Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-<i>b</i>]pyridines at room temperature by a multi-component reaction

引用本文: Heshmatollah Alinezhad, Sahar Mohseni Tavakkoli, Pourya Biparva. Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction[J]. 催化学报, 2014, 35(4): 560-564. doi: 10.1016/S1872-2067(14)60034-6 shu

Citation: Heshmatollah Alinezhad, Sahar Mohseni Tavakkoli, Pourya Biparva. Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction[J]. Chinese Journal of Catalysis, 2014, 35(4): 560-564. doi: 10.1016/S1872-2067(14)60034-6 shu

Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

通讯作者: Heshmatollah Alinezhad

摘要: Cu doped ZnO nanocrystalline powder (10 mol%) has been found to be an efficient catalyst for the one-pot multi-component synthesis of fully substituted new indeno[1,2-b]pyridines through a combination of 1,3-indandione, propiophenone or acetophenone derivatives, aromatic aldehydes, and ammonium acetate in ethanol/H₂O at room temperature. The methodology is mild, efficient and high to excellent yielding.

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Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

1.
a Faculty of Chemistry, University of Mazandaran, Babolsar, 47415, Iran;

Corresponding author: Heshmatollah Alinezhad

Received Date: 02 November 2013
Available Online: 20 April 2014

Abstract: Cu doped ZnO nanocrystalline powder (10 mol%) has been found to be an efficient catalyst for the one-pot multi-component synthesis of fully substituted new indeno[1,2-b]pyridines through a combination of 1,3-indandione, propiophenone or acetophenone derivatives, aromatic aldehydes, and ammonium acetate in ethanol/H₂O at room temperature. The methodology is mild, efficient and high to excellent yielding.

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1. [1] Rad M N S, Behrouz S, Nekoei A R, Faghih Z, Khalafi-Nezhad A. Synthesis, 2011: 4068[1] Rad M N S, Behrouz S, Nekoei A R, Faghih Z, Khalafi-Nezhad A. Synthesis, 2011: 4068
2. [2] Ganem B. Acc Chem Res, 2009, 42: 463[2] Ganem B. Acc Chem Res, 2009, 42: 463
3. [3] Willis M C. Tetrahedron, 2009, 65: 8907[3] Willis M C. Tetrahedron, 2009, 65: 8907
4. [4] Kim B Y, Ahn J B, Lee H W, Kang S K, Lee J H, Shin J S, Ahn S K, Hong C I, Yoon S S. Eur J Med Chem, 2004, 39: 433[4] Kim B Y, Ahn J B, Lee H W, Kang S K, Lee J H, Shin J S, Ahn S K, Hong C I, Yoon S S. Eur J Med Chem, 2004, 39: 433
5. [5] Tapaswi P K, Mukhopadhyay C. ARKIVOC, 2011, (10): 276[5] Tapaswi P K, Mukhopadhyay C. ARKIVOC, 2011, (10): 276
6. [6] Matsumoto S, Miyamoto N, Hirayama T, Oki H, Okada K, Tawada M, Iwata H, Nakamura K, Yamasaki S, Miki H, Hori A, Imamura S. Bioorg Med Chem, 2013, 21: 7686[6] Matsumoto S, Miyamoto N, Hirayama T, Oki H, Okada K, Tawada M, Iwata H, Nakamura K, Yamasaki S, Miki H, Hori A, Imamura S. Bioorg Med Chem, 2013, 21: 7686
7. [7] Moustafa A H, El-Abbady S A, Gado S H, El-Borai M A. Pharmazie, 1983, 38: 221[7] Moustafa A H, El-Abbady S A, Gado S H, El-Borai M A. Pharmazie, 1983, 38: 221
8. [8] Prostakov N S, Soldatenkov A T, Radzhan P K, Fedorov V O, Fomichev A A, Rezakov V A. Chem Heterocycl Compd, 1982, 18: 390[8] Prostakov N S, Soldatenkov A T, Radzhan P K, Fedorov V O, Fomichev A A, Rezakov V A. Chem Heterocycl Compd, 1982, 18: 390
9. [9] Zhang J S, El-Shabrawy A R O, El-Shanawany M A, Schiff P L Jr, Slatkin D J. J Nat Prod, 1987, 50: 800[9] Zhang J S, El-Shabrawy A R O, El-Shanawany M A, Schiff P L Jr, Slatkin D J. J Nat Prod, 1987, 50: 800
10. [10] Tadic D, Cassels B K, Cave A, Goulart M O F, de Oliveira A B. Phytochemistry, 1987, 26: 1551[10] Tadic D, Cassels B K, Cave A, Goulart M O F, de Oliveira A B. Phytochemistry, 1987, 26: 1551
11. [11] Prostakov N S, Vasilev G A, Zvolinskii V P, Varlamov A V, Savina A A, Sorokin O I, Lopatina N D. Chem Heterocycl Compd, 1975, 11: 97[11] Prostakov N S, Vasilev G A, Zvolinskii V P, Varlamov A V, Savina A A, Sorokin O I, Lopatina N D. Chem Heterocycl Compd, 1975, 11: 97
12. [12] Padwa A, Heidelbaugh T M, Kuethe J T. J Org Chem, 2000, 65: 2368[12] Padwa A, Heidelbaugh T M, Kuethe J T. J Org Chem, 2000, 65: 2368
13. [13] Alves T, de Oliveira A B, Snieckus V. Tetrahedron Lett, 1988, 29: 2135[13] Alves T, de Oliveira A B, Snieckus V. Tetrahedron Lett, 1988, 29: 2135
14. [14] Tu S J, Jiang B, Jia R H, Zhang J Y, Zhang Y. Tetrahedron Lett, 2007, 48: 1369[14] Tu S J, Jiang B, Jia R H, Zhang J Y, Zhang Y. Tetrahedron Lett, 2007, 48: 1369
15. [15] Tu S J, Jiang B, Yao C S, Jiang H, Zhang J Y, Jia R H, Zhang Y. Synthesis, 2007: 1366[15] Tu S J, Jiang B, Yao C S, Jiang H, Zhang J Y, Jia R H, Zhang Y. Synthesis, 2007: 1366
16. [16] Golego N, Studenikin S A, Cocivera M. J Electrochem Soc, 2000, 147: 1592[16] Golego N, Studenikin S A, Cocivera M. J Electrochem Soc, 2000, 147: 1592
17. [17] Lin Y H, Zhang Z T, Tang Z L, Yuan F L, Li J L. Adv Mater Opt Electron, 1999, 9: 205[17] Lin Y H, Zhang Z T, Tang Z L, Yuan F L, Li J L. Adv Mater Opt Electron, 1999, 9: 205
18. [18] Wang X D, Song J H, Liu J, Wang Z L. Science, 2007, 316: 102[18] Wang X D, Song J H, Liu J, Wang Z L. Science, 2007, 316: 102
19. [19] Keren K, Berman R S, Buchstab E, Sivan U, Braun E. Science, 2003, 302: 1380[19] Keren K, Berman R S, Buchstab E, Sivan U, Braun E. Science, 2003, 302: 1380
20. [20] Wang Z L. Mater Sci Eng R, 2009, 64: 33[20] Wang Z L. Mater Sci Eng R, 2009, 64: 33
21. [21] Zhang L L, Ding Y L, Povey M, York D. Progr Nat Sci, 2008, 18: 939[21] Zhang L L, Ding Y L, Povey M, York D. Progr Nat Sci, 2008, 18: 939
22. [22] Tao Y M, Ma S Y, Chen H X, Meng J X, Hou L L, Jia Y F, Shang X R. Vacuum, 2011, 85: 744[22] Tao Y M, Ma S Y, Chen H X, Meng J X, Hou L L, Jia Y F, Shang X R. Vacuum, 2011, 85: 744
23. [23] Zhang Z, Yi J B, Ding J, Wong L M, Seng H L, Wang S J, Tao J G, Li G P, Xing G Z, Sum T C, Huan C H A, Wu T. J Phys Chem C, 2008, 112: 9579[23] Zhang Z, Yi J B, Ding J, Wong L M, Seng H L, Wang S J, Tao J G, Li G P, Xing G Z, Sum T C, Huan C H A, Wu T. J Phys Chem C, 2008, 112: 9579
24. [24] Alinezhad H, Mohseni Tavakkoli S. The Sci World J, 2013, 2013: 1[24] Alinezhad H, Mohseni Tavakkoli S. The Sci World J, 2013, 2013: 1

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通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

通讯作者: Heshmatollah Alinezhad

English

Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

Corresponding author: Heshmatollah Alinezhad

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通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

通讯作者: Heshmatollah Alinezhad

English

Cu-doped ZnO nanocrystalline powder catalyzed one-pot synthesis of fully substituted new indeno[1,2-b]pyridines at room temperature by a multi-component reaction

Corresponding author: Heshmatollah Alinezhad

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

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CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

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CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

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