2- Methoxy-2,4-diphenyl-3

Bis-[trifluormethy]]-2,2-diphenyl-2-methoxy-(4-methyl-phenyl)-2,3-dihydro- E2, 873... 

Ethanamme, 2-(diphenylmethoxy)-jV,vV-di-methyl- [Ethylamine, (2-diphenyl-methoxy)-A,Ar-dimethyl-, Diphenhydramine], 55, 3, 4... 

Methane, diphenyl methoxy [Ether, di phenylmethyl methyl], 55, 5 Metharte, iodo-, 55, 3 METHANE, iodo-, hazard note, 55, 134 Methane, (4 (l-methylethvl)phenyl)-phenyl-[Melliane, (4-isopropylphenyl)-phen-yl-], 55,11... 

Z)-2-amIno- -(2-diphenyl-methoxy-1.1 -dlmethyl-2-oxo-ethoxyimino)-4-thia2ole-ocetic odd (VIII)... 

CjpHujNO, 128289-78-1) see Moexipril [6R-[6a,7p(lf )]]-7-[[5-(benzoylamino)-6-(diphenyl-methoxy)-l,6-dioxohexyl]amino]-3-(chloromethyl)-8-oxo-5-thia-l-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester (C47H42CIN3O7S) see Cefixime [6fi-[6a,7P(R )]]-7-[[5-(benzoyIamino)-6-(diphenyl-methoxy)-l,6-dioxohexyl]amino]-3 -ethenyl-8-oxo-5-thia-... 

Ebenso fiihrt die Umsetzung von Diazomethan mit (Bis-[phenylsulfonyl]-methyl)-diphe-nyl-phosphanoxid zu (Bis-[phenylsulfonyl]-methylen)-diphenyl-methoxy-phosphoran460 ... 

Arbeitsvorschrift Zur Ldsung der Hexafluoraceton-benzoylimine in wasserfreiem Hexan wird bei 0° die aqui-molare Menge Diphenyl-methoxy-phosphoran gctropft. Man laBt mehrcre Stunden bei 0° stehcn, trennt das aus-gefallene Produkt ab und kristallisiert aus Hexan. 

Diphenyl-(l-mcthoxy-3-phenyl-allyl)- E2, 14 Diphcnyl-(2-methoxy-propyl)- E2, 14 Diphenyl-(5-methoxy-2-tctrahydrofuryl)- E2, 14 Diphenyl-methyl- XI1/1, 137, 142, 148, 150, 152, 238 E2, 16, 34, 42, 64, 148 aus Diphenyl-methoxy-phosphan und Azo-methan (Belichtung) E2, 26 aus Triphenyl-phosphan und Dimethylsulfat XII/1, 145... 

Diphenyl-(1-phenyl-propyl)- E2, 147 Diphenyl-(2-phcnyl-vinyl)- E2, 66 Diphenyl-[2-(/ranv-2-phcnyl-vinyl)-phenyl)-aus Diphenyl-(2-phenyl-ethinyl)-phosphan und wasserhaltigem Ethanol E2, 48 Diphenyl-(phthalimino-methyl)- E2, 22 Diphenyl-piperidinomethyl- XII/1, 155 Diphenyl-1-propinyl- E2, 76 Diphenyl-tosyloxymethyl- El, 513 Diphenyl-(3-trialkylsik>xy-a]]yD- E2, 27 Diphenyl-trichlormethyl- XII/1, 151 F.2, 23 (Z)-Diphenyl-(3-triethylsilyloxy-allyl)- E2, 27 (Z)-Diphenyl-(3-triethylsilyloxy-2-butenyl)-aus Diphenyl-methoxy-phosphan und Chlor-triethyl-silan/3-Oxo-l-butcn E2, 27 Diphenyl-trifluoracctyl- E2, 8, 19, 42 Diphenyl-(2,2,2-lrifluor-ethyl)- E2, 16 Diphenyl-(l,l,3-trimethyl-2-butenyl)- E2, 71 Diphenyl-(trimethylsilyl-methyl)- E2, 22, 66 Diphcnyl-(l-trimethylsilyloxy-alkyl)- E2, 26 Diphenyl-triphenylmethyl-XlI/1,151 Diphenyl-(triphenylstannyl-methyl)-... 

Diphenyl-methoxy- (tetrafluoro-borat) Ell, 369 (O-Alkylier.) (4-Hydroxy-phenyl)-methyl-phenyl-(pikrat) Ell, 470 (R2SO + ArH)... 

Bis-[dicyano-melhylene]-cyclo-propyl)-bis-[dimethylamino]-3110 C H,30 Cyclopropenylium Diphenyl-methoxy- 3185. 3186 C H.jS Cyclopropenylium Uiphenyl-melhylthio- 272b. 272S. 2729.3052. 3083,3108,3123.3154, 3166-3168. 3172... 

Ether, diphenylmethyl methyl [Methane, diphenyl-methoxy-], 55, 5 ETHER, diphenylmethyl vinyl [Benzene,... 

Tis((9-propenylphenoxy)diphenyl sulfone. 4,4 Bis(o-methoxy-/)-propenylphenoxy)diphenyl sulfone. 4,4Tis ((9-propen5lphenoxy)benzophenone. 

There is a scattered body of data in the literature on ordinary photochemical reactions in the pyrimidine and quinazoline series in most cases the mechanisms are unclear. For example, UV irradiation of 4-aminopyrimidine-5-carbonitrile (109 R=H) in methanolic hydrogen chloride gives the 2,6-dimethyl derivative (109 R = Me) in good yield the 5-aminomethyl analogue is made similarly (68T5861). Another random example is the irradiation of 4,6-diphenylpyrimidine 1-oxide in methanol to give 2-methoxy-4,6-diphenyl-pyrimidine, probably by addition of methanol to an intermediate oxaziridine (110) followed by dehydration (76JCS(P1)1202). 

After the initial claim of the synthesis of an oxirene (by the oxidation of propyne Section 5.05.6.3.1) this system reappeared with the claim 31LA(490)20l) that 2-chloro-l,2-diphenyl-ethanone (110) reacted with sodium methoxide to give diphenyloxirene (111), but it was later shown (52JA2082) that the product was the prosaic methoxy ketone (112 Scheme 97) (the formation of 111 from 110 would be an a-elimination carbene-type reaction). Even with strong, nonnucleophilic bases, (110) failed to provide evidence of diphenyloxirene formation (64JA4866). 

C NMR, 7, 498 (79TH51600) 2H-Azepine-4-carboxylic acid, 7-(4-bromophenyl)-3-methoxy-2-oxo-6-phenyl-X-ray, 7, 494 <79H(12)1423> 3H-A2epine-4-carboxylic acid, 6-acetyl-2-ethoxy-3-oxo-7-phenyl-, ethyl ester H NMR, 7, 503 <81H(16)363) 3H-Azepine-4-carboxylic acid, 2,6-diethoxy-3-oxo-7-phenyl-, ethyl ester H NMR, 7, 503 <81H(16)363) 3H-Azepine-4-carboxylic acid, 2-ethoxy-3-oxo-6,7-diphenyl-, ethyl ester HNMR, 7, 503 <81H(16)363) 3H-Azepine-4-carboxylic acid, 2-ethoxy-3-oxo-7-phenyl-, ethyl ester... 

Aziridine, 2,3-diphenyl-l-(2,4,6-trinitrophenyl)-irradiation, 7, 61 Aziridine, 1,2-divinyl-rearrangement, 7, 539 Aziridine, 2,3-divinyl-rearrangement, 7, 42, 65, 539 Aziridine, N-ethyl-inversion, 7, 6 Aziridine, 2-halo-reactions, 7, 74 Aziridine, A/-halo-invertomers, 7, 6 Aziridine, 2-methyl- N NMR, 7, 11 Aziridine, methylene-ring-ring valence isomerizations, 7, 22 synthesis, 7, 92 Aziridine, iV-nitroso-reactions, 7, 74 Aziridine, iV-phosphino-inversion, 7, 7 Aziridine, 1-phthalimido-UV irradiation, 7, 62-63 Aziridine, l-(3-thienyl)-2-vinyl-rearrangement, 4, 746 Aziridine, 7V-trimethylsilyl-inversion, 7, 7 Aziridine, 1,2,3-triphenyl-irradiation, 7, 61 Aziridine, vinyl-isomerization, S, 287 Aziridinecarboxylic acid ring expansion, 7, 262 Aziridine-2,2-dicarboxylic acid, 1-methoxy-diethyl ester... 

Benzo[b]furan, 3-(2-hydroxy-3,5-dichlorophenyl)-5,7-dichloro-properties, 4, 708 Benzo[b]furan, 2-lithio-synthesis, 4, 652 Benzo[i]furan, 3-lithio-ring opening, 4, 79 Benzo[b]furan, methoxy-mass spectrometry, 4, 583 Benzo[b]furan, 6-methoxy-2,3-diphenyl-synthesis, 4, 679... 

Lithium, l,3-(cw, trani)-diphenyl-2-azaallyl-generation, 7, 73 Lithium, 5-iodo-2-thienyI-synthesis, 4, 831 Lithium, 2-methoxy-4-furyl-... 

H-Pyran, 2-alkoxy-4-methyl-2,3-dihydro-conformation, 3, 630 4H-Pyran, 2-amino-IR spectra, 3, 593 synthesis, 3, 758 4H-Pyran, 4-benzylidene-synthesis, 3, 762 4H-Pyran, 2,3-dihydro-halogenation, 3, 723 hydroboration, 3, 723 oxepines from, 3, 725 oxidation, 3, 724 reactions, with acids, 3, 723 with carbenes, 3, 725 4H-Pyran, 5,6-dihydro-synthesis, 2, 91 4H-Pyran, 2,6-diphenyl-hydrogenation, 3, 777 4H-Pyran, 6-ethyl-3-vinyl-2,3-dihydro-reactions, with acids, 3, 723 4H-Pyran, 2-methoxy-synthesis, 3, 762 4H-Pyran, 2,4,4,6-tetramethyl-IR spectra, 3, 593 4H-Pyran, 2,4,6-triphenyl-IR spectra, 3, 593... 

Pyran-4-one, 2,6-bis(diethylamino)-3,5-diphenyl-conformation, 3, 622 Pyran-4-one, 2-chloromethyl-5-methoxy-benzothiazoles from, 3, 713 Pyran-4-one, 3,5-diacyl-IR spectra, 3, 595 Pyran-4-one, 3,5-dibenzyl-IR spectra, 3, 595... 

Selenophene, 2,5-dimethyl-3-mercapto-synthesis, 4, 956 tautomerism, 4, 946 Selenophene, 2,4-diphenyl-synthesis, 4, 135 Selenophene, 2,5-diphenyl-lithiation, 4, 949 UV spectra, 4, 941 Selenophene, 2-ethoxycarbonyl-mercuration, 4, 946 Selenophene, halo-reactions, 4, 955 Selenophene, 2-hydroxy-Michael reaction, 4, 953 tautomerism, 4, 36, 945, 953 Selenophene, 3-hydroxy-tautomerism, 4, 36, 945 Selenophene, 3-hydroxy-2,5-dimethyl-tautomerism, 4, 945, 953 Selenophene, 2-hydroxy-5-methyl-methylation, 4, 953 tautomerism, 4, 945 Selenophene, 2-hydroxy-5-methylthio-tautomerism, 4, 945 Selenophene, 3-iodo-synthesis, 4, 955 Selenophene, 3-lithio-reactions, 4, 79 synthesis, 4, 955 Selenophene, 2-mercapto-tautomerism, 4, 38 Selenophene, 3-mercapto-tautomerism, 4, 38 Selenophene, 2-mercapto-5-methyl-synthesis, 4, 956 tautomerism, 4, 946 Selenophene, 3-methoxy-lithiation, 4, 949, 955 synthesis, 4, 955 Selenophene, methyl-oxidation, 4, 951 synthesis, 4, 963 Selenophene, 2-methyl-lithiation, 4, 949 Selenophene, 3-methyl-synthesis, 4, 963... 

Yields of 54% of 2-methoxy-4 -methyl diphenyl ether from -bromotoluene and guaiacol, and 60% of 2-mcthoxy-5-methyl-diphenyl ether from 3-bromo-4-methoxytoluene and phenol, have been obtained by the same method in the laboratory of the submitters,... 

Dipping solution Dissolve 25 mg 2-methoxy-2,4-diphenyl-3(2H)-furanone in 50 ml methanol. 

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