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Alkylidene acids

Under phase transfer conditions, nickel can also catalyze double carbonylation of halide substrates. 2-Halo-l,3-dienes have been converted into a-keto-/3-alkylidene acids or lactones catalyzed by nickel cyanide in the presence of a phase transfer agent (Eq. [Pg.767]

The alkylidene dimethone (dimedone) (I) upon boiling with glacial acetic acid, acetic anhydride, hydrochloric acid and other reagents frequently loses water and passes into a substituted octahydroxanthene or the anhydride (II), which often serves as another derivative. The derivatives (I) are soluble in dilute alkali and the resulting solutions give colourations with ferric chloride solution on the other hand, the anhydrides (II) are insoluble in dilute alkali and hence can easily be distinguished from the alkylidene dimedones (I). [Pg.333]

However, benzylidene derivatives show a strong bathochromic shift in comparison with alkylidene derivatives. Thus absorption is a result of the whole conjugated system that is comparable to that of the quinoid dyes. The color of this type of compound is sensitive to acids and bases. [Pg.251]

Butenolide, 2-hydroxy — see Isotetronic acids Butenolide, 3-hydroxy — see Tetronic acids But-2-enolide, 4-alkylidene-synthesis, 4, 697 Butenolides H NMR, 4, 578 mass spectrometry, 4, 585 structure, 4, 551 synthesis, 1, 416 trimethylsilylation... [Pg.572]

Compounds i, ii, and iii can be prepared by an acid-catalyzed reaction of a diol and the cycloalkanone in the presence of ethyl orthoformate and mesitylene-sulfonic acid. The relative ease of acid-catalyzed hydrolysis [0.53 M H2SO4, H2O, PrOH (65 35), 20°] for compounds i, iii, acetonide, and ii is C5 C7 > acetonide C (e.g., t.//s for 1,2-O-alkylidene-a-D-glucopyranoses of C5, C7, acetonide, and C derivatives are 8, 10, 20, and 124 h, respectively). The efficiency of cleavage seems to be dependent upon the electronic environment about the ketal. ... [Pg.215]

The second type of trinuclear compounds containing (M302(02CR)(,(H20)3] and obtained by the reaction of M(CO)6 (M = Mo, W) with carboxylic acids, features a similar triangle of M-M bonded metal atoms but this time capped on both sides by hj-O atoms (Fig, 23.8d). Complexes m which either one or both of these capping atoms arc replaced by /iy-CR, alkylidene. [Pg.1026]

Safety. Since organic peroxides can be initiated by heat, mechanical shock, friction or contamination, an enormous problem in safety presents itself. Numerous examples of this problem have already been shown in this article. Additional examples include the foilowing methyl and ethyl hydroperoxides expld violently on heating or jarring, and their Ba salts also are extremely expl the alkylidene peroxides derived from low mw aldehydes and ketones are very sensitive and expld with considerable force polymeric peroxides of dimethyl ketene, -K>-0-C(CH3)2C(0)j-n, expld in the dry state by rubbing even at —80° peroxy acids, especially those of low mw, and diacetyl, dimethyl, dipropkmyl and methyl ethyl peroxides, when pure, must be handled only in small amts and... [Pg.680]

Amides can add to aldehydes in the presence of bases (so the nucleophile is actually RCONH ) or acids to give acylated amino alcohols, which often react further to give alkylidene or arylidene bisamides. If the R group contains an a hydrogen, water may split out. [Pg.1187]

Schemes 6-26 A proposed reaction pathway for Rh(l)-catalyzed cyclization of a,co-alkynoic acids to alkylidene lactones... Schemes 6-26 A proposed reaction pathway for Rh(l)-catalyzed cyclization of a,co-alkynoic acids to alkylidene lactones...
Langer and coworkers constructed diverse O- and N-heterocydic scaffolds, such as y-alkylidene-a-hydroxybutenolides and pyrrolo[3,2-b]pyrrol-2,5-diones, exploiting the well-established cyclization strategy of bisnucleophiles with oxalic acid derivatives [163], while Stockman s research group reported in this context on a novel oxime formation/Michael addition providing the structural core of the alkaloid perhydrohistrionicotoxin [164]. [Pg.94]

Ahn, Kim and coworkers, in the preparation of 4-alkylidene-3-arylmethylpyr-rolidines 6/1-77, used a Heck reaction of the vinyl bromide 6/1-76 in the presence of an arylboronic acid [47] (Scheme 6/1.19). ft has been assumed that the interme-... [Pg.371]


See other pages where Alkylidene acids is mentioned: [Pg.97]    [Pg.97]    [Pg.187]    [Pg.499]    [Pg.820]    [Pg.118]    [Pg.188]    [Pg.433]    [Pg.1059]    [Pg.1327]    [Pg.204]    [Pg.309]    [Pg.310]    [Pg.207]    [Pg.140]    [Pg.384]    [Pg.80]    [Pg.204]    [Pg.206]    [Pg.213]    [Pg.214]    [Pg.395]    [Pg.164]    [Pg.190]    [Pg.30]    [Pg.107]    [Pg.177]    [Pg.96]    [Pg.97]    [Pg.99]    [Pg.102]    [Pg.279]   
See also in sourсe #XX -- [ Pg.20 , Pg.106 ]




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Alkylidenation carboxylic acid derivatives

Keto acids via oxidation of alkylidene cycloalkanones

Ruthenium alkylidene catalyst acids

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