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在高硅/铝比的酸性沸石分子筛HY上实现了Knoevenagel缩合反应. Brnsted酸和Lewis酸均可催化Knoevenagel缩合反应. 考察了羰基化合物和活泼亚甲基化合物的反应活性顺序. 结果表明,羰基化合物的羰基极化程度越高,反应越容易进行; 不同于碱催化时的Knoevenagel缩合反应,活泼亚甲基化合物的活泼氢的酸性并不是影响其反应活性的重要因素.

参考文献

[1] Pandya K C;Surange V R .[J].Journal of the Indian Chemical Society,1934,11:824.
[2] Clinton R O;Laskowski S C .[J].Journal of the American Chemical Society,1949,71(11):3602.
[3] Alexander E R;Cope A C .[J].Journal of the American Chemical Society,1944,66(06):886.
[4] Fieser L F;Adams R;Buchmann W E.Organic Reactions (Vol 15)[M].New York:John Wiley and Sons,Inc,1966:206.
[5] 左伯军 .[D].济南:山东大学,1997.
[6] Jaenicke S;Chuah G K;Lin X H;Hu X C .[J].Microporous and Mesoporous Materials,2000,35/36:143.
[7] Sebti S. .Fluorapatite: new solid catalyst of the knoevenagel reaction in heterogeneous media without solvent[J].Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications,2000(2):187-190.
[8] Cope A C;Hoyle K E .[J].Journal of the American Chemical Society,1941,63(03):733.
[9] Lange J;Kanabus-Kaminska J M;Kral A .[J].Synthetic Communications,1980,10(06):473.
[10] Corma A;Martin-Aranda R M;Sanchez F .[J].Journal of Catalysis,1990,126(01):192.
[11] Elimil E L .[J].Organic Syntheses,1970,50:28.
[12] Chang C D;Lang W H;Bell W K.Catalysis of Organic Reactions[A].New York:Dekker,1981:73.
[13] Corson B B;Smith M B .[J].Organic Syntheses,1964,1:179.
[14] B.J.ZUO,Y.D.MA,Y.TIAN.Synthesis of Dibenzo-sulfur-heterocycles through reaction of Diphenyl-type compounds with elemental sulfur over USY zeolite[J].Chinese Chemical Letters,1997(10):849.
[15] W.JIANG,Q.L.WANG,Y.D.MA.Zeolite-catalyzed thionation of diphenyl-type compounds[J].Chinese Chemical Letters,1997(05):381.
[16] WANG Q L;Ma Y D;Jiang W .[J].Applied Catalysis A:General,1997,165:199.
[17] Foucaud P R.[J].Bulletin de la Societe Chimique de France,1964:1873.
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