4.5- diphenyl-1-propyl

Carbocyclische Kationen lassen sich ebenfalls reduktiv dimerisieren z. B. Triphenyl-cyclopropenium-, Diphenyl-propyl-cyclopropenium- und Phenyl-dipropyl-cycloprope-nium-Kationen (Tripropyl-cyclopropenium-Kationen reagieren dagegen nicht)6. 

N-Diphenylmethylen- 374 N-Diphenylmethylen-O-aminocarbonyl- 612 N-[l,3-Diphenyl-propyl-(2) - 374 N-[l,3-Diphenyl-propyliden-(2)]- 374, 377, 380 N-(4-Halogen-phenyI)- 683 N-Heptyl- 375 N-Heptyl-N-acetyl- 376 N-Heptyliden- 375 N-Hcptyliden-O-acetyl- 376 0-(2-Hydroxy-athyl)-N-athoxycarbonyl- 133 N-(4-Hydroxy-phenyl)- 683 0-(2-Hydroxy-l-phenyl-athyI)-N-athoxycarbonyI-aus 0-(ci-AthoxycarbonyI-benzyl)-N-athoxycar-bonyl-hydroxylamin und Lithiumalanat 133 N-Isopropyl- 682 N-Isopropylidcn- 613 N-Methyl- 133, 682 O-Methyl-N-bcnzyliden- 377 O-Methyl-N-benzyliden- 375 0-Methyl-N-(4-chlor-benzyl)- 375 0-Methyl-N-(4-chlor-benzyliden)- 375 N-Methy -N,0-diacetyI- 682 N-(4-Methyl-phenyl)- 683 0-McthyI-N-( 1 -phenyl-athyliden)- 375 N-(4-Methylthio-phenyl)- 684 N-(4-Nitro-benzyl)- 374 N-[4-Nitro-benzyliden - 374, 377 N-(2-Nitro-phenyl)- 562 N-(4-Nitro-phenyl)- 682 N-Nitroso-N-cyclohexyl- 697 N-Octyl- 374 N-Octyl-(2)-N-acetyl- 376 N-Octyliden- 374 N-0ctyliden-(2)-0-acctyl- 376 N-(Pentafluor-phenyl)-0,N-diacetyl- 697 N-Phenyl- 474, 481, 682, 783 N-Phenylacetyl-O-benzoyl- 265 N-(l-Phenyl-athyl)- 374 N-(l-Phenyl-athyl)-N-acetyl- 376 N-(l-Phenyl-athyliden)-374, 613 N-( l-Phenyl-athyliden)-0-acetyl- 376 N-[ 1 -Phenyl-buten-( 1 )-yl-(3)-iden]- 582 N-f4-Phenyl-butyl-(2)-iden]- 581 N-Phcnyl-N,0-diacetyl- 682 N-(4-Phenylthio-phenyl)- 684 N-Propyl-N-cyclohexyl- 376 N-Propyl-N-isopropyl- 376 O-Sulfonyl- 481 N-(4-Sulfonyl-phenyI)- 683 N-(2-Vinyl-phenyl)- 698... 

Diphenyl-propyl- 518 Diphenyl- -tetrafluoroborat 85 Dipropyl- -perchlorat 85 Dipropyl-phenyl- 518 Triphcnyl-518f, 588, 649 Triphenyl- -bromid 85 Tri propyl - 518 Tris-[ferrocenyll- 649... 

Amino-5-[l-(2-furyl)-2-(5-nitro-2-furyl)-ethenyl]-1,3,4-o.xadiazols0 (Furamizol ) wirktbak-terizid, 2-[3-(5-Methyl-1,3,4-oxadiazol-2-yl)-3,3-diphenyl-propyl]-2-aza-bicyclo[2.2.2]octan (SC-27166 )81 ist ein Antidiarrhoicum. 

Die in Tab. 106 (S. 981) aufgefuhrten Beispiele der reduktiven Spaltung von l-Alkyl-2-(2,2-dimethyl-l,l-diphenyl-propyl)-diazenen zu primaren Aminen stellen die letzte Stufe einer Synthese von sek. oder tert.-Alkyl-aminen aus Aldehyden bzw. Ketonen dar, die nach dem folgenden, allgemeinen Schema verlauft5 das zur intermediaren Hydrazon-Bildung... 

Cyano-3,3-diphenyl-propyl) 4-phenyl-piperidine-4-carboxylic acid ethyl ester, C30H32N2O2, Mr 452.59 hydrochloride [3810-80-8], C30H32N2O2 HCI, Mr 489.06, mp 220.5-222.0 °C... 

Cyano-3,3-diphenyl-propyl)-[1,4 ]bipiperidinyl-4 -carboxylic acid amide, C27H34N4O, Mr 430.59, 149-ISO °C... 

Two Russian papers359,360 have described the synthesis and addition of acetylenic esters to dihydro-s-triazines. The triphenyl derivative 281 on heating with DEAD in ether for 3 hours gave 80% of286, presumably via 285. The diphenyl propyl derivative (282) added Michael fashion to... 

The product is dissolved in 134 ml of 96% ethanol whereupon 26.8 ml of concentrated hydrochloric acid and 201 ml of water are added while cooling with ice-water. The precipitate is filtered off and dried in vacuo at 100°C. 22.98 grams of N-[l -phenylethyl)-(l )]-l,l-diphenyl-propyl-(3)-amine hydrochloride are obtained. MP 200° to 201°C. On recrystallization from 285 ml of a 2 1 mixture of water and 96% ethanol the melting point remains unchanged. 

P-Diethyl amino ethyl diphenyl propyl acetate hydrogen chloride (SKF-525A) and toluene have inhibited benzene metabolism in rats (Gill et al. 1979 Ikeda et al. 1972). Carbon monoxide, aniline, aminopyrine, cytochrome C, and metapyrene inhibit benzene metabolism in mouse liver microsomes (Gonasun et al. 1973). Ethanol ingestion as well as dietary factors such as food deprivation and carbohydrate restriction, enhance the in vitro metabolism of benzene in rat liver microsomes (Nakajima et al. 1987). 

CnHuNO, [a.y-Diphenyl.propyl]- [4-nitro-benzoat] 9 II263. 

Triparanol l-[p-(2-diethylaniinoethoxy)plienyl]-l-(p-t[Pg.565]

The following liquids may be used (boiling points are given in parentheses) — chlorobenzene (132-3°) bromobenzene (155°) p cymene (176°) o-dichloro-benzene (180°) aniline (184°) methyl benzoate (200°) teti-alin (207°) ethyl benzoate (212°) 1 2 4-trichlorobenzene (213°) iaopropyl benzoate (218°) methyl salicylate (223°) n-propyl benzoate (231°) diethyleneglycol (244°) n-butyl benzoate (250°) diphenyl (255°) diphenyl ether (259°) dimethyl phth ate (282°) diethyl phthalate (296°) diphenylamine (302°) benzophenone (305)° benzyl benzoate (316°). 

Acrylic acid A 34 Diphenyl A 63 Methyl propyl ketone B... 

C ( propyl) N phenylmtrone to N phenylmaleimide, 46, 96 semicarbazide hydrochloride to ami noacetone hydiochlonde, 46,1 tetraphenylcyclopentadienone to diphenyl acetylene, 46, 44 Alcohols, synthesis of equatorial, 47, 19 Aldehydes, aromatic, synthesis of, 47, 1 /3-chloro a,0 unsaturated, from ke tones and dimethylformamide-phosphorus oxy chloride, 46, 20 from alky 1 halides, 47, 97 from oxidation of alcohols with dimethyl sulfoxide, dicyclohexyl carbodumide, and pyndimum tnfluoroacetate, 47, 27 Alkylation, of 2 carbomethoxycyclo pentanone with benzyl chloride 45,7... 

Propanol with magnesium in reduction of chlorobenzene, 47, 104 Propionyl fluoride, 46, 6 n Propylamine, 46, 85 n Propylhydrazine, 46, 85 C ( Propyl) N phenylmtrone, genera tion from phenylhydroxylamme and n butyraldehyde, 46, 97 Purification of tetrahydrofuran (Warning), 46,105 4H Pyran 4-one, 2 6 dimethyl 3,5 diphenyl, 47, 54... 

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