4-iodo-1-methoxy

III-G-50. Iodo(methoxy)methane (lodomethyl Methyl Ether,... [Pg.499]

Imidazole, 1 -hydroxy-2,4,5-triphenyl-3-oxides reactions, S, 455 Imidazole, iodo-nitrodehalogenation, 5, 396-397 Imidazole, 1-iodo-reactions, S, 454 stability, S, 110 Imidazole, 2-iodo-synthesis, S, 401 Imidazole, N-iodo-, S, 393 reactions, 5, 454 Imidazole, 4-iodo-5-methyl-iodination, 5, 400 Imidazole, 2-isopropyl-4-nitro-N-nitration, 5, 351 Imidazole, 2-lithio-reactions, S, 106, 448 Imidazole, 2-mercapto-l-methyl-as antithyroid drug, 1, 171 mass spectra, 5, 358 Imidazole, 1-methoxymethyl-acylation, S, 402 Imidazole, 5-methoxy-l-methyl-reactions... [Pg.652]

Indazole, 5,5-dimethyl-3-trifluoromethyl-4,5-dihydro-trichomonacidal activity, 5, 291 Indazole, 2-ethoxycarbonyl-reactions, 5, 269 Indazole, 3-fluoro-synthesis, S, 263 Indazole, 1-germyl-synthesis, 5, 236 Indazole, 1-glycosyl-synthesis, 5, 289 Indazole, 2-glycosyl-synthesis, 5, 289 Indazole, halo-reactions, S, 266 Indazole, 2-hydroxy-methylation, 5, 269 Indazole, 3-hydroxy-reactions, S, 264 Indazole, 6-hydroxy-diazo coupling, 5, 86 Indazole, hydroxyphenyl-synthesis, S, 288 Indazole, 3-iodo-synthesis, S, 241 Indazole, l-isopropyl-3-phenyl-reduction, 5, 243 Indazole, 3-mercapto-1 -substituted tautomerism, 5, 265 Indazole, methoxy-... [Pg.664]

Indole, 3-hydroxymethyl-2-phenyl-stability, 4, 272 Indole, I-hydroxy-2-phenyl-synthesis, 4, 363 Indole, 2-iodo-synthesis, 4, 216 Indole, 3-iodo-reaetions, 4, 307 synthesis, 4, 216 Indole, 2-iodo-l-methyl-reaetions, 4, 307 Indole, 2-lithio-synthesis, 4, 308 Indole, 3-lithio-synthesis, 4, 308 Indole, 2-mereapto-tautomerism, 4, 38, 199 Indole, 3-mercapto-tautomerism, 4, 38, 199 Indole, 3-methoxy-synthesis, 4, 367 Indole, 5-methoxy-oxidation, 4, 248 Indole, 7-methoxy-2,3-dimethyl-aeetylation, 4, 219 benzoylation, 4, 219 Indole, 5-methoxy-l-methyl-reduetion, 4, 256 Indole, 5-methoxy-l-methyl-3-(2-dimethylaminoethyl)-reaetions... [Pg.668]

Lithium, l,3-(cw, trani)-diphenyl-2-azaallyl-generation, 7, 73 Lithium, 5-iodo-2-thienyI-synthesis, 4, 831 Lithium, 2-methoxy-4-furyl-... [Pg.697]

Purine, 6-iodo-alkylation, 5, 530 synthesis, 5, 563, 597 Purine, 6-iodo-9- -D-(2,3,5-tri-0-acetyl)ribofuranosyl-synthesis, 5, 598 Purine, 9-isopropyl-deuterium-hydrogen exchange, 5, 527 Purine, 9-(2,3-0-isopropylidene-/3-D-ribofuranosyl)-6-methoxy-synthesis, 5, 584 Purine, 6-mercapto-biological activity, 5, 604 metabolism, 1, 237 as pharmaceutical, 1, 159 tautomerism, 5, 509 Purine, 2-methoxy-synthesis, 5, 596 Purine, 6-methoxy-irradiation, 5, 543 riboside... [Pg.759]

Pyrazole, 5-hydroxy-3-methyl-l-phenyl-4-[(o-tolylazo)]-as dyestuff, 5, 299 Pyrazole, 4-iodo-synthesis, 5, 241 Pyrazole, IV-iodo-reactions, 5, 270 synthesis, 5, 234 Pyrazole, 5-mercapto-tautomerism, 5, 265 Pyrazole, methoxy-pharmaceutical activity, 5, 294 reactions... [Pg.772]

Pyridinium salts, 3-iodo-l-methyl-covalent amination, 2, 239 Pyridinium salts, 1-methoxy-covalent amination, 2, 239 nitration, 2, 188 reactions... [Pg.795]

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... [Pg.841]

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... [Pg.148]

C7H4IO2 88-67-5) see Chlorprothixene laS-laR (l , 3S ),p/f, 8S ]]-a-(4-iodo-l-methoxy-3-methylbutyl)-P-niethoxy-g-methyl-l,3-dithiane-2-butanol (C, .H7 IOjS2 118246-96 ) see Tacrolimus... [Pg.2402]

Compare the structures of 3-methoxy-3-methylpentane and 3-iodo-3-methylpentane, and identify which compound is more likely to undergo an SnI reaction. [Pg.220]

Bromoanisole Anisole, p-bromo- (8) Benzene, 1-bromo-4-methoxy- (9) (104-92-7) Methyl iodide Methane, iodo- (8,9) (74-88-4)... [Pg.54]

The reaction of phenyl-1,2-propadiene with iodine bromide in MeOH afforded a 100% yield of 2-iodo-3-phenyl-3-methoxy-l-propene whereas the reaction in CS2 at 0°C provided a l 4mixture of 2-iodo-3-phenyl-3-bromo-l-propene and l-phenyl-2-iodo-3-bromo-l-propene [16]. The corresponding chlorination shows a lower regios-... [Pg.599]

The reaction of 2,3-pentadiene with I2 in MeOH afforded a 9 1 Z E ratio of 3-iodo-4-methoxy-2-pentene [17]. [Pg.599]

The Suzuki coupling of 2-iodo-2-cyclohexen-1-one and 4-methoxy-phenylboronic acid is achieved using silver(l) oxide as a suspension in aqueous THF as the base. Unlike earlier reports,15-17 in which up to 6 equiv of Ag2mild conditions, rapid conversion can be achieved at room temperature for a large variety of sensitively functionalized partners in near quantitative yields (see Table).18... [Pg.38]

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