sulfate ester p-nitro
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