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2- naphthyl phenyl

Figure 6.10. Rate constants for quenching of sensitizers by cis- and trans-stilbenes (open and filled circles, respectively). Sensitizers are as follows (1) tri-phenylene, (2) thioxanthone, (3) phenanthrene, (4) 2-acetonaphthone, (3) 1-naphthyl phenyl ketone, (6) crysene, (7) fluorenone, (8) 1,2,5,6-dibenzanthracene, (9) benzil, (10) 1,2,3,4-dibenzanthracene, (11) pyrene, (12) 1,2-benzanthracene, (13) benzanthrone, (14) 3-acetyl pyrene, (15) acridine, (16) 9,10-dimethyl-l,2-benzanthracene, (17) anthracene, (18) 3,4-benzpyrene.<57> Reprinted by permission of the American Chemical Society. Figure 6.10. Rate constants for quenching of sensitizers by cis- and trans-stilbenes (open and filled circles, respectively). Sensitizers are as follows (1) tri-phenylene, (2) thioxanthone, (3) phenanthrene, (4) 2-acetonaphthone, (3) 1-naphthyl phenyl ketone, (6) crysene, (7) fluorenone, (8) 1,2,5,6-dibenzanthracene, (9) benzil, (10) 1,2,3,4-dibenzanthracene, (11) pyrene, (12) 1,2-benzanthracene, (13) benzanthrone, (14) 3-acetyl pyrene, (15) acridine, (16) 9,10-dimethyl-l,2-benzanthracene, (17) anthracene, (18) 3,4-benzpyrene.<57> Reprinted by permission of the American Chemical Society.
NiBr, 160 1 -Naphthyl-phenyl-phosphin-sdure-ethylester 94 (Schmp. 180-183°) 51 ... [Pg.201]

Naphthyl-phenyl- XII/1, 238 1-Naphthyl-phenyl- -ethylester E2, 201 1-Naphthyl-trichlormethyl- -butylester E2, 203 [ -(4-Nitro-anilino)-benzyl]-phenyl- E2, 129 (2-Nitro-l-phenyl-ethyl)-phenyl- -ethylester E2,... [Pg.1025]

Naphthyl phenyl sulfide is desulfurized to naphthalene on refluxing with lithium aluminum hydride and titanium tetrachloride, and 1-naphthyl ethyl sulfide and 1-naphthyl isopropyl sulfide are converted to naphthalene on treatment with ethanethiol and anhydrous aluminum chloride (equation 83). ... [Pg.914]

Benz[de]anthrone 272 A finely divided mixture of 1-naphthyl phenyl ketone (1 part) and anhydrous aluminum chloride (5 parts) is heated, with protection by a calcium chloride tube, during 0.5 h from 60° to 115°, during a further 1 h from 115° to 130°, and during a final 1 h from 130° to 150°. The cake is decomposed by dilute hydrochloric acid, and the resulting solid is filtered off and washed with alcohol and ether it then consists of moderately pure benzanthrone (yield 76%). Recrystallization from glacial acetic acid, with charcoal, affords the pure compound as pale brown needles, m.p. 167-168° (uncorr.). [Pg.897]

Scholl reactions generally lead to six-membered rings but a few cases have been reported where five-membered rings were formed, particularly from ketones that carried a hydroxyl or an alkoxyl group para to the carbonyl group, such a case was reported by Fierz-David and Jaccard275 who found that 4-hydroxy-1-naphthyl phenyl ketone (and its methyl ether) gave 5-hydroxy-benzo[a]fluoren-l 1-one and not 4-hydroxybenz[de]anthrone ... [Pg.898]

Figure 4. Diasteieomeric Splitting of Methyl Groups in Isopropyl of Methyl( 1 -naphthyl)phenyl-(-)-menthyloxysilane. Figure 4. Diasteieomeric Splitting of Methyl Groups in Isopropyl of Methyl( 1 -naphthyl)phenyl-(-)-menthyloxysilane.
Synthesis of heptaisobutyl[2- 4-( 1-naphthyl)phenyl ethenyl] octasilsesquioxane via silylaiJve coupling of monovinylheptaisobutylsilsesquioxane with 1-(4-vinylphenyl) naphthalene Reaction Scheme 2 ... [Pg.149]


See other pages where 2- naphthyl phenyl is mentioned: [Pg.241]    [Pg.422]    [Pg.700]    [Pg.710]    [Pg.1634]    [Pg.551]    [Pg.559]    [Pg.410]    [Pg.551]    [Pg.559]    [Pg.1088]    [Pg.650]    [Pg.123]    [Pg.175]    [Pg.305]    [Pg.65]    [Pg.122]    [Pg.175]    [Pg.305]    [Pg.425]    [Pg.170]    [Pg.629]    [Pg.216]    [Pg.1634]    [Pg.445]    [Pg.242]   
See also in sourсe #XX -- [ Pg.334 , Pg.410 , Pg.551 , Pg.559 ]

See also in sourсe #XX -- [ Pg.334 , Pg.410 , Pg.551 , Pg.559 ]




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1- Naphthyl phenyl amine

2-Naphthyl

5-naphthyl-3-phenyl- -chloride

Naphthyl-phenyl-ketone

Phenyl- and 2,7-Naphthyl-Linked Dimeric Cinchona-PTCs

Sulfide, 1-naphthyl phenyl

Sulfide, 1-naphthyl phenyl desulfurization

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