10.1002/ejoc.201701250
European Journal of Organic Chemistry
FULL PAPER
Chem. 2013, 6656–6665; (h) J. Park, E. Park, A. Kim,
631; b) L. Mahendar, G. Satyanarayana, J. Org.
Chem. 2014, 79, 2059–2074; c) L. Mahendar, G.
Satyanarayana, J. Org. Chem. 2015, 80, 7089–7098;
(d) D. R. Kumar, G. Satyanarayana, Org. Lett. 2015,
17, 5894–5897; (e) J. Krishna, A. G. K. Reddy, G.
Satyanarayana, Adv. Synth. Catal. 2015, 357, 3597–
3610; (f) L. Mahendar, G. Satyanarayana, J. Org.
Chem. 2016, 81, 76857691; (g) A. G. K. Reddy, G.
Satyanarayana, J. Org. Chem. 2016, 81, 12212-
12222; (h) K. Ramesh, G. Satyanarayana, J. Org.
Chem. 2017, 82, 4254-4264; (i) B. Suchand, G.
Satyanarayana, Eur. J. Org. Chem. 2017, 26, 3886–
3895.
Y. Lee, K. W. Chi, J. H. Kwak, Y. H. Jung, I. S. Kim,
Org. Lett. 2011, 13, 4390–4393; (i) H. Wang, L. N.
Guo, X. H. Duan, Org. Lett. 2012, 14, 4358–4361; (j)
W. Zhou, H. Li, L. Wang, Org. Lett. 2012, 14, 4594–
4597; (k) F. Xiong, C. Qian, D. Lin, W. Zeng, X. Lu,
Org. Lett. 2013, 15, 5444–5447.
4. Y. Kobayashi, T. Harayama, Org. Lett. 2009, 11,
1603-1606.
5. (a) J. M. Kraus, H. B. Tatipaka, S. A. McGuffin, N. K.
Chennamaneni, M. Karimi, J. Arif, C. L. M. J.
Verlinde, F. S. Buckner, M. H. Gelb, J. Med. Chem.
2010, 53, 3887-3898; (b) P. Cheng, Q. Zhang, Y.-B.
Ma, Z.-Y. Jiang, X.-M. Zhang, F.-X. Zhang, J.-J.
Chen, Bioorg. Med. Chem. Lett. 2008, 18, 3787-3789;
(c) C. Peifer, R. Urich, V. Schattel, M. Abadleh, M.
Rꢀttig, O. Kohlbacher, S. Laufer, S. Bioorg. Med.
Chem. Lett. 2008, 18, 1431-1435.
6. (a) T. Murayama, M. Shibuya, Y. Yamamoto, Y. J.
Org. Chem. 2016, 81, 11940-11949; (b) R. Zeng, G.
Dong, J. Am. Chem. Soc. 2015, 137, 1408-1411; (c)
K. K. Park, J. J. Lee Tetrahedron 2004, 60, 2993–
2999; (d) X. Chen, X. Cui, Y. Wu, Org. Lett. 2016, 18,
2411-2414; (e) K. Michalak, J. Wicha, Tetrahedron
Lett. 2017, 58, 1917-1920; (f) C. Qi, T. Guo, W.
Xiong, L. Wang, H. Jiang, ChemistrySelect 2017, 2,
4691-4695; (g) T. N. Glasnov, W. Stadlbauer, C. O.
Kappe, J. Org. Chem. 2005, 70, 3864-3870. (h) A. C.
Tadd, A. Matsuno, M. R. Fielding, M. C. Willis, Org.
Lett. 2009, 11, 583-586.
7. a) X. Li, X. Li, N. Jiao, J. Am. Chem. Soc. 2015, 137,
9246-9249; (b) D. V. Kadnikov, R. C. Larock, J. Org.
Chem. 2004, 69, 6772-6780; (c) P. J. Manley, M. T.
Bilodeau, W. Point, V. Pennsyl, Org. Lett. 2004, 6,
2433-2435; (d) T. Vacala, L. P. Bejcek, C. G.
Williams, A. C. Williamson, P. A. Vadola, J. Org.
Chem. 2017, 82, 2558-2569; (e) C. Jia, D. Piao, T.
Kitamura, Y. Fujiwara, J. Org. Chem. 2000, 65, 7516-
7522; (f) K. Inamoto, T. Saito, K. Hiroya, T. Doi, J.
Org. Chem. 2010, 75, 3900-3903; (g) H. Alper, J.
Guson, F. Zeng, N. Alwis, Org. Lett. 2013, 15, 1998-
2001; (h) S. Song Sun, H. Wei-Ming, N. Gu, J.
Cheng, Chem. - A Eur. J. 2016, 22, 18729-18732; (i)
Z. Zhang, L. L. Liao, S. S. Yan, L. Wang, Y. Q. He, J.
H. Ye, J. Li, Y. G. Zhi, D. G. Yu, Angew. Chemie - Int.
Ed. 2016, 55, 7068-7072; (j) R. Manikandan, M.
Jeganmohan, Org. Lett. 2014, 16, 3568-3571; (k) R.
Kancherla, T. Naveen, D. Maiti, Chem. - A Eur. J.
2015, 21, 8360-8364; (l) Y. Deng, W. Gong, J. He, J.
Q. Yu, Angew. Chemie - Int. Ed. 2014, 53, 6692-
6695; (m) T. Iwai, T. Fujihara, J. Terao, Y. Tsuji, J.
Am. Chem. Soc. 2010, 132, 9602-9603; (n) J. Wu, S.
Xiang, J. Zeng, M. Leow, X. W. Liu, Org. Lett. 2015,
17, 222-225.
9. B. Suchand, G. Satyanarayana, J. Org. Chem. 2016,
81, 6409-6423.
10. B. Suchand, G. Satyanarayana, J. Org. Chem. 2017,
82, 372-381.
11. Y. Wu, B. Li, F. Mao, X. Li, Y. F. Kwong, Org. Lett.
2011, 13, 3258-3261.
12. a) F. Szabó, B. Pethő, Z. Gonda, Z. Novák, RSC Adv.
2013, 3, 4903–4908. b) D. Evans, M. E. Cracknell, J.
C. Saunders, C. E. Smith, W. R. Williamson, W.
Dawson, W. J. Sweatman, J. Med. Chem. 1987, 30,
1321–1327. c) L. Meng, J. Su, Z. Zha, L. Zhang, Z.
Zhang, Z. Wang, Chem. - A Eur. J. 2013, 19, 5542–
5545. d) Z. D. Yang, Z. W. Song, J. Ren, M. J. Yang,
S. Li, Phytochem. Anal. 2011, 22, 509–515. e) B.
Zhao, X. Lu, Org. Lett. 2006, 8, 5987–5990. f) Y. Ji,
X. Yang, W. Mao, Appl. Organomet. Chem. 2014, 28,
678–680.
13. a) J. Chen, L. Ye, W. Su, Org. Biomol. Chem. 2014,
12, 8204–8211. b) M. Aidene, F. Belkessam, J. F.
Soulé, H. Doucet, ChemCatChem 2016, 8, 1583–
1590. c) E. Barile, S. K. De, Y. Feng, V. Chen, L.
Yang, Z. Ronai, M. Pellecchia, Chem. Biol. Drug Des.
2013, 82, 520–533.
14. (a) R. Labaudinihre, W. Hendel, B. Terlain, F. Cavy,
O. Marquis, N. Dereu, J. Med. Chem. 1992, 35,
4306–4314. b) D. S. Ryabukhin, A. V. Vasilyev,
Tetrahedron Lett. 2015, 56, 2200–2202. c) Y. N.
Huang, Y. L. Li, J. Li, J. Deng, J. Org. Chem. 2016,
81, 4645–4653. d) J. M. Kraus, C. L. M. J. Verlinde,
M. Karimi, G. I. Lepesheva, H. Gelb, F. S. Buckner, J.
Med. Chem. 2009, 52, 1639–1647.
15. (a) F. Szabo, D. Simko, Z. Novak, RSC Adv. 2014, 4,
3883-3886. (b) C. Li, L. Lei Wang, P. Li, W. Zhou, W.
Chem. - A Eur. J. 2011, 11, 10208-10212.
16. A. Pialat, B. Liegault, M. Taillefer, Org. Lett. 2013, 15,
1764-1767.
8. (a) L. Mahendar, J. Krishna, A. G. K. Reddy, B. V.
Ramulu, G. Satyanarayana, Org. Lett. 2012, 14, 628–
This article is protected by copyright. All rights reserved.