Superparamagnetic CuFeO2 Nanoparticles in Deep Eutectic Solvent: an Efficient and Recyclable Catalytic System for the Synthesis of Imidazo[1,2-a]pyridines
Superparamagnetic CuFeO2 nanoparticles were prepared and characterized by XRD, SEM, TEM, FRIR spectroscopy, and vibrating sample magnetometry techniques. The catalytic activity of CuFeO2 nanoparticles was investigated in the one‐pot, three‐component reaction of 2‐aminopyridines, aldehydes, and alkyn...
Saved in:
| Published in | ChemCatChem Vol. 6; no. 10; pp. 2854 - 2859 |
|---|---|
| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
01.10.2014
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Superparamagnetic CuFeO2 nanoparticles were prepared and characterized by XRD, SEM, TEM, FRIR spectroscopy, and vibrating sample magnetometry techniques. The catalytic activity of CuFeO2 nanoparticles was investigated in the one‐pot, three‐component reaction of 2‐aminopyridines, aldehydes, and alkynes using citric acid–dimethylurea melt as a green solvent. An array of imidazo[1,2‐a]pyridines were obtained in good to excellent yields. The catalytic system can be successfully reused six times with keeping its catalytic performance.
Green solvent and efficient catalyst: A recyclable catalytic system comprising magnetically recoverable CuFeO2 nanoparticles in a citric acid–dimethylurea melt is established as an efficient and environmentally friendly system for the one‐pot synthesis of imidazo[1,2‐a]pyridines. |
|---|---|
| AbstractList | Superparamagnetic CuFeO2 nanoparticles were prepared and characterized by XRD, SEM, TEM, FRIR spectroscopy, and vibrating sample magnetometry techniques. The catalytic activity of CuFeO2 nanoparticles was investigated in the one-pot, three-component reaction of 2-aminopyridines, aldehydes, and alkynes using citric acid-dimethylurea melt as a green solvent. An array of imidazo[1,2-a]pyridines were obtained in good to excellent yields. The catalytic system can be successfully reused six times with keeping its catalytic performance. [PUBLICATION ABSTRACT] Superparamagnetic CuFeO2 nanoparticles were prepared and characterized by XRD, SEM, TEM, FRIR spectroscopy, and vibrating sample magnetometry techniques. The catalytic activity of CuFeO2 nanoparticles was investigated in the one‐pot, three‐component reaction of 2‐aminopyridines, aldehydes, and alkynes using citric acid–dimethylurea melt as a green solvent. An array of imidazo[1,2‐a]pyridines were obtained in good to excellent yields. The catalytic system can be successfully reused six times with keeping its catalytic performance. Green solvent and efficient catalyst: A recyclable catalytic system comprising magnetically recoverable CuFeO2 nanoparticles in a citric acid–dimethylurea melt is established as an efficient and environmentally friendly system for the one‐pot synthesis of imidazo[1,2‐a]pyridines. |
| Author | Ma, Er-Qian Lu, Jun Li, Xiao-Tang Mo, Li-Ping Zhang, Zhan-Hui |
| Author_xml | – sequence: 1 givenname: Jun surname: Lu fullname: Lu, Jun organization: College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024 (P.R. China), Fax: (+86) 311-80787431 – sequence: 2 givenname: Xiao-Tang surname: Li fullname: Li, Xiao-Tang organization: College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024 (P.R. China), Fax: (+86) 311-80787431 – sequence: 3 givenname: Er-Qian surname: Ma fullname: Ma, Er-Qian organization: College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024 (P.R. China), Fax: (+86) 311-80787431 – sequence: 4 givenname: Li-Ping surname: Mo fullname: Mo, Li-Ping organization: College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024 (P.R. China), Fax: (+86) 311-80787431 – sequence: 5 givenname: Zhan-Hui surname: Zhang fullname: Zhang, Zhan-Hui email: zhanhui@mail.nankai.edu.cn organization: College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024 (P.R. China), Fax: (+86) 311-80787431 |
| BookMark | eNo9kctO5DAQRa0RSMNry9oSW9Jjx3l5dih0MyAEAlqANBpZjl1hDGkn2AkQPoWvxU2jXpVv-d4q6dQ22rCtBYT2KZlQQuJfSvVqEhOakDih6Q-0RYssj1jB-cb6XZCfaNv7R0IyzvJ0C33cDB24Tjq5kA8WeqNwOczgMsYX0rahHzoNeGwsPgbo8HToQS1dN23zArb_jaXF07o2ygQVhMbXoEbVyKoBXMpeNuOXffQ9LHDdOtz_hyBtKN543Nb4dGG0fG__0sM4kv-60RltLPhdtFnLxsPed91B89l0Xv6Jzi9PTsuj88iwnKQR1xWA4kmdVipnKeVVkdUsKTKS6YzGOlbLf5pxxSsIbIo6qQKhXOdaq0KyHXSwGtu59nkA34vHdnA2bBQ0LcKEhLM0uPjK9WoaGEXnzEK6UVAiluzFkr1YsxdlOS_XKmSjVdYEBm_rrHRPIsvDFcTdxYmg9zOSnN0yccU-ARzJjdY |
| ContentType | Journal Article |
| Copyright | 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| Copyright_xml | – notice: 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| DBID | BSCLL |
| DOI | 10.1002/cctc.201402415 |
| DatabaseName | Istex |
| DatabaseTitleList | |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1867-3899 |
| EndPage | 2859 |
| ExternalDocumentID | 3452516971 CCTC201402415 ark_67375_WNG_1XF04JV3_Q |
| Genre | article |
| GrantInformation_xml | – fundername: National Natural Science Foundation of China (NNSFC) funderid: 21272053; 21072042 |
| GroupedDBID | 05W 0R~ 1OC 31~ 33P 4.4 5DZ 77Q 8-1 A00 AAESR AAHHS AAIHA AANLZ AASGY AAXRX AAYOK AAZKR ABCUV ABDBF ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACIWK ACPOU ACXBN ACXQS ADBBV ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AENEX AEQDE AEUYR AFBPY AFFPM AFGKR AFZJQ AHBTC AITYG AIURR AIWBW AJBDE ALMA_UNASSIGNED_HOLDINGS ALUQN AMYDB ASPBG AVWKF AZFZN AZVAB BDRZF BFHJK BMXJE BRXPI BSCLL DCZOG DRFUL DRSTM DU5 EBS EJD ESX FEDTE G-S GODZA HGLYW HVGLF HZ~ I-F LATKE LEEKS LH4 LITHE LOXES LUTES LW6 LYRES MEWTI MXFUL MXSTM MY~ NNB O9- P2W P4E ROL SUPJJ TUS WBKPD WOHZO WXSBR WYJ XV2 ZZTAW AAHQN AAMNL AANHP AAYCA ACRPL ACUHS ACYXJ ADNMO AFWVQ ALVPJ AAMMB AEFGJ AEYWJ AGQPQ AGXDD AGYGG AIDQK AIDYY |
| ID | FETCH-LOGICAL-i3705-9dbeec94f5bc73519b86f348606d612d2cbeec169c9be4028f4b0247d7ddc8a3 |
| ISSN | 1867-3880 |
| IngestDate | Fri Jul 25 12:12:00 EDT 2025 Wed Jan 22 16:30:39 EST 2025 Wed Oct 30 09:49:09 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 10 |
| Language | English |
| LinkModel | OpenURL |
| MergedId | FETCHMERGED-LOGICAL-i3705-9dbeec94f5bc73519b86f348606d612d2cbeec169c9be4028f4b0247d7ddc8a3 |
| Notes | ArticleID:CCTC201402415 ark:/67375/WNG-1XF04JV3-Q istex:216294D0801425EA2B50EC4C56D4DC226141038E National Natural Science Foundation of China (NNSFC) - No. 21272053; No. 21072042 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
| PQID | 1586124935 |
| PQPubID | 986343 |
| PageCount | 6 |
| ParticipantIDs | proquest_journals_1586124935 wiley_primary_10_1002_cctc_201402415_CCTC201402415 istex_primary_ark_67375_WNG_1XF04JV3_Q |
| PublicationCentury | 2000 |
| PublicationDate | October 2014 |
| PublicationDateYYYYMMDD | 2014-10-01 |
| PublicationDate_xml | – month: 10 year: 2014 text: October 2014 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim |
| PublicationTitle | ChemCatChem |
| PublicationTitleAlternate | ChemCatChem |
| PublicationYear | 2014 |
| Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley Subscription Services, Inc |
| References | S. R. Kale, S. S. Kahandal, M. B. Gawande, R. V. Jayaram, RSC Adv. 2013, 3, 8184-8192 J. M. Chezal, J. Paeshuyse, V. Gaumet, D. Canitrot, A. Maisonial, C. Lartigue, A. Gueiffier, E. Moreau, J. C. Teulade, O. Chavignon, J. Neyts, Eur. J. Med. Chem. 2010, 45, 2044-2047. R. R. Jella, R. Nagarajan, Tetrahedron 2013, 69, 10249-10253 N. Chernyak, V. Gevorgyan, Angew. Chem. Int. Ed. 2010, 49, 2743-2746 M. H. Li, Y. L. Gu, Adv. Synth. Catal. 2012, 354, 2484-2494 B. L. Li, M. Zhang, H. C. Hu, X. Du, Z. H. Zhang, New J. Chem. 2014, 38, 2435-2442. M. J. Jacinto, F. P. Silva, P. K. Kiyohara, R. Landers, L. M. Rossi, ChemCatChem 2012, 4, 698-703 R. Z. Zhang, C. X. Miao, S. F. Wang, C. G. Xia, W. Sun, ChemCatChem 2012, 4, 192-195 J. Yang, H. Q. Li, M. H. Li, J. J. Peng, Y. L. Gu, Adv. Synth. Catal. 2012, 354, 688-700 P. H. Li, B. L. Li, Z. M. An, L. P. Mo, Z. S. Cui, Z. H. Zhang, Adv. Synth. Catal. 2013, 355, 2952-2959 T. Sanaeishoar, H. Tavakkoli, F. Mohave, Appl. Catal. A 2014, 470, 56-62. S. Gore, S. Baskaran, B. König, Org. Lett. 2012, 14, 4568-4571 B. L. Li, P. H. Li, X. N. Fang, C. X. Li, J. L. Sun, L. P. Mo, Z. H. Zhang, Tetrahedron 2013, 69, 7011-7018 T. Palani, K. Park, M. R. Kumar, H. M. Jung, S. Lee, Eur. J. Org. Chem. 2012, 5038-5047. H. Y. Chen, J. H. Wu, Appl. Surf. Sci. 2012, 258, 4844-4847 Z. H. Zhang, X. N. Zhang, L. P. Mo, Y. X. Li, F. P. Ma, Green Chem. 2012, 14, 1502-1506. K. B. Puttaraju, K. Shivashankar, RSC Adv. 2013, 3, 20883-20890. P. H. Li, B. L. Li, H. C. Hu, X. N. Zhao, Z. H. Zhang, Catal. Commun. 2014, 46, 118-122 A. S. Burange, S. R. Kale, R. Zboril, M. B. Gawande, R. V. Jayaram, RSC Adv. 2014, 4, 6597-6601 T. Guntreddi, B. K. Allam, K. N. Singh, Synlett 2012, 2635-2638. X. N. Zhang, Y. X. Li, Z. H. Zhang, Tetrahedron 2011, 67, 7426-7430 D. Firmansyah, A. I. Ciuciu, V. Hugues, M. Blanchard-Desce, L. Flamigni, D. T. Gryko, Chem. Asian J. 2013, 8, 1279-1294. P. Liu, C. L. Deng, X. S. Lei, G. Q. Lin, Eur. J. Org. Chem. 2011, 7308-7316. B. V. S. Reddy, P. S. Reddy, Y. J. Reddy, J. S. Yadav, Tetrahedron Lett. 2011, 52, 5789-5793. H. J. Xu, X. Wan, Y. Geng, X. L. Xu, Curr. Org. Chem. 2013, 17, 1034-1050. A. Martínez-Asencio, M. Yus, D. J. Ramón, Tetrahedron 2012, 68, 3948-3951 D. Chandra Mohan, S. N. Rao, S. Adimurthy, J. Org. Chem. 2013, 78, 1266-1272. L. R. Wen, T. He, M. C. Lan, M. Li, J. Org. Chem. 2013, 78, 10617-10628 M. Li, X. L. Lv, L. R. Wen, Z. Q. Hu, Org. Lett. 2013, 15, 1262-1265 J. Patzsch, I. Balog, P. Krauβ, C. W. Lehmann, J. J. Schneider, RSC Adv. 2014, 4, 15348-15355. I. Hawkins, S. T. Handy, Tetrahedron 2013, 69, 9200-9204 F. P. Ma, P. H. Li, B. L. Li, L. P. Mo, N. Liu, H. J. Kang, Y. N. Liu, Z. H. Zhang, Appl. Catal. A 2013, 457, 34-41 R. Y. Guo, P. Wang, G. D. Wang, L. P. Mo, Z. H. Zhang, Tetrahedron 2013, 69, 2056-2061 M. B. Gawande, A. K. Rathi, I. D. Nogueira, R. S. Varma, P. S. Branco, Green Chem. 2013, 15, 1895-1899 C. He, J. Hao, H. Xu, Y. P. Mo, H. Y. Liu, J. J. Han, A. W. Lei, Chem. Commun. 2012, 48, 11073-11075. A. T. Nguyen, L. T. M. Nguyen, C. K. Nguyen, T. Truong, N. T. S. Phan, ChemCatChem 2014, 6, 815-823. M. B. Gawande, V. D. B. Bonifacio, R. S. Varma, I. D. Nogueira, N. Bundaleski, C. A. A. Ghumman, O. Teodoro, P. S. Branco, Green Chem. 2013, 15, 1226-1231 J. T. Hou, J. W. Gao, Z. H. Zhang, Appl. Organomet. Chem. 2011, 25, 47-53 I. R. Siddiqui, P. Rai, Rahila, A. Srivastava, S. Shamim, Tetrahedron Lett. 2014, 55, 1159-1163. S. Mishra, R. Ghosh, Synthesis 2011, 3463-3470. M. B. Gawande, A. Rathi, I. D. Nogueira, C. A. A. Ghumman, N. Bundaleski, O. Teodoro, P. S. Branco, ChemPlusChem 2012, 77, 865-871 Q. H. Zhang, K. D. Vigier, S. Royer, F. Jerome, Chem. Soc. Rev. 2012, 41, 7108-7146 T. H. Al-Tel, R. A. Al-Qawasmeh, R. Zaarour, Eur. J. Med. Chem. 2011, 46, 1874-1881. Angew. Chem. 2010, 122, 2803-2806. S. Kazemi Movahed, M. Dabiri, A. Bazgir, Helv. Chim. Acta 2013, 96, 525-532. R. L. Yan, H. Yan, C. Ma, Z. Y. Ren, X. A. Gao, G. S. Huang, Y. M. Liang, J. Org. Chem. 2012, 77, 2024-2028. F. P. Ma, G. T. Cheng, Z. G. He, Z. H. Zhang, Aust. J. Chem. 2012, 65, 409-416 R. Cano, J. M. Perez, D. J. Ramón, Appl. Catal. A 2014, 470, 177-182 X. N. Zhao, H. C. Hu, F. J. Zhang, Z. H. Zhang, Appl. Catal. A 2014, 482, 258-265. J. Deng, L. P. Mo, F. Y. Zhao, L. L. Hou, L. Yang, Z. H. Zhang, Green Chem. 2011, 13, 2576-2584 U. B. Patil, S. S. Shendage, J. M. Nagarkar, Synthesis 2013, 45, 3295-3299. Y. L. Gu, F. Jerome, Chem. Soc. Rev. 2013, 42, 9550-9570. H. Cao, X. H. Liu, L. M. Zhao, J. H. Cen, J. X. Lin, Q. X. Zhu, M. L. Fu, Org. Lett. 2014, 16, 146-149. S. Bassaid, M. Chaib, S. Omeiri, A. Bouguelia, M. Trari, J. Photochem. Photobiol. A 2009, 201, 62-68 J. Sun, D. Zhu, H. Gong, C. G. Yan, Tetrahedron 2013, 69, 10565-10572. R. Mrowczynski, A. Nan, J. Liebscher, RSC Adv. 2014, 4, 5927-5952 Y. H. Liu, J. Deng, J. W. Gao, Z. H. Zhang, Adv. Synth. Catal. 2012, 354, 441-447 H. Zhu, X. X. Jiang, X. H. Li, C. Hou, Y. Jiang, K. Hou, R. Wang, Y. F. Li, ChemCatChem 2013, 5, 2187-2190 P. Liu, L. S. Fang, X. S. Lei, G. Q. Lin, Tetrahedron Lett. 2010, 51, 4605-4608. B. Karimi, H. M. Mirzaei, E. Farhangi, ChemCatChem 2014, 6, 758-762 S. Ulloora, R. Shabaraya, A. V. Adhikari, Bioorg. Med. Chem. Lett. 2013, 23, 3368-3372. A. K. Bagdi, M. Rahman, S. Santra, A. Majee, A. Hajra, Adv. Synth. Catal. 2013, 355, 1741-1747. C. Russ, B. Konig, Green Chem. 2012, 14, 2969-2982 R. Ducray, C. D. Jones, F. H. Jung, I. Simpson, J. Curwen, M. Pass, Bioorg. Med. Chem. Lett. 2011, 21, 4702-4704. G. C. Moraski, L. D. Markley, P. A. Hipskind, H. Boshoff, S. Cho, S. G. Franzblau, M. J. Miller, ACS Med. Chem. Lett. 2011, 2, 466-470. R. Y. Guo, Z. M. An, L. P. Mo, R. Z. Wang, H. X. Liu, S. X. Wang, Z. H. Zhang, ACS Comb. Sci. 2013, 15, 557-563. M. B. Gawande, P. S. Branco, R. S. Varma, Chem. Soc. Rev. 2013, 42, 3371-3393 J. Zeng, Y. J. Tan, M. L. Leow, X. W. Liu, Org. Lett. 2012, 14, 4386-4389. R. Y. Guo, Z. M. An, L. P. Mo, S. T. Yang, H. X. Liu, S. X. Wang, Z. H. Zhang, Tetrahedron 2013, 69, 9931-9938 T. Mitsudome, K. Kaneda, ChemCatChem 2013, 5, 1681-1691 R. Cano, M. Yus, D. J. Ramón, Tetrahedron 2013, 69, 7056-7065 J. Deng, L. P. Mo, F. Y. Zhao, Z. H. Zhang, S. X. Liu, ACS Comb. Sci. 2012, 14, 335-341 Y. Terao, H. Suzuki, M. Yoshikawa, H. Yashiro, S. Takekawa, Y. Fujitani, K. Okada, Y. Inoue, Y. Yamamoto, H. Nakagawa, S. H. Yao, T. Kawamoto, O. Uchikawa, Bioorg. Med. Chem. Lett. 2012, 22, 7326-7329. S. Gore, K. Chinthapally, S. Baskaran, B. König, Chem. Commun. 2013, 49, 5052-5054 M. B. Gawande, P. S. Branco, I. D. Nogueira, C. A. A. Ghumman, N. Bundaleski, A. Santos, O. Teodoro, R. Luque, Green Chem. 2013, 15, 682-689 M. H. Li, A. Taheri, M. Liu, S. H. Sun, Y. L. Gu, Adv. Synth. Catal. 2014, 356, 537-556 A. Rajawat, S. Khandelwal, M. Kumar, RSC Adv. 2014, 4, 5105-5112 C. Vidal, F. J. Suarez, J. Garcia-Alvarez, Catal. Commun. 2014, 44, 76-79 M. B. Gawande, H. Z. Guo, A. K. Rathi, P. S. Branco, Y. Z. Chen, R. S. Varma, D. L. Peng, RSC Adv. 2013, 3, 1050-1054 K. Guchhait, A. L. Chandgude, G. Priyadarshani, J. Org. Chem. 2012, 77, 4438-4444. P. H. Li, F. P. Ma, P. Wang, Z. H. Zhang, Chin. J. Chem. 2013, 31, 757-763 H. Mahmoudi, A. A. Jafari, ChemCatChem 2013, 5, 3743-3749 T. Yang, H. Cui, C. H. Zhang, L. Zhang, C. Y. Su, ChemCatChem 2013, 5, 3131-3138. G. C. Moraski, L. D. Markley, M. Chang, S. Cho, S. G. Franzblau, C. H. Hwang, H. Boshoff, M. J. Miller, Bioorg. Med. Chem. 2012, 20, 2214-2220. T. H. Al-Tel, R. A. Al-Qawasmeh, Eur. J. Med. Chem. 2010, 45, 5848-5855. S. Matsumoto, N. Miyamoto, T. Hirayama, H. Oki, K. Okada, M. Tawada, H. Iwata, K. Nakamura, S. Yamasaki, H. Miki, A. Hori, S. Imamura, Bioorg. Med. Chem. 2013, 21, 7686-7698. B. L. Li, H. C. Hu, L. P. Mo, Z. H. Zhang, RSC Adv. 2014, 4, 12929-12943 2013; 3 2013; 69 2013; 21 2013; 23 2011; 52 2011; 13 2012; 14 2013; 8 2013; 5 2013; 15 2014; 4 2013; 17 2013; 96 2014; 16 2011; 21 2013; 355 2009; 201 2011; 67 2011; 25 2012; 68 2012; 258 2014; 482 2014; 6 2012; 22 2012; 65 2012; 20 2014; 55 2011; 2 2013; 49 2012 2011 2013; 45 2013; 42 2014; 46 2010 2010; 49 122 2014; 470 2012; 77 2014; 356 2014; 44 2010; 45 2012; 354 2013; 78 2013; 457 2013; 31 2014; 38 2011; 46 2012; 48 2012; 4 2010; 51 2012; 41 |
| References_xml | – reference: S. Matsumoto, N. Miyamoto, T. Hirayama, H. Oki, K. Okada, M. Tawada, H. Iwata, K. Nakamura, S. Yamasaki, H. Miki, A. Hori, S. Imamura, Bioorg. Med. Chem. 2013, 21, 7686-7698. – reference: H. Cao, X. H. Liu, L. M. Zhao, J. H. Cen, J. X. Lin, Q. X. Zhu, M. L. Fu, Org. Lett. 2014, 16, 146-149. – reference: M. H. Li, A. Taheri, M. Liu, S. H. Sun, Y. L. Gu, Adv. Synth. Catal. 2014, 356, 537-556; – reference: G. C. Moraski, L. D. Markley, M. Chang, S. Cho, S. G. Franzblau, C. H. Hwang, H. Boshoff, M. J. Miller, Bioorg. Med. Chem. 2012, 20, 2214-2220. – reference: S. Gore, K. Chinthapally, S. Baskaran, B. König, Chem. Commun. 2013, 49, 5052-5054; – reference: R. Cano, J. M. Perez, D. J. Ramón, Appl. Catal. A 2014, 470, 177-182; – reference: X. N. Zhang, Y. X. Li, Z. H. Zhang, Tetrahedron 2011, 67, 7426-7430; – reference: D. Firmansyah, A. I. Ciuciu, V. Hugues, M. Blanchard-Desce, L. Flamigni, D. T. Gryko, Chem. Asian J. 2013, 8, 1279-1294. – reference: B. L. Li, H. C. Hu, L. P. Mo, Z. H. Zhang, RSC Adv. 2014, 4, 12929-12943; – reference: R. Ducray, C. D. Jones, F. H. Jung, I. Simpson, J. Curwen, M. Pass, Bioorg. Med. Chem. Lett. 2011, 21, 4702-4704. – reference: F. P. Ma, P. H. Li, B. L. Li, L. P. Mo, N. Liu, H. J. Kang, Y. N. Liu, Z. H. Zhang, Appl. Catal. A 2013, 457, 34-41; – reference: T. H. Al-Tel, R. A. Al-Qawasmeh, Eur. J. Med. Chem. 2010, 45, 5848-5855. – reference: S. Ulloora, R. Shabaraya, A. V. Adhikari, Bioorg. Med. Chem. Lett. 2013, 23, 3368-3372. – reference: R. Y. Guo, P. Wang, G. D. Wang, L. P. Mo, Z. H. Zhang, Tetrahedron 2013, 69, 2056-2061; – reference: A. T. Nguyen, L. T. M. Nguyen, C. K. Nguyen, T. Truong, N. T. S. Phan, ChemCatChem 2014, 6, 815-823. – reference: J. M. Chezal, J. Paeshuyse, V. Gaumet, D. Canitrot, A. Maisonial, C. Lartigue, A. Gueiffier, E. Moreau, J. C. Teulade, O. Chavignon, J. Neyts, Eur. J. Med. Chem. 2010, 45, 2044-2047. – reference: R. Y. Guo, Z. M. An, L. P. Mo, S. T. Yang, H. X. Liu, S. X. Wang, Z. H. Zhang, Tetrahedron 2013, 69, 9931-9938; – reference: M. Li, X. L. Lv, L. R. Wen, Z. Q. Hu, Org. Lett. 2013, 15, 1262-1265; – reference: K. Guchhait, A. L. Chandgude, G. Priyadarshani, J. Org. Chem. 2012, 77, 4438-4444. – reference: J. Zeng, Y. J. Tan, M. L. Leow, X. W. Liu, Org. Lett. 2012, 14, 4386-4389. – reference: F. P. Ma, G. T. Cheng, Z. G. He, Z. H. Zhang, Aust. J. Chem. 2012, 65, 409-416; – reference: T. Palani, K. Park, M. R. Kumar, H. M. Jung, S. Lee, Eur. J. Org. Chem. 2012, 5038-5047. – reference: K. B. Puttaraju, K. Shivashankar, RSC Adv. 2013, 3, 20883-20890. – reference: M. B. Gawande, A. Rathi, I. D. Nogueira, C. A. A. Ghumman, N. Bundaleski, O. Teodoro, P. S. Branco, ChemPlusChem 2012, 77, 865-871; – reference: L. R. Wen, T. He, M. C. Lan, M. Li, J. Org. Chem. 2013, 78, 10617-10628; – reference: S. Kazemi Movahed, M. Dabiri, A. Bazgir, Helv. Chim. Acta 2013, 96, 525-532. – reference: T. Guntreddi, B. K. Allam, K. N. Singh, Synlett 2012, 2635-2638. – reference: B. L. Li, P. H. Li, X. N. Fang, C. X. Li, J. L. Sun, L. P. Mo, Z. H. Zhang, Tetrahedron 2013, 69, 7011-7018; – reference: X. N. Zhao, H. C. Hu, F. J. Zhang, Z. H. Zhang, Appl. Catal. A 2014, 482, 258-265. – reference: S. Bassaid, M. Chaib, S. Omeiri, A. Bouguelia, M. Trari, J. Photochem. Photobiol. A 2009, 201, 62-68; – reference: I. Hawkins, S. T. Handy, Tetrahedron 2013, 69, 9200-9204; – reference: M. B. Gawande, A. K. Rathi, I. D. Nogueira, R. S. Varma, P. S. Branco, Green Chem. 2013, 15, 1895-1899; – reference: R. Z. Zhang, C. X. Miao, S. F. Wang, C. G. Xia, W. Sun, ChemCatChem 2012, 4, 192-195; – reference: S. Gore, S. Baskaran, B. König, Org. Lett. 2012, 14, 4568-4571; – reference: A. Martínez-Asencio, M. Yus, D. J. Ramón, Tetrahedron 2012, 68, 3948-3951; – reference: P. H. Li, F. P. Ma, P. Wang, Z. H. Zhang, Chin. J. Chem. 2013, 31, 757-763; – reference: C. Vidal, F. J. Suarez, J. Garcia-Alvarez, Catal. Commun. 2014, 44, 76-79; – reference: Angew. Chem. 2010, 122, 2803-2806. – reference: S. Mishra, R. Ghosh, Synthesis 2011, 3463-3470. – reference: P. H. Li, B. L. Li, Z. M. An, L. P. Mo, Z. S. Cui, Z. H. Zhang, Adv. Synth. Catal. 2013, 355, 2952-2959; – reference: H. Zhu, X. X. Jiang, X. H. Li, C. Hou, Y. Jiang, K. Hou, R. Wang, Y. F. Li, ChemCatChem 2013, 5, 2187-2190; – reference: R. Cano, M. Yus, D. J. Ramón, Tetrahedron 2013, 69, 7056-7065; – reference: A. K. Bagdi, M. Rahman, S. Santra, A. Majee, A. Hajra, Adv. Synth. Catal. 2013, 355, 1741-1747. – reference: J. T. Hou, J. W. Gao, Z. H. Zhang, Appl. Organomet. Chem. 2011, 25, 47-53; – reference: U. B. Patil, S. S. Shendage, J. M. Nagarkar, Synthesis 2013, 45, 3295-3299. – reference: Y. Terao, H. Suzuki, M. Yoshikawa, H. Yashiro, S. Takekawa, Y. Fujitani, K. Okada, Y. Inoue, Y. Yamamoto, H. Nakagawa, S. H. Yao, T. Kawamoto, O. Uchikawa, Bioorg. Med. Chem. Lett. 2012, 22, 7326-7329. – reference: B. Karimi, H. M. Mirzaei, E. Farhangi, ChemCatChem 2014, 6, 758-762; – reference: A. S. Burange, S. R. Kale, R. Zboril, M. B. Gawande, R. V. Jayaram, RSC Adv. 2014, 4, 6597-6601; – reference: J. Sun, D. Zhu, H. Gong, C. G. Yan, Tetrahedron 2013, 69, 10565-10572. – reference: R. L. Yan, H. Yan, C. Ma, Z. Y. Ren, X. A. Gao, G. S. Huang, Y. M. Liang, J. Org. Chem. 2012, 77, 2024-2028. – reference: S. R. Kale, S. S. Kahandal, M. B. Gawande, R. V. Jayaram, RSC Adv. 2013, 3, 8184-8192; – reference: R. Mrowczynski, A. Nan, J. Liebscher, RSC Adv. 2014, 4, 5927-5952; – reference: B. L. Li, M. Zhang, H. C. Hu, X. Du, Z. H. Zhang, New J. Chem. 2014, 38, 2435-2442. – reference: T. Sanaeishoar, H. Tavakkoli, F. Mohave, Appl. Catal. A 2014, 470, 56-62. – reference: Y. L. Gu, F. Jerome, Chem. Soc. Rev. 2013, 42, 9550-9570. – reference: Z. H. Zhang, X. N. Zhang, L. P. Mo, Y. X. Li, F. P. Ma, Green Chem. 2012, 14, 1502-1506. – reference: R. R. Jella, R. Nagarajan, Tetrahedron 2013, 69, 10249-10253; – reference: M. B. Gawande, P. S. Branco, R. S. Varma, Chem. Soc. Rev. 2013, 42, 3371-3393; – reference: P. H. Li, B. L. Li, H. C. Hu, X. N. Zhao, Z. H. Zhang, Catal. Commun. 2014, 46, 118-122; – reference: J. Deng, L. P. Mo, F. Y. Zhao, L. L. Hou, L. Yang, Z. H. Zhang, Green Chem. 2011, 13, 2576-2584; – reference: D. Chandra Mohan, S. N. Rao, S. Adimurthy, J. Org. Chem. 2013, 78, 1266-1272. – reference: P. Liu, L. S. Fang, X. S. Lei, G. Q. Lin, Tetrahedron Lett. 2010, 51, 4605-4608. – reference: Y. H. Liu, J. Deng, J. W. Gao, Z. H. Zhang, Adv. Synth. Catal. 2012, 354, 441-447; – reference: H. J. Xu, X. Wan, Y. Geng, X. L. Xu, Curr. Org. Chem. 2013, 17, 1034-1050. – reference: M. B. Gawande, V. D. B. Bonifacio, R. S. Varma, I. D. Nogueira, N. Bundaleski, C. A. A. Ghumman, O. Teodoro, P. S. Branco, Green Chem. 2013, 15, 1226-1231; – reference: I. R. Siddiqui, P. Rai, Rahila, A. Srivastava, S. Shamim, Tetrahedron Lett. 2014, 55, 1159-1163. – reference: H. Y. Chen, J. H. Wu, Appl. Surf. Sci. 2012, 258, 4844-4847; – reference: G. C. Moraski, L. D. Markley, P. A. Hipskind, H. Boshoff, S. Cho, S. G. Franzblau, M. J. Miller, ACS Med. Chem. Lett. 2011, 2, 466-470. – reference: M. J. Jacinto, F. P. Silva, P. K. Kiyohara, R. Landers, L. M. Rossi, ChemCatChem 2012, 4, 698-703; – reference: A. Rajawat, S. Khandelwal, M. Kumar, RSC Adv. 2014, 4, 5105-5112; – reference: T. Mitsudome, K. Kaneda, ChemCatChem 2013, 5, 1681-1691; – reference: M. B. Gawande, P. S. Branco, I. D. Nogueira, C. A. A. Ghumman, N. Bundaleski, A. Santos, O. Teodoro, R. Luque, Green Chem. 2013, 15, 682-689; – reference: Q. H. Zhang, K. D. Vigier, S. Royer, F. Jerome, Chem. Soc. Rev. 2012, 41, 7108-7146; – reference: J. Yang, H. Q. Li, M. H. Li, J. J. Peng, Y. L. Gu, Adv. Synth. Catal. 2012, 354, 688-700; – reference: M. B. Gawande, H. Z. Guo, A. K. Rathi, P. S. Branco, Y. Z. Chen, R. S. Varma, D. L. Peng, RSC Adv. 2013, 3, 1050-1054; – reference: H. Mahmoudi, A. A. Jafari, ChemCatChem 2013, 5, 3743-3749; – reference: T. H. Al-Tel, R. A. Al-Qawasmeh, R. Zaarour, Eur. J. Med. Chem. 2011, 46, 1874-1881. – reference: C. He, J. Hao, H. Xu, Y. P. Mo, H. Y. Liu, J. J. Han, A. W. Lei, Chem. Commun. 2012, 48, 11073-11075. – reference: B. V. S. Reddy, P. S. Reddy, Y. J. Reddy, J. S. Yadav, Tetrahedron Lett. 2011, 52, 5789-5793. – reference: J. Patzsch, I. Balog, P. Krauβ, C. W. Lehmann, J. J. Schneider, RSC Adv. 2014, 4, 15348-15355. – reference: N. Chernyak, V. Gevorgyan, Angew. Chem. Int. Ed. 2010, 49, 2743-2746; – reference: C. Russ, B. Konig, Green Chem. 2012, 14, 2969-2982; – reference: J. Deng, L. P. Mo, F. Y. Zhao, Z. H. Zhang, S. X. Liu, ACS Comb. Sci. 2012, 14, 335-341; – reference: P. Liu, C. L. Deng, X. S. Lei, G. Q. Lin, Eur. J. Org. Chem. 2011, 7308-7316. – reference: M. H. Li, Y. L. Gu, Adv. Synth. Catal. 2012, 354, 2484-2494; – reference: T. Yang, H. Cui, C. H. Zhang, L. Zhang, C. Y. Su, ChemCatChem 2013, 5, 3131-3138. – reference: R. Y. Guo, Z. M. An, L. P. Mo, R. Z. Wang, H. X. Liu, S. X. Wang, Z. H. Zhang, ACS Comb. Sci. 2013, 15, 557-563. – volume: 354 start-page: 441 year: 2012 end-page: 447 publication-title: Adv. Synth. Catal. – volume: 4 start-page: 5105 year: 2014 end-page: 5112 publication-title: RSC Adv. – volume: 69 start-page: 10249 year: 2013 end-page: 10253 publication-title: Tetrahedron – volume: 482 start-page: 258 year: 2014 end-page: 265 publication-title: Appl. Catal. A – volume: 38 start-page: 2435 year: 2014 end-page: 2442 publication-title: New J. Chem. – volume: 42 start-page: 9550 year: 2013 end-page: 9570 publication-title: Chem. Soc. Rev. – volume: 67 start-page: 7426 year: 2011 end-page: 7430 publication-title: Tetrahedron – volume: 470 start-page: 56 year: 2014 end-page: 62 publication-title: Appl. Catal. A – volume: 355 start-page: 2952 year: 2013 end-page: 2959 publication-title: Adv. Synth. Catal. – volume: 23 start-page: 3368 year: 2013 end-page: 3372 publication-title: Bioorg. Med. Chem. Lett. – volume: 78 start-page: 1266 year: 2013 end-page: 1272 publication-title: J. Org. Chem. – volume: 13 start-page: 2576 year: 2011 end-page: 2584 publication-title: Green Chem. – volume: 15 start-page: 1226 year: 2013 end-page: 1231 publication-title: Green Chem. – volume: 45 start-page: 2044 year: 2010 end-page: 2047 publication-title: Eur. J. Med. Chem. – volume: 5 start-page: 3131 year: 2013 end-page: 3138 publication-title: ChemCatChem – volume: 55 start-page: 1159 year: 2014 end-page: 1163 publication-title: Tetrahedron Lett. – volume: 48 start-page: 11073 year: 2012 end-page: 11075 publication-title: Chem. Commun. – volume: 15 start-page: 682 year: 2013 end-page: 689 publication-title: Green Chem. – volume: 77 start-page: 4438 year: 2012 end-page: 4444 publication-title: J. Org. Chem. – volume: 22 start-page: 7326 year: 2012 end-page: 7329 publication-title: Bioorg. Med. Chem. Lett. – volume: 3 start-page: 20883 year: 2013 end-page: 20890 publication-title: RSC Adv. – volume: 4 start-page: 12929 year: 2014 end-page: 12943 publication-title: RSC Adv. – volume: 21 start-page: 4702 year: 2011 end-page: 4704 publication-title: Bioorg. Med. Chem. Lett. – volume: 96 start-page: 525 year: 2013 end-page: 532 publication-title: Helv. Chim. Acta – volume: 2 start-page: 466 year: 2011 end-page: 470 publication-title: ACS Med. Chem. Lett. – volume: 68 start-page: 3948 year: 2012 end-page: 3951 publication-title: Tetrahedron – volume: 15 start-page: 1895 year: 2013 end-page: 1899 publication-title: Green Chem. – volume: 45 start-page: 3295 year: 2013 end-page: 3299 publication-title: Synthesis – volume: 356 start-page: 537 year: 2014 end-page: 556 publication-title: Adv. Synth. Catal. – volume: 4 start-page: 15348 year: 2014 end-page: 15355 publication-title: RSC Adv. – volume: 42 start-page: 3371 year: 2013 end-page: 3393 publication-title: Chem. Soc. Rev. – volume: 5 start-page: 3743 year: 2013 end-page: 3749 publication-title: ChemCatChem – volume: 52 start-page: 5789 year: 2011 end-page: 5793 publication-title: Tetrahedron Lett. – volume: 14 start-page: 335 year: 2012 end-page: 341 publication-title: ACS Comb. Sci. – volume: 77 start-page: 2024 year: 2012 end-page: 2028 publication-title: J. Org. Chem. – volume: 470 start-page: 177 year: 2014 end-page: 182 publication-title: Appl. Catal. A – volume: 20 start-page: 2214 year: 2012 end-page: 2220 publication-title: Bioorg. Med. Chem. – volume: 14 start-page: 4386 year: 2012 end-page: 4389 publication-title: Org. Lett. – volume: 69 start-page: 9200 year: 2013 end-page: 9204 publication-title: Tetrahedron – volume: 78 start-page: 10617 year: 2013 end-page: 10628 publication-title: J. Org. Chem. – volume: 69 start-page: 10565 year: 2013 end-page: 10572 publication-title: Tetrahedron – volume: 4 start-page: 6597 year: 2014 end-page: 6601 publication-title: RSC Adv. – volume: 4 start-page: 698 year: 2012 end-page: 703 publication-title: ChemCatChem – volume: 65 start-page: 409 year: 2012 end-page: 416 publication-title: Aust. J. Chem. – volume: 5 start-page: 1681 year: 2013 end-page: 1691 publication-title: ChemCatChem – volume: 6 start-page: 758 year: 2014 end-page: 762 publication-title: ChemCatChem – volume: 41 start-page: 7108 year: 2012 end-page: 7146 publication-title: Chem. Soc. Rev. – volume: 3 start-page: 8184 year: 2013 end-page: 8192 publication-title: RSC Adv. – volume: 69 start-page: 7011 year: 2013 end-page: 7018 publication-title: Tetrahedron – volume: 21 start-page: 7686 year: 2013 end-page: 7698 publication-title: Bioorg. Med. Chem. – volume: 354 start-page: 2484 year: 2012 end-page: 2494 publication-title: Adv. Synth. Catal. – volume: 46 start-page: 1874 year: 2011 end-page: 1881 publication-title: Eur. J. Med. Chem. – volume: 16 start-page: 146 year: 2014 end-page: 149 publication-title: Org. Lett. – volume: 4 start-page: 5927 year: 2014 end-page: 5952 publication-title: RSC Adv. – volume: 49 start-page: 5052 year: 2013 end-page: 5054 publication-title: Chem. Commun. – volume: 51 start-page: 4605 year: 2010 end-page: 4608 publication-title: Tetrahedron Lett. – volume: 201 start-page: 62 year: 2009 end-page: 68 publication-title: J. Photochem. Photobiol. A – volume: 31 start-page: 757 year: 2013 end-page: 763 publication-title: Chin. J. Chem. – volume: 354 start-page: 688 year: 2012 end-page: 700 publication-title: Adv. Synth. Catal. – volume: 49 122 start-page: 2743 2803 year: 2010 2010 end-page: 2746 2806 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 17 start-page: 1034 year: 2013 end-page: 1050 publication-title: Curr. Org. Chem. – volume: 355 start-page: 1741 year: 2013 end-page: 1747 publication-title: Adv. Synth. Catal. – volume: 69 start-page: 2056 year: 2013 end-page: 2061 publication-title: Tetrahedron – volume: 69 start-page: 7056 year: 2013 end-page: 7065 publication-title: Tetrahedron – volume: 5 start-page: 2187 year: 2013 end-page: 2190 publication-title: ChemCatChem – volume: 258 start-page: 4844 year: 2012 end-page: 4847 publication-title: Appl. Surf. Sci. – volume: 46 start-page: 118 year: 2014 end-page: 122 publication-title: Catal. Commun. – volume: 15 start-page: 1262 year: 2013 end-page: 1265 publication-title: Org. Lett. – volume: 14 start-page: 1502 year: 2012 end-page: 1506 publication-title: Green Chem. – volume: 8 start-page: 1279 year: 2013 end-page: 1294 publication-title: Chem. Asian J. – start-page: 7308 year: 2011 end-page: 7316 publication-title: Eur. J. Org. Chem. – volume: 6 start-page: 815 year: 2014 end-page: 823 publication-title: ChemCatChem – volume: 3 start-page: 1050 year: 2013 end-page: 1054 publication-title: RSC Adv. – volume: 69 start-page: 9931 year: 2013 end-page: 9938 publication-title: Tetrahedron – volume: 4 start-page: 192 year: 2012 end-page: 195 publication-title: ChemCatChem – start-page: 2635 year: 2012 end-page: 2638 publication-title: Synlett – volume: 457 start-page: 34 year: 2013 end-page: 41 publication-title: Appl. Catal. A – volume: 15 start-page: 557 year: 2013 end-page: 563 publication-title: ACS Comb. Sci. – volume: 14 start-page: 4568 year: 2012 end-page: 4571 publication-title: Org. Lett. – start-page: 5038 year: 2012 end-page: 5047 publication-title: Eur. J. Org. Chem. – volume: 14 start-page: 2969 year: 2012 end-page: 2982 publication-title: Green Chem. – volume: 44 start-page: 76 year: 2014 end-page: 79 publication-title: Catal. Commun. – volume: 45 start-page: 5848 year: 2010 end-page: 5855 publication-title: Eur. J. Med. Chem. – volume: 25 start-page: 47 year: 2011 end-page: 53 publication-title: Appl. Organomet. Chem. – start-page: 3463 year: 2011 end-page: 3470 publication-title: Synthesis – volume: 77 start-page: 865 year: 2012 end-page: 871 publication-title: ChemPlusChem |
| SSID | ssj0069375 |
| Score | 2.4254665 |
| Snippet | Superparamagnetic CuFeO2 nanoparticles were prepared and characterized by XRD, SEM, TEM, FRIR spectroscopy, and vibrating sample magnetometry techniques. The... |
| SourceID | proquest wiley istex |
| SourceType | Aggregation Database Publisher |
| StartPage | 2854 |
| SubjectTerms | copper heterocycles iron magnetic properties multicomponent reactions Nanoparticles |
| Title | Superparamagnetic CuFeO2 Nanoparticles in Deep Eutectic Solvent: an Efficient and Recyclable Catalytic System for the Synthesis of Imidazo[1,2-a]pyridines |
| URI | https://api.istex.fr/ark:/67375/WNG-1XF04JV3-Q/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcctc.201402415 https://www.proquest.com/docview/1586124935 |
| Volume | 6 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLaq7gFeEFdRGMgPjJcRSJ07b2vaMqZdmJpBJTRZieOgii2pSoPofgr_if_EObGTphpCg5ekcRpX9fl8Ls7xdwh5kfkuVikShgvGx7CZFAaWyDGSwGTCSiwwmbh3-OjY3T-zD6bOtNP51cpaKpfJa3H1x30l_yNVaAO54i7Zf5Bs0yk0wGeQLxxBwnC8kYwn5VwukLz7Mv6S427E3bAcyxOGOhOCYZ3zhksaQynnu6MS3xjAtybFxXe9KAjTe1SxSNS55uBHrsRFtaEqxKWdVfVAxffcpCROVjmcNJXJ-8tZGl8VO84AlGLIjHjHGc5Xi1mKCfVt3xe5CaBLPDVpQKXaGbLOC6qSC6azuDCiWBvVar1c6WzjtIXmo0ItKhgfavOrVy_6dpMHd1Md2dLNPuh05K5Rpqvdpmos1QrdbePWbGtnXxFWXzMbioZWiIrUEkJOdGvWBrJOCjg-4eOzw0MejabR5l3tDzgM3zoio8EWg6iFdcnW3mA4GNeugQu-IObUNv-kZhE12ZvNH4dQCWf5j424px09Ve5PdJfc0XEL3VOYukc6Mr9PboV1ucAH5Oc1MFIFRroBRjrLKYKR1mCkGoxvaZzTBopwkdI1FGkDRaqgSAGKFDBIGyjSIqMaip_7rwCG5w0IH5JoPIrCfUMX_jBmlmc6RpAmUorAzpxEeFhBMvHdzMJyaW4KHnnKBN6HoRZBImHA_MxOYNi81EtT4cfWI9LNi1w-JlQwE7yvQLBAWjbzsBZBPxGOm8rM9DMme-RlNc58rrhdeLz4iqmOnsM_Hb_j_enYtA8-Wvy0R7ZrQXCtAb7xvuO7WLzdcnqEVcJp-lFs4IyjWHkjVh6GUdhcPfl7n0_J7fWM2Sbd5aKUz8ADXibPNa5-A9svsXA |
| linkProvider | EBSCOhost |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Superparamagnetic+CuFeO2+Nanoparticles+in+Deep+Eutectic+Solvent%3A+an+Efficient+and+Recyclable+Catalytic+System+for+the+Synthesis+of+Imidazo%5B1%2C2-a%5Dpyridines&rft.jtitle=ChemCatChem&rft.au=Lu%2C+Jun&rft.au=Li%2C+Xiao-Tang&rft.au=Ma%2C+Er-Qian&rft.au=Mo%2C+Li-Ping&rft.date=2014-10-01&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=1867-3880&rft.eissn=1867-3899&rft.volume=6&rft.issue=10&rft.spage=2854&rft_id=info:doi/10.1002%2Fcctc.201402415&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=3452516971 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1867-3880&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1867-3880&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1867-3880&client=summon |