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1 through the fine-tuning of the reactivity of sulfuryl chloride (SO(2)Cl(2)) by organocatalysts.
2 glycosyl chlorides from thioglycosides using sulfuryl chloride at rt.
3 ical olefin-addition reactions with bromine, sulfuryl chloride, m-chloroperbenzoic acid, dioxygen, an
4 nly used S(VI) electrophiles, and the parent sulfuryl chloride, O2 S(VI) Cl2 , has also been relied o
5  hair exposed to chlorine, hypochlorite, and sulfuryl chloride.
6 lpha-haloketones, a silyl chloride, acyl and sulfuryl chlorides, and a nitroarene.
7 heteroarenes in good yield by treatment with sulfuryl diimidazole in nonpolar solvents at elevated te
8                           PAPS serves as the sulfuryl donor for the biosynthesis of all sulfate ester
9 CoA that was competitive with respect to the sulfuryl donor substrate, 3'-phosphoadenosine-5'-phospho
10  constants for hydrolysis of a wide range of sulfuryl esters, ArOSO(2)X(-), are shown to be correlate
11 aration of this reagent relies on the use of sulfuryl fluoride (SO(2)F(2)), which is difficult to obt
12                                              Sulfuryl fluoride (SO(2)F(2), SF) is an effective and in
13 od for the deoxyfluorination of phenols with sulfuryl fluoride (SO2F2) and tetramethylammonium fluori
14 etramethylammonium 2,6-dimethylphenoxide and sulfuryl fluoride (SO2F2) serves as a particularly pract
15 imple to perform, as recently exemplified by sulfuryl fluoride exchange chemistry.
16                                              Sulfuryl fluoride is a valuable reagent for the one-pot
17                    This enzyme transfers the sulfuryl group (SO(3)) from 3'-phosphoadenosine 5'-phosp
18 density of this oxygen atom on a transferred sulfuryl group accounts for a large fraction of the decr
19                                The universal sulfuryl group donor for SULT-catalyzed sulfation is ade
20                                The universal sulfuryl group donor for SULTcatalyzed sulfation is aden
21                    In mammals, the universal sulfuryl group donor molecule 3'-phosphoadenosine 5'-pho
22 gi enzymes that catalyze the transfer of the sulfuryl group from 3'-phosphoadenosine 5'-phosphosulfat
23 nsferase (EST) catalyzes the transfer of the sulfuryl group from 3'-phosphoadenosine 5'-phosphosulfat
24 roup of enzymes catalysing the transfer of a sulfuryl group from 3'-phosphoadenosine 5'-phosphosulpha
25 Sulfotransferases catalyze the transfer of a sulfuryl group from the eukaryotic sulfate donor 3'-phos
26 phoadenosine 5'-phosphosulfate (PAPS), whose sulfuryl group is reduced or transferred to other metabo
27 ansferase (EST) catalyzes transfer of the 5'-sulfuryl group of adenosine 3'-phosphate 5'-phosphosulfa
28 S/MS) analysis under conditions in which the sulfuryl group of sulfotyrosine is labile.
29                               Receipt of the sulfuryl group often radically alters acceptor-target in
30  isotope effects support the notion that the sulfuryl group resembles SO(3) in the transition state.
31 s of enzymes that catalyze the transfer of a sulfuryl group to a hydroxyl or amine moiety on various
32 -3), a key sulfotransferase that transfers a sulfuryl group to a specific glucosamine in HS generatin
33  directions indicates that the transfer of a sulfuryl group to an aryl hydroxyl group catalyzed by be
34                          NodST catalyzes the sulfuryl group transfer from 3'-phosphoadenosine 5'-phos
35 ohydrate sulfotransferase Stf0 catalyzes the sulfuryl group transfer from 3'-phosphoadenosine-5'-phos
36 measured, and the catalytic mechanism of the sulfuryl group transfer reaction was investigated in ini
37   Arg78 is in close proximity to the site of sulfuryl group transfer.
38 tem since no shift in absorption accompanies sulfuryl group transfer.
39  catalytic histidine residue, (2) an in-line sulfuryl-group transfer mechanism, and (3) constraints i
40 rases in liver and catalyzes transfer of the sulfuryl moiety (-SO(3)) from activated sulfate (PAPS, 3
41 solic sulfotransferases (SULTs) transfer the sulfuryl moiety (-SO(3)) from activated sulfate [3'-phos
42 ysiological relevance by the transfer of the sulfuryl moiety (-SO(3)) from PAPS (3'-phosphoadenosine
43 ignaling small molecules via transfer of the sulfuryl moiety (-SO3) from 3'-phosphoadenosine 5'-phosp
44 of signaling metabolites via transfer of the sulfuryl moiety (-SO3) from activated sulfate (3'-phosph
45 s and other xenobiotics--by transferring the sulfuryl moiety (SO3) from 3'-phosphoadenosine 5'-phosph
46 ults show that while the interactions of the sulfuryl moiety and the phenyl ring with the YopH active
47 network with the hydroxyl group ortho to the sulfuryl moiety, which may be exploited to design more p
48  switched "on" and "off" via transfer of the sulfuryl-moiety (-SO3) from PAPS (3'-phosphoadenosine 5'
49 ll kinetic isotope effect in the nonbridging sulfuryl oxygen atoms suggests no significant change in
50  for the estrogen sulfotransferase-catalyzed sulfuryl (SO3) transfer from p-nitrophenyl sulfate to th
51  faster than the aqueous reaction, while the sulfuryl transfer from the pNPS anion is some 40-fold sl
52                 Understanding phosphoryl and sulfuryl transfer is central to many biochemical process
53 istic of the transition state for an in-line sulfuryl transfer reaction from PAPS to E2.
54  in position to play a catalytic role in the sulfuryl transfer reaction of EST.
55                                              Sulfuryl transfer reactions of sulfate diesters (RO-SO(2
56 on of the data for enzymatic and uncatalyzed sulfuryl transfer reactions suggests that both proceed t
57 del systems for understanding phosphoryl and sulfuryl transfer reactions, respectively.
58 ups are aryl groups the hydrolysis reaction (sulfuryl transfer to water) occurs by way of attack at s
59 PAPS and K(I) values for PAP, the product of sulfuryl transfer.
60 at can be used to regulate specific areas of sulfuryl-transfer metabolism.
61 echanistic similarities, the phosphoryl- and sulfuryl-transfer reactions differ markedly in their res
62 ts and medium effects have been measured for sulfuryl-transfer reactions of the sulfate ester p-nitro