RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2018; 50(17): 3460-3466
DOI: 10.1055/s-0037-1610070
DOI: 10.1055/s-0037-1610070
paper
Radical Addition/Cyclization Cascade: An Efficient Approach to Nitro-Containing Quinoline-2,4(1H,3H)-diones
We acknowledge the financial support from the National Natural Science Foundation of China (No. 21662021), the Applied Basic Research Foundation of Yunnan Province (2016DC032), and the Analysis and Testing Foundation of Kunming University of Science and Technology (2016T20130138, 20150725).Weitere Informationen
Publikationsverlauf
Received: 28. März 2018
Accepted after revision: 28. April 2018
Publikationsdatum:
18. Juni 2018 (online)
Abstract
A radical addition/cyclization cascade of o-cyanoarylacrylamides with magnesium nitrate hexahydrate is developed. This reaction exhibits good functional group tolerance and wide substrate scope, provides a highly efficient and practical access to nitro-containing quinoline-2,4(1H,3H)-diones.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1610069.
- Supporting Information
-
References
- 1a Kitamura S. Hashizume K. Iida T. Miyashitsa E. Shirata K. Kase H. J. Antibiot. 1986; 39: 1160
- 1b Seong CM. Park WK. Park CM. Kong JY. Park NS. Bioorg. Med. Chem. Lett. 2008; 18: 738
- 1c McCormick JL. McKee TC. Cardellina JH. Boyd MR. J. Nat. Prod. 1996; 59: 469
- 1d Ahmed N. Brahmbhatt KG. Sabde S. Mitra D. Singh IP. Bhutani KK. Bioorg. Med. Chem. 2010; 18: 2872
- 1e Han S. Zhang F.-F. Qian H.-Y. Chen L.-L. Pu J.-B. Xie X. Chen J.-Z. J. Med. Chem. 2015; 58: 5751
- 1f Liu Y.-X. Zhao H.-P. Wang Z.-W. Li Y.-H. Song H.-B. Riches H. Beattie D. Gu Y.-C. Wang Q.-M. Mol. Divers. 2013; 17: 701
- 2a Chauncey MA. Grundon MF. Synthesis 1990; 1005
- 2b Klásek A. Mrkvička V. Pevec A. Košmrlj J. J. Org. Chem. 2004; 69: 5646
- 2c Jung EJ. Park BH. Lee YR. Green Chem. 2010; 12: 2003
- 3a Hamama WS. El-Din A. Hassanien E. Zoorob HH. Synth. Commun. 2014; 44: 1833
- 3b Kumabe R. Nishino H. Tetrahedron Lett. 2004; 45: 703
- 3c Kafka S. Proisl K. Kasparkova V. Urankar D. Kimmel R. Kosmrlj J. Tetrahedron 2013; 69: 10826
- 3d Zografos AL. Mitsos CA. Igglessi-Markopoulou O. Org. Lett. 1999; 1: 1953
- 3e Antolak SA. Yao Z.-K. Richoux GM. Slebodnick C. Carlier PR. Org. Lett. 2014; 16: 5204
- 4a Feuer H. Nielson AT. Nitro Compounds: Recent Advances in Synthesis and Chemistry. VCH; Weinheim: 1990
- 4b Ono N. The Nitro Group in Organic Synthesis . Wiley-VCH; New York: 2001
- 4c Barrett AG. M. Graboski GG. Chem. Rev. 1986; 86: 751
- 5a Shechter H. Conrad F. Daulton AL. Kaplan RB. J. Am. Chem. Soc. 1952; 74: 3052
- 5b Jovel I. Prateeptongkum S. Jackstell R. Vogl N. Weckbecker C. Beller M. Adv. Synth. Catal. 2008; 350: 2493
- 5c Olah GA. Ramaiah P. Rao CB. Graham S. Golam R. Trivedi NJ. Olah JA. J. Am. Chem. Soc. 1993; 115: 7246
- 5d Kornbblum N. Powers JW. J. Org. Chem. 1957; 22: 455
- 5e Emmons WD. J. Am. Chem. Soc. 1957; 79: 5528
- 5f Suzuki H. Nonoyama N. Chem. Commun. 1996; 1783
- 5g Deng G.-B. Zhang J.-L. Liu Y.-L. Liu B. Yang X.-H. Li J.-H. Chem. Commun. 2015; 51: 1886
- 5h Zhou Y. Tang Z. Song Q. Chem. Commun. 2017; 53: 8972
- 6a Maity S. Manna S. Rana S. Naveen T. Mallick A. Maiti D. J. Am. Chem. Soc. 2013; 135: 3355
- 6b Li Y.-M. Wei X.-H. Li X.-A. Yang S.-D. Chem. Commun. 2013; 49: 11701
- 6c Xue C. Fu C.-L. Ma S.-M. Chem. Commun. 2014; 50: 15333
- 6d Shen T. Yuan Y.-Z. Jiao N. Chem. Commun. 2014; 50: 554
- 6e Liu Y. Zhang J.-L. Song R.-J. Qian P.-C. Li J.-H. Angew. Chem. Int. Ed. 2014; 53: 9017
- 6f Yan H. Rong G. Liu D. Zheng Y. Chen J. Mao J. Org. Lett. 2014; 16: 6306
- 6g Hao X.-H. Gao P. Song X.-R. Qiu Y.-F. Jin D.-P. Liu X.-Y. Liang Y.-M. Chem. Commun. 2015; 51: 6839
- 6h Li X. Zhuang S. Fang X. Liu P. Sun P. Org. Biomol. Chem. 2017; 15: 1821
- 7a Clegg W. Davies RP. Dunbar L. Feeder N. Liddle ST. Mulvey RE. Snaith R. Wheatley AE. H. Chem. Commun. 1999; 1401
- 7b Malamas MS. Erdei J. Gunawan I. Barnes K. Johnson M. Hui Y. Turner J. Hu Y. Wagner E. Fan K. Olland A. Bard J. Robichaud AJ. J. Med. Chem. 2009; 52: 6314
- 7c Jie S. Zhang S. Sun W.-H. Eur. J. Inorg. Chem. 2007; 5584
- 8a Zhou C. Larock RC. J. Am. Chem. Soc. 2004; 126: 2302
- 8b Zhao B. Lu X. Org. Lett. 2006; 8: 5987
- 8c Miura T. Nakazawa H. Murakami M. Chem. Commun. 2005; 2855
- 8d Lindh J. Sjoberg PJ. R. Larhed M. Angew. Chem. Int. Ed. 2010; 49: 7733
- 8e Ma Y. You J. Song F. Chem.–Eur. J. 2013; 19: 1189
- 8f Tsui GC. Glenadel Q. Lau C. Lautens M. Org. Lett. 2011; 13: 208
- 8g Xia G. Han X. Lu X. Org. Lett. 2014; 16: 2058
- 9a Curran DP. In Comprehensive Organic Synthesis . Vol. IV. Trost BM. Flemming I. Pergamon Press; Oxford: 1991
- 9b Kim S. Adv. Synth. Catal. 2004; 346: 19
- 9c Beckwith AL. J. Raner KD. J. Org. Chem. 1992; 57: 4954
- 10a Forrester AR. Gill M. Thomson RH. J. Chem. Soc., Perkin Trans. 1 1974; 621
- 10b Kraus GA. Sy JO. J. Org. Chem. 1989; 54: 77
- 10c Snider BB. Buckman BO. J. Org. Chem. 1992; 57: 322
- 10d Montevecchi PC. Navacchia ML. Spagnolo P. J. Org. Chem. 1997; 62: 5846
- 10e Streuff J. Feurer M. Bichovski P. Frey G. Gellrich U. Angew. Chem. Int. Ed. 2012; 51: 8661
- 10f Zhao WX. Montgomery J. Angew. Chem. Int. Ed. 2015; 54: 12683
- 11a Fu H. Wang S.-S. Li Y.-M. Adv. Synth. Catal. 2016; 358: 3616
- 11b Wang S.-S. Fu H. Shen Y. Sun M. Li Y.-M. J. Org. Chem. 2016; 81: 2920
- 11c Wang S.-S. Fu H. Wang G. Sun M. Li Y.-M. RSC Adv. 2016; 6: 52391
- 11d Li Y.-M. Wang S.-S. Yu F.-C. Shen Y. Chang K.-J. Org. Biomol. Chem. 2015; 13: 5376
- 11e Wang S. Huang X. Wang Q. Ge Z. Wang X. Li R. RSC Adv. 2016; 6: 11754
- 12 Taniguchi T. Fujii T. Ishibashi H. J. Org. Chem. 2010; 75: 8126