Mn(III)-mediated reactions of 2-isocyanobiaryl with 1,3-dicarbonyl compounds: Efficient synthesis of 6-alkylated and 6-monofluoro-alkylated phenanthridines

Chemical Communications

Volumn 50, Issue 85, 2014, Pages 12892-12895

  Cao, Jia Jia ^a   Wang, Xiang ^a   Wang, Shun Yi ^a   Ji, Shun Jun ^a  

^a SOOCHOW UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETOACETIC ACID DERIVATIVE; ALKYL GROUP; CARBONYL DERIVATIVE; MALONIC ACID DERIVATIVE; MANGANESE; PHENANTHRIDINE DERIVATIVE;

ALKYLATION; ARTICLE; CONTROLLED STUDY; DEACETYLATION; DECARBOXYLATION; ELECTRON; HYBRIDIZATION; HYDROGEN BOND; SYNTHESIS; X RAY ANALYSIS; CATALYSIS; CHEMISTRY; HALOGENATION;

ALKYLATION; CATALYSIS; HALOGENATION; MANGANESE; PHENANTHRIDINES;

EID: 84907626260     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc05324a     Document Type: Article

References (38)

1. B. Zhang, C. Mück-Lichtenfeld, C. G. Daniliuc, A. Studer, Angew. Chem., Int. Ed., 2013, 52, 10792
2. Q. Wang, X. Dong, T. Xiao, L. Zhou, Org. Lett., 2013, 15, 4846
3. Y. Cheng, H. Jiang, Y. Zhang, S. Yu, Org. Lett., 2013, 15, 5520
4. D. Leifert, C. G. Daniliuc, A. Studer, Org. Lett., 2013, 15, 6286
5. J. Liu, C. Fan, H. Yin, C. Qin, G. Zhang, X. Zhang, H. Yi, A. Lei, Chem. Commun., 2014, 50, 2145
6. T. Xiao, L. Li, G. Lin, Q. Wang, P. Zhang, Z.-W. Mao, L. Zhou, Green Chem., 2014, 16, 2418
7. L. Gu, C. Jin, J. Liu, H. Ding, B. Fan, Chem. Commun., 2014, 50, 4643
8. B. Zhang, C. G. Daniliuc, A. Studer, Org. Lett., 2014, 16, 250
9. Z. Xia, J. Huang, Y. He, J. Zhao, J. Lei, Q. Zhu, Org. Lett., 2014, 16, 2546
10. B. Yang, Q.-P. Tian, S.-D. Yang, Chin. J. Org. Chem., 2014, 34, 717
11. T. Ishikawa, Med. Res. Rev., 2001, 21, 61
12. W. A. Denny, Curr. Med. Chem., 2002, 9, 1655
13. S. L. Bondarev, V. N. Knyukshto, S. A. Tikhomirov, A. N. Pyrko, Opt. Spectrosc., 2006, 100, 386
14. S. Purser, P. R. Moore, S. Swallow, V. Gouverneur, Chem. Soc. Rev., 2008, 37, 320
15. M. Tobisu, K. Koh, T. Furukawa, N. Chatani, Angew. Chem., Int. Ed., 2012, 51, 11363
16. H. Jiang, Y. Cheng, R. Wang, M. Zheng, Y. Zhang, S. Yu, Angew. Chem., Int. Ed., 2013, 52, 1
17. X. Sun, S. Yu, Org. Lett., 2014, 16, 2938
18. J.-J. Cao, T.-H. Zhu, S.-Y. Wang, Z.-Y. Gu, X. Wang, S.-J. Ji, Chem. Commun., 2014, 50, 6439
19. L. Wang, W. Sha, Q. Dai, X. Feng, W. Wu, H. Peng, B. Chen, J. Cheng, Org. Lett., 2014, 16, 2088
20. W. Sha, J.-T. Yu, Y. Jiang, H. Yang, J. Cheng, Chem. Commun., 2014, 50, 9179
21. Z. Li, F. Fan, J. Yang, Z.-Q. Liu, Org. Lett., 2014, 16, 3396
22. B. B. Snider, Chem. Rev., 1996, 96, 339
23. X.-Q. Pan, J.-P. Zou, W. Zhang, Mol. Diversity, 2009, 13, 421
24. X. Wang, X.-P. Xu, S.-Y. Wang, S.-J. Ji, Org. Lett., 2013, 15, 4246
25. X. Wang, S.-Y. Wang, S.-J. Ji, Org. Lett., 2013, 15, 1954
26. T.-H. Zhu, S.-Y. Wang, G.-N. Wang, S.-J. Ji, Chem. - Eur. J., 2013, 19, 5850
27. L.-L. Zhao, S.-Y. Wang, X.-P. Xu, S.-J. Ji, Chem. Commun., 2013, 49, 2569
28. R. Wang, X.-P. Xu, H. Meng, S.-Y. Wang, S.-J. Ji, Tetrahedron, 2013, 69, 1761
29. R. Wang, S.-Y. Wang, S.-J. Ji, Tetrahedron, 2013, 69, 10836
30. Z.-Y. Gu, T.-H. Zhu, J.-J. Cao, S.-Y. Wang, G.-N. Wang, S.-J. Ji, ACS Catal., 2014, 4, 49
31. P. Song, L.-L. Zhao, S.-J. Ji, Chin. J. Chem., 2014, 32, 381
32. J. V. Greenhill, H. Loghmani-Khouzani, D. J. Maitland, Tetrahedron, 1988, 44, 3319
33. H. Loghmani-Khouzani, R. Gawinecki, M. M. Sadeghi, H. Mehrabi, B. Osmialowski, J. Iran. Chem. Soc., 2005, 2, 294
34. I. V. Alabugin, S. Bresch, M. Manoharan, J. Phys. Chem. A, 2014, 118, 3663
35. I. V. Alabugin, M. Manoharan, J. Comput. Chem., 2007, 28, 373
36. L. J. Beckham, H. Adkins, J. Am. Chem. Soc., 1934, 56, 1119
37. T. Aoyama, S. Kubota, T. Takido, M. Kodomari, Chem. Lett., 2011, 40, 484
38. Y.-L. Wu, C.-P. Chuang, P.-Y. Lin, Tetrahedron, 2001, 57, 5543