Aldol Condensations of Aldehydes over Disodium Phthalocyanine
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چکیده
منابع مشابه
Aldol Condensation of Aldehydes and Ketones over Solid Base Catalysts
Introduction Industrially condensation reactions are of great importance in the production of a number of key compounds. These include 2-ethyl hexanol, methyl isobutyl ketone (MIBK) and Guerbet alcohols. Over 1.5 million tonnes of these chemicals are produced worldwide every year using homogeneous bases such as NaOH and Ca(OH)2. It has been estimated for these compounds that 30% of the selling ...
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The first enantioselective catalytic direct cross-aldol reaction that employs nonequivalent aldehydes has been accomplished using proline as the reaction catalyst. Structural variation in both the aldol donor (R1 = Me, n-Bu, Bn, 91 to >99%) and aldol acceptor (R2 = I-Pr, I-Bu, c-C6H11, Et, Ph, 97-99% ee) are possible while maintaining high reaction efficiency (75-88% yield). Significantly, this...
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Rehydration of Mg-Al hydrotalcite in the liquid phase using ultrasounds or a high stirring speed leads to nanoplatelets with surface areas of 400 m(2) g(-1), displaying catalytic activities in aldol condensations up to 8 times higher than the best catalytic system reported in the literature.
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An environmentally benign, clean and general protocol was developed for the synthesis of aryl and heteroaryl trans-chalcones. This method involved solvent-free reaction conditions under microwave irradiation in the presence of a clay-based catalyst, and afforded the target compounds in good yields and short reaction times. Furthermore, the same conditions allowed the synthesis of symmetrical, d...
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The enzyme 4-oxalocrotonate tautomerase (4-OT) from Pseudomonas putida mt-2 takes part in a catabolic pathway for aromatic hydrocarbons, where it catalyzes the conversion of 2hydroxyhexa-2,4-dienedioate into 2-oxohexa-3-enedioate. This tautomerase can also promiscuously catalyze carbon-carbon bond-forming reactions, including various types of aldol reactions, by using its amino-terminal proline...
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1973
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.46.518