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H Acetate

Nantokite, see Copper(I) chloride Natron, see Sodium carbonate Naumannite, see Silver selenide Neutral verdigris, see Copper(H) acetate Nitre (niter), see Potassium nitrate Nitric oxide, see Nitrogen(II) oxide Nitrobarite, see Barium nitrate Nitromagnesite, see Magnesium nitrate 6-water Nitroprusside, see Sodium pentacyanonitrosylfer-rate(II) 2-water... [Pg.274]

Sodium ions were removed from the ohgosaccharide fractions hy treatment with Dowex H+. Acetate was evaporated by washing with methanol. [Pg.620]

Write the formula for each of the following compounds (a) hydrogen iodide, (b) calcium chloride, (c) lithium oxide, (d) silver nitrate, (e) iron(II) sulfide, (/) aluminum chloride, (g) ammonium sulfate, (h) zinc carbonate, (/) iron(lll) oxide, ( ) sodium phosphate, (k) iron(H) acetate, (/) ammonium cyanide, and (m) copper(II) chloride. [Pg.110]

Refluxing dipeptide esters in 2-butanol containing 0.1 mol H acetic acid for 3 h. ... [Pg.675]

Betamethasone (Lederie) 1956 R = H, acetate, propionate phosphate, valerate, etc.. [Pg.595]

V-AcetyI-7,9-di-0-acetylneuraminic acid eu5,7,9Ac3 H acetv1 acet 1 H acet> 1... [Pg.135]

Similar treatment of 1.1-spiro compounds leads to different results depending upon the number of atoms in the iro ring. The fivemiembered compound 207 a yields the cyclic 2-oxyphosphinic acid ester 208 a (60%) and only 8% of the 4-hydroxyphosphinic acid ester 209a (R = H). Acetic acid ist not necessary for these transformations. 207b and c (R = D, CH3) react in a similar manner ... [Pg.125]

F,MnO SC6, Manganese( I), pentacarbonyl-(trifluoromethanesulfonato)-, 26 114 F,0 CH, Acetic acid, trifluoro-tungsten complex, 26 222 F,02C,H, Acetic acid, trifluoro-ruthenium complex, 26 254 FjOjSCH, Methanesulfonic acid, trifluoro-iridium, manganese and rhenium complexes, 26 114, 115, 120 platinum complex, 26 126 F304PtSC,4H,5, Platinum(II), hydrido-(methanol)bis(triethylphosphine)-Irans-, trifluoromethanesulfonate,... [Pg.418]

Alternatively, direct electrophilic acylation of a BIPS also occurred in the 3-position. Vilsmeier formylation of 6-nitroBIPS gave 22% of the 3-formyl derivative (113, R=H) acetic anhydride with boron trifluoride etherate in chloroform solvent gave 56% of the 3-acetyl compound (113, R=Me) and benzoyl chloride with aluminium bromide in carbon disulfide solvent gave 26% of 3-benzoyl-6-nitroBIPS (113, R=Ph). None of the 3-acyl BIPS showed any coloration upon UV irradiation in any solvent.106... [Pg.48]

Benzyl esters, ethers and carbamates can be deprotected in the presence of other easily reducible groups by treatment of the substrate with paHadium(H) acetate and triethylamine in the presence of trie thy lsilane.,nR 109 Competing reduction of bromoarenes, cyclopropanes or alkenes is not observed [Scheme 6.43].110... [Pg.396]

Lipase Solvent Time (h) Acetate Yield (%) Optical Purity (% ee)... [Pg.138]

See other pages where H Acetate is mentioned: [Pg.262]    [Pg.41]    [Pg.114]    [Pg.74]    [Pg.240]    [Pg.821]    [Pg.1245]    [Pg.214]    [Pg.4]    [Pg.312]    [Pg.205]    [Pg.130]    [Pg.101]    [Pg.102]    [Pg.1109]    [Pg.180]    [Pg.271]    [Pg.433]    [Pg.98]    [Pg.358]    [Pg.740]    [Pg.149]    [Pg.21]    [Pg.292]    [Pg.324]    [Pg.324]    [Pg.324]    [Pg.496]    [Pg.1033]    [Pg.314]    [Pg.319]    [Pg.137]    [Pg.220]    [Pg.199]    [Pg.196]    [Pg.333]    [Pg.21]    [Pg.476]   


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C«H.O» Acetic anhydride

Ethyl acetate H NMR spectrum

H-Rate profile for release of salicylic acid from benzaldehyde disalicyl acetal

Oxidation of the C-H bond in acetals

Rhodium acetate C—H insertion reactions

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