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Synthesis disubstituted

IsoxazoIidine-3,3-dicarboxylic acid, 2-methoxy-dimethyl ester reaction with bases, 6, 47 Isoxazolidine-3,5-diones synthesis, 6, 112, 113 Isoxazoli dines conformation, 6, 10 3,5-disubstituted synthesis, 6, 109 oxidation, 6, 45-46 PE spectra, 6, 5 photolysis, 6, 46 pyrolysis, 6, 46 reactions, 6, 45-47 with acetone, 6, 47 with bases, 6, 47 reduction, 6, 45 ring fission, S, 80 spectroscopy, 6, 6 synthesis, 6, 3, 108-112 thermochemistry, 6, 10 Isoxazolidin-3-ol synthesis, 6, 111 Isoxazolidin-5-oI synthesis, 6, 111... [Pg.690]

Isoxazol-3-ol, 5-methyl- — see Hymexazoi Isoxazoi-5-ones 3,4-disubstituted synthesis, 6, 64 5-substituted tautomerism, 6, 11 synthesis, 6, 64 Isoxazolo[2,3-h][ 1,2]oxazines synthesis, 6, 633 Isoxazolophanes... [Pg.692]

Oxepin, 4-ethoxycarbonyl-2,3,6,7-tetrahydro-synthesis, 7, 578 Oxepin, 2-methyl-enthalpy of isomerization, 7, 555 Oxepin, 2,3,4,5-tetrahydro-reduction, 7, 563 synthesis, 7, 578 Oxepin, 2,3,4,7-tetrahydro-synthesis, 7, 578 Oxepin, 2,3,6,7-tetrahydro-oxidation, 7, 563 reduction, 7, 563 Oxepin-2,6-dicarboxylic acid stability, 7, 565 Oxepinium ions synthesis, 7, 559 Oxepins, 7, 547-592 antiaromaticity, 4, 535 applications, 7, 590-591 aromatization, 7, 566 bond lengths and angles, 7, 550, 551 cycloaddition reactions, 7, 27, 569 deoxygenation, 7, 570 dipole moment, 7, 553 disubstituted synthesis, 7, 584... [Pg.732]

Pteridin-6-one, 2-chloro-7,8-dihydro-reduction, 3, 293 Pteridin-6-one, 7,8-dihydro-oxidation, 3, 307 structure, 3, 279 Pteridin-6-one, 7-methyl-2,4-disubstituted synthesis, 3, 310 hydroxylation, 3, 287... [Pg.755]

Pyrimido[5,4-d]pyrimidine, 4-amino-2,8-dihydroxy-3,8-disubstituted synthesis, 3, 365... [Pg.811]

Thiazole, 4-methyl-5-(2-hydroxyethyl)-in thiamine biosynthesis, 1, 97 Thiazole, 4-methyl-2-methylami nosynthesis, 6, 300 Thiazole, 4-methyl-2-phenyl-alkylation, 6, 256 mercuration, 6, 256 Thiazole, 2-(methylthio)-methylation, 6, 290 thermodynamic values, 6, 291 Thiazole, 2-methylthio-5-phenyl-synthesis, 5, 153 Thiazole, 4-methyl-5-vinyl-occurrence, 6, 327 Thiazole, 2-phenyl-acetylation, 6, 270-271 Conformation, 6, 237 synthesis, 5, 113, 6, 306 Thiazole, 4-phenyl-conformation, 6, 237 2,5-disubstituted synthesis, 6, 304 Thiazole, 5-phenyl-conformation, 6, 237 Thiazole, 2-phenyl-5-triphenylmethyl-synthesis, 6, 265 Thiazole, 2-(2-pyridyl)-metal complexes, 5, 51 6, 253 Thiazole, 4-(2-pyridyl)-metal complexes, S, 51 6, 253 Thiazole, tetrahydro-ring cleavage, 5, 80 Thiazole, 2,4,5-trimethyl-occurrence, 6, 327... [Pg.872]

Thiophene, 2,5-dimethyl-3-lithio-ring opening, 4, 81 Thiophene, 2,5-dimethylthio-3,4-disubstituted synthesis, 4, 872 Thiophene, dinitro-... [Pg.891]

Thiophene, 3-methyl-4-phenyl-phototranspositions, 4, 743 Thiophene, 2-(methylthio)-3,4-disubstituted synthesis, 4, 876, 931 Thiophene, nitro-... [Pg.892]

Thiophene-2-carbonitrile, 3-azido-synthesis, 4, 807 Thiophene-2-carboxamide 3,5-disubstituted synthesis, 4, 9l9 5-substituted protonation, 4, 755... [Pg.893]

Diels-Alder reactions, 4, 842 flash vapour phase pyrolysis, 4, 846 reactions with 6-dimethylaminofuKenov, 4, 844 reactions with JV,n-diphenylnitrone, 4, 841 reactions with mesitonitrile oxide, 4, 841 structure, 4, 715, 725 synthesis, 4, 725, 767-769, 930 theoretical methods, 4, 3 tricarbonyl iron complexes, 4, 847 dipole moments, 4, 716 n-directing effect, 4, 44 2,5-disubstituted synthesis, 4, 116-117 from l,3-dithiolylium-4-olates, 6, 826 electrocyclization, 4, 748-750 electron bombardment, 4, 739 electronic deformation, 4, 722-723 electronic structure, 4, 715 electrophilic substitution, 4, 43, 44, 717-719, 751 directing effects, 4, 752-753 fluorescence spectra, 4, 735-736 fluorinated derivatives, 4, 679 H NMR, 4, 731 Friedel-Crafts acylation, 4, 777 with fused six-membered heterocyclic rings, 4, 973-1036 fused small rings structure, 4, 720-721 gas phase UV spectrum, 4, 734 H NMR, 4, 7, 728-731, 939 solvent effects, 4, 730 substituent constants, 4, 731 halo... [Pg.894]

Coumarin, 7-diethylamino-4-methyl-fluorescence, 3, 879 Coumarin, dihydro-chroman synthesis from, 3, 785 4H-chromene synthesis from, 3, 765 coumarin synthesis from, 3, 810 mass spectra, 2, 23 synthesis, 3, 848 Coumarin, 3,4-dihydro-4,4-disubstituted synthesis, 3, 754... [Pg.586]


See other pages where Synthesis disubstituted is mentioned: [Pg.520]    [Pg.569]    [Pg.586]    [Pg.634]    [Pg.634]    [Pg.634]    [Pg.656]    [Pg.656]    [Pg.659]    [Pg.676]    [Pg.677]    [Pg.692]    [Pg.708]    [Pg.716]    [Pg.722]    [Pg.731]    [Pg.790]    [Pg.801]    [Pg.819]    [Pg.819]    [Pg.831]    [Pg.842]    [Pg.855]    [Pg.863]    [Pg.867]    [Pg.871]    [Pg.875]    [Pg.912]    [Pg.520]    [Pg.523]    [Pg.569]    [Pg.610]    [Pg.634]    [Pg.634]    [Pg.634]    [Pg.656]    [Pg.656]    [Pg.656]    [Pg.659]    [Pg.673]   
See also in sourсe #XX -- [ Pg.532 ]




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