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1.5 to 3.2 V

5 Iso­propyl 2 methyl 3 phenyl­sulfonyl 1 benzo­furan

5 Iso­propyl 2 methyl 3 phenyl­sulfonyl 1 benzo­furan

... of 5-isopropyl-2- methyl-3-phenylsulfanyl-1-benzofuran (282 mg, ...acetate, 2:1 v/v) to afford the title compound as a colorless solid [yield 81%, ...acetate, ...

8

2 Methyl 3 phenyl­sulfonyl 5 propyl 1 benzo­furan

2 Methyl 3 phenyl­sulfonyl 5 propyl 1 benzo­furan

... 77% 3-Chloroperoxybenzoic acid (471 mg, ...of 2-methyl-3- phenylsulfanyl-5-propyl-1-benzofuran (282 mg, ...acetate, 2:1 v/v) to afford the title compound as ...

8

5 Cyclo­hexyl 2 (2 fluoro­phen­yl) 3 methyl­sulfinyl 1 benzo­furan

5 Cyclo­hexyl 2 (2 fluoro­phen­yl) 3 methyl­sulfinyl 1 benzo­furan

... of 5-cyclo- hexyl-2-(2-fluorophenyl)-3-methylsulfanyl-1-benzofuran (271 mg, ...for 5 h, the mixture was washed with saturated sodium bicarbonate solution and the organic layer ...

8

1 [2 Oxo 1′ phenyl 2′,3′,5′,6′,7′,7a' hexa­hydroindoline 3 spiro 3′ 1′H pyrrolizin 2′ yl] 3 phenyl­prop 2 en 1 one

1 [2 Oxo 1′ phenyl 2′,3′,5′,6′,7′,7a' hexa­hydroindoline 3 spiro 3′ 1′H pyrrolizin 2′ yl] 3 phenyl­prop 2 en 1 one

... A solution of (1E,6E)-4-benzylidene-1,7-diphenylhepta-1,6-diene-3,5-dione (1 mmol), isatin (1 mmol) and L-proline (1 mmol) in aqueous methanol (20 ml) was refluxed until the disappearance of starting ...

11

5 Ethyl 3 (3 fluoro­phenyl­sulfon­yl) 2 methyl 1 benzo­furan

5 Ethyl 3 (3 fluoro­phenyl­sulfon­yl) 2 methyl 1 benzo­furan

... 77% 3-Chloroperoxybenzoic acid (560 mg, ...of 5-ethyl-3-(3- fluorophenylsulfanyl)-2-methyl-1-benzofuran (320 mg, ...4:1 v/v) to afford the title compound as ...

9

5 Cyclo­hexyl 3 (3 fluoro­phenyl­sulfon­yl) 2 methyl 1 benzo­furan

5 Cyclo­hexyl 3 (3 fluoro­phenyl­sulfon­yl) 2 methyl 1 benzo­furan

... 77% 3-chloroperoxybenzoic acid (515 mg, ...of 5-cyclo- hexyl-3-(3-fluorophenylsulfanyl)-2-methyl-1-benzofuran (374 mg, ...4:1 v/v) to afford the title ...

9

3 Ethyl­sulfinyl 2 (3 fluoro­phen­yl) 5 phenyl 1 benzo­furan

3 Ethyl­sulfinyl 2 (3 fluoro­phen­yl) 5 phenyl 1 benzo­furan

... of 3-ethyl- sulfanyl-2-(3-fluorophenyl)-5-phenyl-1-benzofuran (278 mg, ...acetate, 2:1 v/v) to afford the title compound as a colorless solid [yield 62%, ...

9

5 Cyclo­hexyl 3 ethyl­sulfinyl 2 (3 fluoro­phen­yl) 1 benzo­furan

5 Cyclo­hexyl 3 ethyl­sulfinyl 2 (3 fluoro­phen­yl) 1 benzo­furan

... of 5-cyclo- hexyl-3-ethylsulfanyl-2-(3-fluorophenyl)-1-benzofuran (283 mg, ...acetate, 2:1 v/v) to afford the title compound as a colourless solid [yield ...

8

5 Bromo 2 methyl 3 (3 methyl­phenyl­sulfin­yl) 1 benzo­furan

5 Bromo 2 methyl 3 (3 methyl­phenyl­sulfin­yl) 1 benzo­furan

... of 5-bromo-2- methyl-3-(3-methylphenylsulfanyl)-1-benzofuran (300 mg, ...acetate, 2:1 v/v) to afford the title compound as a colorless solid [Yield 78%, ...

8

5 Cyclo­hexyl 2 methyl 3 (3 methyl­phenyl­sulfon­yl) 1 benzo­furan

5 Cyclo­hexyl 2 methyl 3 (3 methyl­phenyl­sulfon­yl) 1 benzo­furan

... of 5-cyclo- hexyl-2-methyl-3-(3-methylphenylsulfanyl)-1-benzofuran (302 mg, ...4:1 v/v) to afford the title compound as a colorless solid [yield 73%, ...

9

5 (p Tolylsulfon­yl) 3 oxa 5 aza­tri­cyclo­[5 2 1 04,8]deca­ne

5 (p Tolylsulfon­yl) 3 oxa 5 aza­tri­cyclo­[5 2 1 04,8]deca­ne

... crude product was purified by flash column chromatography (silica gel; hexane–EtOAc 1:5 v/v) to give 55.6 mg (58%) of the title compound, which was recrystallized from EtOH for X-ray analysis. ...

7

5 Fluoro 2 methyl 3 (3 methyl­phenyl­sulfon­yl) 1 benzo­furan

5 Fluoro 2 methyl 3 (3 methyl­phenyl­sulfon­yl) 1 benzo­furan

... of 5-fluoro-2- methyl-3-(3-methylphenylsulfanyl)-1-benzofuran (245 mg, ...4:1 v/v) to afford the title compound as a colorless solid [yield 71%, ...acetate, ...

8

5 Chloro 3 ethyl­sulfinyl 2 (3 fluoro­phen­yl) 1 benzo­furan

5 Chloro 3 ethyl­sulfinyl 2 (3 fluoro­phen­yl) 1 benzo­furan

... of 5-chloro-3- ethylsulfanyl-2-(3-fluorophenyl)-1-benzofuran (337 mg, ...acetate, 2:1 v/v) to afford the title compound as a colorless solid [yield 67%, ...

10

5 Cyclo­hexyl 2 methyl 3 (3 methyl­phenyl­sulfin­yl) 1 benzo­furan

5 Cyclo­hexyl 2 methyl 3 (3 methyl­phenyl­sulfin­yl) 1 benzo­furan

... of 5-cyclo- hexyl-2-methyl-3-(3-methylphenylsulfanyl)-1-benzofuran (302 mg, ...acetate, 2:1 v/v) to afford the title compound as a colorless solid [yield ...

9

5 Chloro 2 methyl 3 phenyl­sulfonyl 1 benzo­furan

5 Chloro 2 methyl 3 phenyl­sulfonyl 1 benzo­furan

... 77% 3-chloroperoxybenzoic acid (471 mg, ...of 5-chloro-2- methyl-3-phenylsulfanyl-1-benzofuran (275 mg, ...(hexane–ethylacetate, 2:1 v/v) to afford the I as ...

10

An econometric analysis of the Australian Country Party, 1922-1928

An econometric analysis of the Australian Country Party, 1922-1928

... The electoral support of the Nationalist Party and of the Australian Labor Party changed little between 1922 and 1925. Occupational and religious (not economic) variables continued to underlay these parties’ electoral ...

209

tert Butyl 3 oxo 2 oxa 5 aza­bi­cyclo­[2 2 1]heptane 5 carboxyl­ate

tert Butyl 3 oxo 2 oxa 5 aza­bi­cyclo­[2 2 1]heptane 5 carboxyl­ate

... O2 0.0234 (14) 0.0253 (16) 0.0352 (16) 0.0018 (13) 0.0050 (12) −0.0054 (13) O3 0.0253 (15) 0.0189 (14) 0.0349 (16) −0.0018 (13) 0.0067 (12) 0.0007 (13) O4 0.0344 (17) 0.0263 (16) 0.0359 (16) −0.0089 (14) 0.0091 (13) ...

6

Ethyl 2 [5 (4 fluoro­phen­yl)pyridin 3 yl] 1 [3 (2 oxopyrrolidin 1 yl)prop­yl] 1H benzimidazole 5 carboxyl­ate

Ethyl 2 [5 (4 fluoro­phen­yl)pyridin 3 yl] 1 [3 (2 oxopyrrolidin 1 yl)prop­yl] 1H benzimidazole 5 carboxyl­ate

... Ethyl 3-amino-4-(3-(2-oxopyrrolidin-1-yl)propylamino)benzoate ...of 5-(4- fluorophenyl)nicotinaldehyde ...Na 2 SO 4 and the evaporated in vacuo to yield the ...

12

3 (2 Bromo­phenyl­sulfon­yl) 5 cyclo­hexyl 2 methyl 1 benzo­furan

3 (2 Bromo­phenyl­sulfon­yl) 5 cyclo­hexyl 2 methyl 1 benzo­furan

... 3-Chloroperoxybenzoic acid (77%, 426 mg, 1.9 mmol) was added in small portions to a stirred solution of 3-(2-bromo- phenylsulfanyl)-5-cyclohexyl-2-methyl-1-benzofuran (361 mg, ...

9

3,3,4,4,5,5 Hexa­fluoro 1 [2 methyl 5 (2 fluoro­phen­yl) 3 thien­yl] 2 (2 methyl 5 phenyl 3 thien­yl)cyclo­pent 1 ene, a new photochromic dithienylethene

3,3,4,4,5,5 Hexa­fluoro 1 [2 methyl 5 (2 fluoro­phen­yl) 3 thien­yl] 2 (2 methyl 5 phenyl 3 thien­yl)cyclo­pent 1 ene, a new photochromic dithienylethene

... photochromic dithienylethene with an ortho-fluorophenyl substituent, is one of the most promising candidates for photoelectronic applications, such as optical storage, photo- switches and waveguides. There are two ...

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