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1 ism of para-disubstituted benzenes such as p-methylstyrene.
2 -dimethylstyrene, 4-tert-butylstyrene, and 3-methylstyrene.
3 III) salen-catalyzed epoxidation of cis-beta-methylstyrene.
4 ne monomers: styrene, 2,5-dimethylstyrene, 4-methylstyrene, 2,4-dimethylstyrene, 4-tert-butylstyrene,
5 mihydrogenate 1-phenyl-1-propyne to cis-beta-methylstyrene (20 bar H2, 40 degrees C) with turnover nu
7 e compromised by polymerization of the alpha-methylstyrene, a process favored by tetrahydrofuran (THF
8 ino)naphthalenide (LDMAN), is added to alpha-methylstyrene, a tandem addition/cyclization to a phenyl
9 y incorporating a minimal amount of an alpha-methylstyrene (AMS) analogue into the polymer structure.
11 and without allylic C-H groups, namely beta-methylstyrene and styrene, respectively, was investigate
12 -mediated sulfonylation of substituted alpha-methylstyrenes and sodium sulfinates (RSO2Na) in MeCN wi
13 ly grafted copolymers, polyethylene-g-poly(4-methylstyrene) and polyethylene-g-poly(methyl methacryla
14 arable conditions alpha-methylstyrene, trans-methylstyrene, and allylbenzene behave very differently
15 )-dependent epoxidation of styrene, cis-beta-methylstyrene, and cis-stilbene with retention of stereo
17 rom the reaction of 1 with styrene and alpha-methylstyrene are formulated as [(PhNO)3Cu(eta(2)-alkene
18 tion, we applied a commodity chemical, alpha-methylstyrene, as a methylation reagent to prepare methy
19 s of Rh-(S,S)-YanPhos-catalyzed AHF of alpha-methylstyrene, as obtained through a comprehensive DFT (
20 end consisting of polystyrene and poly(alpha-methylstyrene), both polymers having similar molecular w
21 ms in THF due to polymerization of the alpha-methylstyrene, but moderate yields are attained in a sol
22 nchains 15.4% more styrene (B), 28.9% more 4-methylstyrene (C), 45.4% more 4-fluorostyrene (D), 41.2%
24 mulations of an explicitly solvated cis-beta-methylstyrene/chloroperoxidase-Compound I complex are pe
25 d by hypercrosslinking from a generic poly(4-methylstyrene-co-vinylbenzyl chloride-co-divinylbenzene)
26 h three aromatic VOCs - styrene, o-xylene, a-methylstyrene - highlighted for the two a-HBCDD doses.
27 ree aromatic VOCs - styrene, o-xylene, alpha-methylstyrene - highlighted for the two alpha-HBCDD dose
29 on of the dimethyl ether in vacuo, the alpha-methylstyrene is added and the solution is warmed to -30
31 3), CPO's enantiospecificity toward cis-beta-methylstyrene is likely to be caused by a specific group
32 olefins with allylic C-H groups (e.g., beta-methylstyrene) is independent of the surface OH density
34 secutive chain transfer reaction, first to p-methylstyrene (or styrene) and then to hydrogen, during
36 ular mechanics calculations of 1S,2S-trans-2-methylstyrene oxide in the active site of murine epoxide
37 S(N)2 reaction of acetate with 1S,2S-trans-2-methylstyrene oxide to provide the corresponding diol ac
39 ersely proportional to the molar ratio of [p-methylstyrene]/[propylene] and [styrene]/[propylene] wit
40 i NCIs between the chiral catalyst and alpha-methylstyrene render the si-face binding to the Rh-cente
41 ns from the reactions of trans- and cis-beta-methylstyrene reveal that the reaction proceeds, at leas
42 lorination of simple, unfunctionalized alpha-methylstyrene, the same pattern of cage reactivity is ob
43 ve rates of oxidation of cis- and trans-beta-methylstyrenes together with the rho value of a series o
44 found that under comparable conditions alpha-methylstyrene, trans-methylstyrene, and allylbenzene beh
45 quential reaction was also completed where p-methylstyrene was oxidized to 4'-methyl-acetophenone by
46 anthracenes and beta-sulfonylation of alpha-methylstyrene were successfully carried out in aqueous m
48 tic activity for the hydroarylation of alpha-methylstyrene with N,N-dimethylaniline, and the copper(I