Разработка каталитических систем для осуществления альдольной конденсации низших альдегидов (1091786), страница 21
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№ 0013600, Production of alkenols and alkanediols bycondensation of aldehyde and ethylenically unsaturated compounds / C.C. Dayton, L.W.Harry, M.N. James177. Chang C.D., Lang W.H., Bell W.K. Catalysis of Organic Reaction / Ed.: W.R.Moser, N.Y.: Marcel Dekker Inc., 1981. Р. 647178. Hölderich W. New horizons in catalysis using modified and unmodifiedpentasil zeolites // Pure Appl. Chem., 1986, Vol. 58, № 10, P. 1383-1388179.
Vervecken M., Servotte Y., Wydoodt M., Jacobs L., Martens J.A, Jacobs P.A.Zeolite-induced selectivity in the conversion of the lower aliphatic carboxylic acids // J.Chemical Reactions in Organic and Inorganic Constrained Systems, 1986, Vol. 165, P.95-114180. Пат. 4433174 США, Process for preparation of alpha, beta-unsaturatedaldehydes using AMS-1B borosilicate crystalline molecular sieve / G.P.
Hagen181. Cobzaru C., Oprea S., Dumitriu E., Hulea V., Gas phase aldol condensation oflower aldehydes over clinoptilolite rich natural zeolites // Appl. Catalysis A., 2008, Vol.351, № 2, P. 253-258150182. Ungureanu A., Royer S., Hoang T.V., Trong On D., Dumitriu E., KaliaguineS. Aldol condensation of aldehydes over semicrystalline zeolitic-mesoporous UL-ZSM5 // Microporous and Mesoporous Materials, 2005, Vol. 84, P. 283-296183. Dumitriu E., Meloni D., Monaci R., Solinas V.
Liquid-phase alkylation ofphenol with t-butanol over various catalysts derived from MWW-type precursors //Comptes rendus – Chimie, 2005, Vol. 8, P. 441-456184. Zucca P.,Vinci C.,Rescigno A., Dumitriu E., Sanjust E. Is the bleaching ofphenosafranine by hydrogen peroxide oxidation catalyzed by silica-supported5,10,15,20-tetrakis-(sulfonatophenyl)porphine-Mn(III) really biomimetic // J.
Mol.Catalysis. A., 2010, Vol. 321, P. 27-33184. Hulea V., Maciuca A-L., Cojocariu A-M., Ciocan C-E., Dumitriu E. Newheterogeneous catalysts for mild oxidation of S-containing organic compounds //Comptes rendus – Chimie, 2009, Vol. 12, P. 723-730185. Cojocariu A.M., Mutin P.H., Dumitriu E., Fajula F., Vioux A., Hulea V.
Mildoxidation of bulky organic compounds with hydrogen peroxide over mesoporous TiO 2SiO2 xerogels prepared by non-hydrolytic sol-gel // Appl. Catalysis B. Environmental,2010, Vol. 97, P. 407-413186. Andreu C., del Olmo M., Asensio G. Effect of addition of Lewis/Brönstedacids in the asymmetric aldol condensation catalyzed by trifluoroacetate salts of prolinebased dipeptides // Tetrahedron Lett., 2012, Vol. 68, № 38, P. 7966-7972187. Babler J.H., Atwood M.C., Freaney J.E., Viszlay A.R. The role of imine–enamine tautomerism in effecting cross-aldol condensations // Tetrahedron Lett., 2007,Vol. 48, № 43, P. 7665-7667188. Xu Q., Yu J., Han F., Hu J., Chen W., Yang L. Achiral additives dramaticallyenhanceenantioselectivitiesinthe BINOL–Ti(IV)complexcatalyzedaldolcondensations of aldehydes with Chan’s diene // Tetrahedron: Asymm., 2010, Vol. 21,№ 2, P. 156-158189.
Frey A.M., Karmee S.K., de Jong K.P., Bitter J.H., Hanefeld U. SupportedLa2O3 and MgO Nanoparticles as Solid Base Catalysts for Aldol Reactions While151Suppressing Dehydration at Room Temperature // J. Chem. Cat. Chem., 2013, P. 594600190. Sakthivel K., Notz W., Bui T., Barbas C.F., Amino acid catalyzed directasymmetric aldol reactions: A bioorganic approach to catalytic asymmetric carboncarbon bond-forming reactions // J.
Am. Chem. Soc., 2001, Vol. 123, P. 5260-5267191. Yamaguchi A., Matsunaga S., Shibasaki M. Direct catalytic asymmetricmannich-type reactions of g-butenolides:Effectiveness of bronsted acid in chiral metalcatalysis // Org. Lett., 2008, Vol. 10, P. 2319-2322192. Takita R., Harada S., Ohshima T., Matsunaga S., Shibasaki M.
Catalyticenantioselective addition of terminal alkynes to aldehydes:preparation of (S)-(-)-1,3diphenyl-2-propyn-1-ol and(S)-(-)-4-methyl-1-phenyl-2-pentyn-1,4-diol // Org. Synth.,2008, Vol. 85, P. 118-120193. Nitabaru T., Kumagai N., Shibasaki M. A catalytic asymmetric anti-selectivenitroaldol reaction with a neodymium-sodium heterobimetallic complex // TetrahedronLett., 2008, Vol. 49, P. 272-274194. Iding H., Dünnwald T., Greiner L., Liese A., Müller M., Siegert P.,Grotzinger J., Demir A.S., Pohl M.
Benzoylformate decarboxylase from Pseudomonasputida as stable catalyst for the synthesis of chiral 2-hydroxy ketones // Europ. J.Chem., 2000, Vol. 6, P. 1483-1495195. Domınguez de Marıа P., Stillger T., Pohl M., Wallert S., Drauz K., Gröger H.,Trauthwein H., Liese A. Preparative enantioselective synthesis of benzoins and (R)-2hydroxy-1-phenylpropanone using benzaldehyde lyase // J. Mol. Catalysis B., 2006,Vol. 38, P. 43-47196. Пат.
2197258 США, Preparation of acrolein / D.M. Alexander197. Пат. 2270705 США, Production of acrolein / K.M. Herstein198. Пат. 2334091 США, Production of acrolein / K.M. Herstein199. Пат. 2486842 США, Catalytic oxidation of hydrocarbons / G.W. Hearne,M.L.
Adams200. Пат. 2451485 США, Production of unsaturated carbonylic compounds / G.W.Hearne, M.L. Adams152201. Пат. 2383711 США, Preparation of alkenals and alkenones / A. Clark, R.S.Shutt202. Пат. 2608585 США, Reactivation of cuprous oxide oxidation catalysts / K.D.Detling, S. Thurston203. Пат. 694354 Великобритания, Oxidation of olefines / D.J. Hadley204. Андреас Ф., Гребе К. Химия и технология пропилена. Л.: Химия, 1973,C.
368205. А.с. 159515 СССР, 19631228 A1 800696/23-4. 27.10.1962, Способполучения альфа, бета-ненасыщенных альдегидов и кетонов / В.Р. Паннус,Л.М. Тищенко, Е.С. Шестухин206. Пат. 625330 Великобритания, Improvements in and process for themanufacture of acrolein / E.P. Goodings, D.J. Hadley207. Пат. 658240 Великобритания, Catalysts / D.J. Hadley, E.P. Goodings208. Пат. 877450 Франция, Réchaud électrique / J. Fernand209 Пат. 727318 Великобритания, Manufacture of an unsaturated aldehyde /D.J. Hadley210. Пат. 875160 Великобритания, Improvements relating to the production ofunsaturated aldehydes / Е.J.
Gasson211. Пат. 1325538 Франция, Procédé de fabrication d'aldéhydes non saturés/ Asahi Chemical Ind.212. Пат. 658179 Великобритания, Oxidation of olefines / D.J. Hadley,E.P. Goodings213. Пат. 678557 Великобритания, Manufacture of aldehydes / D.J. Hadley, R.Heap214. Пат. 806440 Франция, Dispositif pour le transport d'objets de grandesdimensions / E. Boilot215. Пат. 694354 Великобритания, Oxidation of olefines / D.J.
Hadley216. Пат. 2245582 США, Process for the manufacture of unsaturated aldehydes /M. Gallagher, L.H. Rudolph153217. Пат. 2246037 США, Process for the manufacture of unsaturated aldehydes /M. Gallagher, L. H. Rudolph218. Пат. 101032 Швеция, Sätt att framställa kondensationsprodukter avformaldehyd / H.
Schulz, H. Walter219. Пат. 101145 Швеция, Sätt att framställa kondensationsprodukter avformaldehyd / H. Schulz, H. Walter220. Пат. 2288306 США, Production of condensation products / H. Wagner221. Kamio M, Uchiyama T, Arima N, Itoh K, Ishikawa T, Hori T, Uchino H.Role of alpha chain-IL-2 complex in the formation of the ternary complex of IL-2 andhigh-affinity IL-2 receptor // J. Int. Immunology, 1990, Vol.
2, № 6, P. 521-530222. Пат. 2294955 США, Process for the manufacture of unsaturated aldehydes /J.H. Brant223. Arima N., Kamio M., Okuma M., Ju G., Uchiyama T. The IL-2 receptoralpha-chain alters the binding of IL-2 to the beta-chain // J. Int. Immunology, 1991,P. 3396-3401224.
Saito Y., Ogura T., Kamio M., Sabe H., Uchiyama T., Honjo T. Stepwiseformation of the high-affinity complex of the interleukin 2 receptor // J. Int.Immunology, 1990, Vol. 2, P. 1667-1677225. Пат. 1203243 ФРГ, Verfahren zur Herstellung von alpha, beta-ungesaettigtenAldehyden und Ketonen / R.N. Watts, W.J. Porter, J.A. Wingate, J.A. Hanan226. Vít Z., Nondek L., Málek J. Liquid-phase aldol condensation ofcyclohexanone on aluminium and iron oxides // Coll.
of Czechoslovak Chem. Comm.,1982, Vol. 47, P. 2235-2245227. Toma Š, Gáplovský A. Kinetic study of cyclization of 1-acyl-1'alkenoylferrocenes. The effect of substitution on the donor and acceptor of Michaeladdition upon activation parameters of the reaction // Coll. of Czechoslovak Chem.Comm., 1982, Vol. 47, P. 2246-2257228.
Nondek Z., Málek J. Aldol condensation of butyraldehyde in the liquid phasecatalysed by aluminium, iron and chromium sesquioxides // Coll. of CzechoslovakChem. Comm., 1979, Vol. 44, № 8, P. 2384-2392154229. Záletová J., Dzurilla M., Kutschy P., Pazdera P., Kováčik V., Aldölfi J.,Bekešov S. Synthesis of 4,6-disubstituted-2-(1H-indol-3-yl)benzothiazoles // Coll. ofCzechoslovak Chem.
Comm., 2004, Vol. 69, № 2, P. 453-460230. Vashishtha M., Mishra M., O. Shah D., A novel approach for selective crossaldol condensation using reusable NaOH-cationic micellar systems // Appl. Catalysis A.,2013, 466, P. 38-44231. Гордон А., Форд Р. Спутник химика. Физико-химические свойства,методики, библиография. М.: Мир, 1976, C. 541232. Tietze L.F., Eicher T. Reaktionen und Synthesen im organisch-chemischenPraktikum und Forschungslaboratorium.
Stuttgart: Georg Thieme Verlag, 1991, Р. 259233. Сайт NIST www.nist.gov Agilent NIST 98.
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