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Tartartic acid

Acetylene, oxalic acid, tartartic acid, ammonium compounds, fulminic acid... [Pg.262]

Acetylene, oxalic acid, tartartic acid, ammonium compounds, fulminic acid Carbon tetrachloride, carbon dioxide, water Ammonium nitrate and other ammonium salts... [Pg.2366]

A Figure 16.1 Two oiganic acids Tartartic acid, >12641140, and malic acid, H2C4K4O5. [Pg.672]

Analogously, PRC has been exploited to selectively epimerize carbon centers of the t)rpe R R C(H)OR, for example, to convert a readily available carbohydrate-based diastereoisomer into a rarer one, and in ring opening of acetals to benzoate esters (eq 9) shows the conversion of a derivative of natural (i ,i )-tartartic acid into that of unnatural (T -malic acid. [Pg.271]

Racemic A,A -dimethyl-l,2-diphenylethylenediamine was treated with L-(+)-tartaric acid to afford a pair of diastereomeric salts which were separated overnight by selective precipitation from ethanol. The (R,R)-diamine was separated by filtration, followed by extraction with base to remove the tartartic acid. Removal of the solvent produced the crude diamine in 90% yield and greater than 99% ee. The (5,5)-diamine was isolated by concentration of the mother liquor and the same extraction procedure to... [Pg.45]

The first example of catalytic, enantioselective Sakurai reaction was effected by means of Yamamoto s chiral acyloxyborane (CAB) catalyst 96 (Table 11). The CAB catalysts are derived from tartartic acid, and 97 gave a better yield than 96. ... [Pg.557]


See other pages where Tartartic acid is mentioned: [Pg.184]    [Pg.185]    [Pg.184]    [Pg.185]    [Pg.157]    [Pg.184]    [Pg.185]    [Pg.184]    [Pg.185]    [Pg.157]   


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