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Methyl 4,6-0- hydrolysis

Diazaspiro[2.5]octane, 1 -methyl-hydrolysis rate constant, 7, 216 (62CB1759)... [Pg.14]

Diaziridine, 1-cyclohexyl-hydrolysis rate constant, 7, 216 (62CB1759) Diaziridine, 1 -cyclohexyl-3,3-dimethyl-hydrolysis rate constant, 7, 216 (62CB1759) Diaziridine, l-cyclohexyl-3-methyl-hydrolysis rate constant, 7, 216 (62CB1759) Diaziridine, l,2-di-t-butyl-3-t-butylimino-IR, 7, 13 <80AG(E)276)... [Pg.14]

Imidazo[ 1,5-a]pyrazine, 1 -bromo-3-methyl-hydrolysis, S, 625 reactivity, 5, 625... [Pg.660]

Pteridine-2,7-dione, 4-amino-8-benzyl-6-methyl-hydrolysis, 3, 294... [Pg.753]

Pteridine-2,4,7-trione, 8-benzyl-6-methyl-hydrolysis, 3, 294 Pteridine-2,4,7-trione, 1-methyl-reactions, 3, 296 Pteridine-2,4,7-trione, 3-methyl-reactions, 3, 296 Pteridine-2,6,7-trione, 4-amino-chlorination, 3, 296 Pteridinetriones structure, 3, 272... [Pg.755]

Pterin, 6-hydroxymethyl-7,7-dimethyl-7,8-dihydro-bacteriostatic activity, 3, 325 Pterin, 1-methyl-hydrolysis, 3, 294 5-oxide... [Pg.756]

NMR, 5, 513 UV spectra, 5, 517 Purine, 8-methoxy-UV spectra, 5, 517 Purine, 6-methoxy-3-methyl-hydrolysis, 5, 558 irradiation, 5, 543... [Pg.759]

Purine, 6-methoxy-9-methyl-hydrolysis, 5, 558 Purine, 1-methyl- H NMR, 5, 511 synthesis, 5, 594 Purine, 2-methyl-amination, 5, 542 mass spectra, 5, 519 synthesis, 5, 593 Purine, 3-methyl- H NMR, 5, 511 occurrence, 5, 598 synthesis, 5, 586, 595 Purine, 6-methyl-amination, 5, 542 mass spectra, 5, 519 methylation, 5, 529 oxidation, 5, 539 1-oxide... [Pg.759]

Pyrimidin-2-amine, 4-ethyI-5-(2 -hydroxy-4 -nitrophenyI)-6-methyl-synthesis, 3, 121 Pyrimidin-2-amine, 4-methyl-basic pXj, 3, 61 Pyrimidin-2-amine, N-methyl-hydrolysis, 3, 84 synthesis, 3, 135 Pyrimidin-2-amine, 5-nitro-basic pXj, 3, 61 hydrolysis, 3, 84 Pyrimidin-2-amine, 4-phenyl-synthesis, 3, 109 Pyrimidin-2-amine, 5-phenyl-nitration, 3, 78... [Pg.802]

Recovery of acetic acid and methanol from methyl Hydrolysis... [Pg.1320]

Similar products (but having R = /3-D-galactopyranosyl) were obtained from octa-O-acetyllactobiononitrile56 in 25% aqueous ammonia. The furanose structure of the monoamido derivative 61 (and that of its analog N-acetyl-3-0-/3-D-galactopyranosyl-D-arabinofuranosyl-amine56) was ascertained by methylation, hydrolysis, and identification of 2,5-di-O-methyl-D-arabinose. [Pg.98]

Purine, 6-iodo-alkylation, 5, 530 synthesis, 5, 563, 597 Purine, 6-iodo-9-/3-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 NMR, 5, 513 UV spectra, 5, 517 Purine, 8-methoxy-UV spectra, 5, 517 Purine, 6-methoxy-3-methyl-hydrolysis, 5, 558 irradiation, 5, 543... [Pg.759]

Pyrimidine-4,5-dicarbonitrile, 2-methyl-hydrolysis, 3, 83, 84 Pyrimidine-4,5-dicarboxylic acid synthesis, 3, 76, 122 Pyrimidine-4,6-dicarboxylic acid decarboxylation, 3, 80... [Pg.807]

Conclusive proof of the structures of the glycosides B and C was obtained by methylation, hydrolysis, oxidation and comparison of the rates of hydrolysis of the lactones so obtained. From the glycoside B a 1,5-lactone was obtained,141 whereas a 1,4-lactone was derived from C, showing that the glycoside B had a 1,5-pyranose lactol ring and C a 1,4-furanose lactol ring. Since A and B were a- and /3-anomers, it followed that A also had a pyranose structure. [Pg.96]

The proof of structure of D-galactosana was based on methylation, hydrolysis of the trimethyl-D-galactosan, and characterization of the trimethyl-D-galactose thus obtained. Both 2,4,6-tri-methyl-D-galactose13 and 2,3,5-trimethyl-D-galactoseu had been reported in the literature and provided a sound basis for a choice between the <1,5> <1,3> and the <1,4> <1,6> ring systems. [Pg.43]

D-Ribose reacts rapidly at room temperature with methanol containing 1 % of hydrogen chloride, and methyl D-ribofuranoside, which may be purified by vacuum distillation, is the initial product.89 The structure of the compound was shown through methylation, hydrolysis and oxidation to 2,3,5-trimethyl-D-ribonolactone, which hydrolyzed in water at a rate characteristic of y-lactones. [Pg.159]


See other pages where Methyl 4,6-0- hydrolysis is mentioned: [Pg.567]    [Pg.608]    [Pg.714]    [Pg.724]    [Pg.806]    [Pg.809]    [Pg.835]    [Pg.843]    [Pg.231]    [Pg.206]    [Pg.505]    [Pg.608]    [Pg.714]    [Pg.724]    [Pg.806]    [Pg.809]    [Pg.835]    [Pg.843]    [Pg.1136]    [Pg.263]    [Pg.590]   
See also in sourсe #XX -- [ Pg.40 , Pg.71 , Pg.72 , Pg.75 , Pg.77 , Pg.78 , Pg.80 , Pg.81 , Pg.106 , Pg.107 , Pg.108 , Pg.109 , Pg.115 , Pg.116 , Pg.168 , Pg.169 , Pg.170 , Pg.176 , Pg.177 ]

See also in sourсe #XX -- [ Pg.22 , Pg.31 ]




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3-methyl-4-nitro-phenyl ester hydrolysis

Acid hydrolysis of methyl

Glycine methyl ester, hydrolysi

Hydrolysis methylated material

Hydrolysis neutral methylated polysaccharides

Hydrolysis of Methyl Acetate in Acidic Media

Hydrolysis of a methyl ester

Hydrolysis of methyl acetate

Hydrolysis of methyl chlorides

Hydrolysis of methyl ester

Hydrolysis of methylated

Hydrolysis of methylated polysaccharides

Hydrolysis of racemic naproxen methyl

Hydrolysis products of methylated

Mannans hydrolysis products from methylated

Methionine methyl ester hydrolysis

Methyl 2 methylpropenoate hydrolysis

Methyl 2-hydroxy benzoate, hydrolysis

Methyl 2-pyrazinecarboxylate hydrolysis

Methyl 3,4-0-benzylidene hydrolysis

Methyl acetate, hydrolysis

Methyl benzoate, hydrolysis

Methyl benzoate, hydrolysis preparation

Methyl benzoates, alkaline hydrolysis

Methyl bromide, hydrolysis

Methyl bromide, hydrolysis reaction with pyridine

Methyl chloride hydrolysis

Methyl chloroformate, hydrolysis

Methyl cyclohexenyl ether, hydrolysis

Methyl ester acid hydrolysis

Methyl ester hydrolysis, selectivity

Methyl ethylene phosphate, hydrolysis

Methyl formate, hydrolysis

Methyl glycinate, hydrolysis

Methyl halides, hydrolysis

Methyl hydrogen succinate, hydrolysis

Methyl naphthoates, hydrolysis

Methyl nitrobenzoates, hydrolysis

Methyl octanoate, hydrolysis

Methyl orthobenzoate hydrolysis

Methyl orthobenzoates, hydrolysis

Methyl oxalate, reactions hydrolysis

Methyl parathion hydrolysis

Methyl phosphate, hydrolysis

Methyl phthalate, hydrolysis

Methyl propionate, alkaline hydrolysis

Methyl salicylate, hydrolysis

Methyl trichloroacetate, hydrolysis

Methyl trifluoroacetate, hydrolysis

Methylation in hydrolysis of dithiane

Oligosaccharide methylated, hydrolysis

Polysaccharides methylated, hydrolysis

Polysaccharides methylated, partial acid hydrolysis

Thermally assisted hydrolysis and methylation

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