Разработка каталитических систем для осуществления альдольной конденсации низших альдегидов (1091786), страница 20
Текст из файла (страница 20)
Chem., 2009, Vol. 15, № 13, P. 3093-102128. Córdova A. Direct catalytic asymmetric cross-aldol reactions in ionic liquidmedia // Tetrahedron Lett., 2004, Vol. 45, P. 3949-3952129. Tang Z., Jiang F., Yu L-T., Cui X., Gong L-Z., Mi A-Q., Jiang Y-Z., Wu YD. Novel small organic molecules for a highly enantioselective direct aldol reaction // J.Am. Chem. Soc., 2003, Vol. 125, P. 5262-5263130.NorthrupA.B.,MangionI.K.,HettcheF.,MacMillanD.W.C.Enantioselective organocatalytic direct aldol reaction of a-oxyladehydes: Step one in a145two-step synthesis of carbohydrates // Angew. Chem. Int.
Ed., 2004, Vol. 43, P. 21522154131.KunzR.K.,MacMillanD.W.C.Enantioselectiveorganocatalyticcyclopropanations. The identification of a new class of iminium catalyst based upondirected electrostatic activations // J. Am. Chem. Soc., 2005, Vol. 127, P. 3240-3241132. Hernández J.G., Juaristi E. Efficient ball-mill procedure in the ‘green’asymmetric aldol reaction organocatalyzed by (S)-proline-containing dipeptides in thepresence of water // Tetrahedron Lett., 2011, Vol. 67, № 36, P.
6953-6959133. Casas J., Engqvist M., Ibrahem I., Kaynak B., Córdova A. Direct amino acidcatalyzed asymmetric synthesis of polyketide sugars // Angew. Chem. Int. Ed., 2005,Vol. 44, P. 1343-1345134. Knoevenagel E. 1,5-Diketone. (Erste Mittheilung) // Liebigs Annalen derChemie, 1894, Bd. 281, S. 25-27135. Enders D., Nguyen T.V. Secondary amine catalyzed retro-aldol reactions ofenals and enones: one-pot conversion of enals to α-substituted derivatives //Tetrahedron Lett., 2012, Vol.
53, № 16, P. 2091-2095136. Shrikhande J.J., Gawande M.B., Jayaram R.V. Cross-aldol and Knoevenagelcondensation reactions in aqueous micellar media // Catalysis Comm., 2008, Vol. 9, №6, P. 1010-1016137. Reymond J.L., Chen Y.W. Catalytic enantioselective aldol reaction with anartificial aldolase assembled from a primary amine and an antibody // J. Org. Chem.,1995, Vol. 60, № 21, P.
6970-6979138. Denmark S.E., Stavenger R.A. The chemistry of trichlorosilyl enolates. 2.Highly-selective asymmetric aldol additions of ketone enolates // Accounts of ChemicalRes., 2000, Vol. 33, P. 432-440139. Пат. 2518416 США, Preparation of acroleins / N.M. Bortnick140. Пат. 2639295 США, Manufacture of unsaturated aldehydes / J. Hagemeyer,J. Hugh.141.ErkkiläA.,PihkoP.M.Rapidorganocatalytic aldehyde-aldehydecondensation reactions // European J. Org.
Chem., 2007, P. 153-165146142. Bulcsú R, Anikó C., Árpád M. Mechanokémiai szintézissel készült SiO2hordozós heterofoszforvolfrámsav katalizátorok vizsgálata // Vegyészkonferencia,Hajdúszoboszló, Program és el ő adásösszefoglalók, 2003, P-91, P. 139143. Rác B., Molnár Á., Forgó P., Mohai M., Bertóti I. A comparative study ofsolid sulfonic acid catalysts based on various ordered mesoporous silica materials // J.Mol. Catalysis A., 2006, Vol.
244, P. 46144. Shimizu K., Hayashi E., Inokuchi T., Kodama T., Hagiwara H., Kitayama Y.Self-aldol condensation of unmodified aldehydes catalysed by secondary-amineimmobilised in FSM-16 silica // Tetrahedron Lett., 2002, Vol. 43, P. 9073-9075145. Sharma S.K., Shukla R.S., Parikh P.A., Jasra R.V. The multi-step reactionsfor the synthesis of C8 aldehydes and alcohol from propene in a single pot using an ecofriendly multi-functional catalyst system: Kinetic performance for parametricoptimization // J. Mol. Catalysis A., 2009, Vol. 304, № 1, P.
33-39146. Patel H.A., Sharma S.K., Jasra R.V. Synthetic talc as a solid base catalyst forcondensation of aldehydes and ketones // J. Mol. Catalysis A., 2008, Vol. 286, P. 31-40147. Пат. 6307093 США, Organic compounds and processes for their manufacture/ G.A. David.148. Пат. 2727330 ФРГ, Verfahren Zur Herstellung Von 2-methyl-penten-2-al-1 /W. Schoenleben, H. Hoffmann, W. Lengsfeld, H. Mueller149.
Telalović S., Karmee S.K., Ramanathan A., Hanefeld U. Al-TUD-1:Introducing tetrahedral aluminium // J. Mol. Catalysis A., 2013, Vol. 368-369, P. 88-94150. Zeidan R.K., Davis M.E. The effect of acid-base pairing on catalysis: Anefficient acid–base functionalized catalyst for aldol condensation // J. Catalysis, 2007,Vol. 247, № 2, P. 379-382147151. Dumitriu E., Hulea V., Chelaru C., Catrinescu C., Tichit D., Durand R.Influence of the acid-base properties of solid catalysts derived from hydrotalcite-likecompounds on the condensation of formaldehyde and acetaldehyde // Appl. CatalysisA., 1999, Vol. 178, P. 145-157152. Dumitriu E., Bilba N., Lupascu M., Azzouz A., Hulea V., Cirje G., Nibou D.Vapor-phase condensation of formaldehyde and acetaldehyde into acrolein over zeolites// J.
Catalysis, 1994, Vol. 147, № 1, P. 133-139153. Dumitriu E., Hulea V., Bilba N., Carja G., Azzouz A. Synthesis of acrolein byvapor phase condensation of formaldehyde and acetaldehyde over oxides loadedzeolites // J. Mol. Catalysis, 1993, Vol. 79, № 1, P. 175-185154.
Madhavi G., Kulkarni S.J., Murthy K.R., Viswanathan V., Raghavan K.V.Side chain alkylation of 2-picoline with formaldehyde over alkali modified zeolites // J.Porous Materials, 2007, Vol. 14, P. 433-441155. Ai M. Reaction of methyl acetate with methylal in the presence of oxygen //Studies in Surface Science and Catalysis, 1992, Vol. 72, P. 101-108156. Ai M. Formation of glyoxal by oxidative dehydrogenation of ethylene glycol// Bull. Chem.
Soc. Japan, 2002, Vol. 75, P. 375-381157. Davies S.G., Fletcher A.M., Hughes D.G., Lee J.A., Price P.D., Roberts P.M.,Russell A.J., Smith A.D., Thomson J.E., Williams O.M. Asymmetric synthesis ofpiperidines and octahydroindolizines using a one-pot ring-closure/N-debenzylationprocedure // Tetrahedron Lett., 2011, Vol. 67, № 51, P.
9975-9992158. Ueda W., Ohwa H., Iwasaki K., Kuwabara T., Ohshida T., Morikawa Y.Methanol-based synthetic reactions over solid-base catalyst // Acid-Base Catalysis II,Kodansha Ltd., 1994, P. 35-46159. Cojocariu A.M., Mutin P.H., Dumitriu E., Aboulaich A., Vioux A., Fajula F.,Hulea V. Non-hydrolytic SiO2-TiO2 mesoporous xerogels-efficient catalysts for themild oxidation of sulfur organic compounds with hydrogen peroxide // Catalysis Today,2010, Vol.
157, P. 270-274160. Azzouz A., Messad-Challal D., Dumitriu E., Amokrane S., Nibou D., AbbadB., Chertouk-Moknine L., Saber M., Carja G. Vapor phase alkylation of ammonia with148octanol over pillard and wanyl ion-exchanged montmorillonites // Rev. Roumaine deChimie, 1997, Vol. 42, № 10, P.
1019-1024161. Khémaissia S., Nibou D., Amokrane S., Lebaili N. Elaboration andcharacterization of high silica ZSM-5 and mordenite solid microporous materials // J.Appl. Sci., 2007, Vol. 7, P. 720-723162. Noda Pérez C., Pérez C.A., Henriques C.A., Monteiro J.L.F. Hydrotalcites asprecursors for Mg,Al-mixed oxides used as catalysts on the aldol condensation of citralwith acetone // Appl.
Catalysis A., 2004, Vol. 272, P. 229-240163. Antunes W.M., de Oliveira Veloso C., Henriques С.А. Transesterification ofsoybean oil with methanolcatalyzed by basic solids // Catalysis Today, 2008, Vol. 133135, P. 548-554164. Grygar T., Hradil D., Bezdička P., Doušová B., Čapek L., Schneeweiss O.Fe(III)-modified montmorillonite and bentonite: synthesis, chemical and UV-visspectral characterization, arsenic sorption, and catalysis of oxidative dehydrogenation ofpropane // Clays and Clay Minerals, 2007, Vol. 55, P. 165-176165. Azzouz A., Messad D., Nistor D., Catrinescu C., Zvolinschi A., Asaftei S.Vapor phase aldol condensation over fully ion-exchanged montmorillonite-richcatalysts // Appl.
Catalysis A., 2003, Vol. 241, P. 1-13166. Fyfe C.A., Thomas J.M., Klinowski J., Gobbi G.C. Magic-angle-spinningNMR (MAS-NMR) spectroscopy and the structure of zeolites // Angew. Chem. Int. Ed.,1983, Vol. 22, P. 259-275167. Xu W., Liu X., Ren J., Zhang P., Wang Y., Guo Y., Guo Y., Lu G. A novelmesoporous Pd/cobalt aluminate bifunctional catalyst for aldol condensation andfollowing hydrogenation // Catalysis Comm., 2010, Vol. 11, P.
721-726168. Пат. 3702886 США, Crystalline zeolite ZSM-S and method / R.J. Argauer,G.R. Landolt169. Venuto B.P., Habib E.T. Fluid catalytic cracking with zeolite catalysts /Chemical Industries. Vol. 1, N.Y.: Marcel Dekker Inc., 1979, Р. 303170. Kokotailo G.T., Lawton S.L., Olson D.H., Meier W.M. Structure of syntheticzeolite ZSM-5 // Nature, 1978, Vol.
272, P. 437-438149171. Weisz P.B. Molecular shape selective catalysis // Pure Appl. Chem., 1980,Vol. 52, P. 2091-2103172. Hölderich W. New horizons in catalysis using modified and unmodifiedpentasil zeolites // J. Zeolites Microporous Crystals, 1986, Vol. 28, P. 827-834173. Niwa M., Senoh N., Hibino T., Nakatsuka Y., Murakami Y. Reactant shapeselectivity for cracking of linear paraffin on HZSM-5 modified by CVD of siliconalkoxide: A strong dependence upon the reaction temperature // Zeolites MicroporousCrystals, 1994, Vol. 83, 155-162174.
Hölderich W., Hesse M., Näumann F. Zeolithe: Katalysatoren für dieSynthese organischer Verbindungen // Angew. Chem. Int. Ed., 1988, Vol. 100, P. 232251175. Hölderich W. New aspects in the performance of heterogeneous catalysts forintermediates and fine chemicals // Heterogeneous Catalysis and Fine Chemicals, Proc.In. Symp., 15-17 March 1988, Vol. 41, P. 1-417176. Евр. Пат.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
