References
- (a) Pellati, F.; Calo, S.; Benvenuti, S.; Adinolfi, B.; Nieri, P.; Melegari, M. Phytochemistry 2006, 67, 1359–1364. (b) Resch, M.; Heilman, J.; Steigel, A.; Bauer, R. Planta Med. 2001, 67, 437–442. (c) Choi, Y. E.; Ahn, H.; Ryu, J.-H. Biol. Pharm. Bull. 2000, 23, 884–886. (d) Zgoda, J. R.; Freyer, A. J.; Killmer, L. B.; Porter, J. R. J. Nat. Prod. 2001, 64, 1348–1349. (e) Hudson, J. G.; Graham, E. A.; Chan, G.; Finlayson, A. J.; Towers, G. H. N. Planta Med. 1986, 453–457. (f) Shi Shun, A. L. K.; Tykwinski, R. R. Angew. Chem., Int. Ed. 2006, 45, 1034–1057. doi: 10.1016/j.phytochem.2006.05.006
- Watanabe, K.; Tsuda, Y.; Yamane, Y.; Takahashi, H.; Iguchi, K.; Naoki, H.; Fujita, T.; Van Soest, R. W. M. Tetrahedron Lett. 2000, 41, 9271–9276. doi: 10.1016/S0040-4039(00)01692-0
- (a) Katano, M.; Yamamoto, H.; Matsunaga, H.; Mori, M.; Takata, K.; Nakamura, M. Gan to Kagakuyoho 1990, 17, 1045–1049. (b) Matsunaga, H.; Saita, T.; Naguo, F.; Mori, M.; Katano, M. Cancer Chemother. Pharmacol. 1995, 35, 291–296.
- Hu, D.-B.; Li, W.-X.; Zhao, Z.-Z.; Feng, T.; Yin, R.-H.; Li, Z.-H.; Liu, J.-K.; Zhu, H.-J. Tetrahedron Lett. 2014, 55, 6530–6533. doi: 10.1016/j.tetlet.2014.09.132
- (a) Yadav, J. S.; Chander, M. C.; Joshi, B. V. Tetrahedron Lett. 1988, 29, 2737–2740. (b) Yadav, J. S.; Chander, M. C.; Rao, C. S. Tetrahedron Lett. 1989, 30, 5455–5458. (c) Yadav, J. S.; Rajagopal, D. Tetrahedron Lett. 1990, 31, 5077–5080. (d) Yadav, J. S.; Chander, M. C.; Reddy, K. K. Tetrahedron Lett. 1992, 33, 135–138. (e) Yadav, J. S.; Deshpande, P. K.; Sharma, G. V. M. Tetrahedron 1990, 46, 7033–7046. (f) Yadav, J. S.; Deshpande, P. K.; Sharma, G. V. M. Tetrahedron Lett. 1990, 31, 4495–4496. (g) Yadav, J. S.; Chander, M. C. Tetrahedron Lett. 1990, 31, 4349–4350. (h) Yadav, J. S.; Mishra, R. K. Tetrahedron Lett. 2002, 43, 1739–1741. (i) Yadav, J. S.; Maiti, A. Tetrahedron 2002, 58, 4955–4961. (j) Yadav, J. S.; Kumaraswamy, B.; Sathish, R. A.; Srihari, P.; Janakiram, R. V.; Shasi, V. K. J. Org. Chem. 2011, 76, 2568–2576. (k) Kanikarapu, S. Marumudi K.; Kunwar, A. C.; Yadav, J. S.; Mohapatra, D. K. Org. Lett. 2017, 19, 4167−4170. (l) Rangaraju, S. K.; Gonela, U. M.; Kavita, A.; Yadav, J. S.; Mohapatra, D. K. Eur. J. Org. Chem. 2018, 32, 4376−4380. doi: 10.1016/0040-4039(88)85274-2
- Mohapatra, D. K.; Umamaheshwar, G.; Rao, R. N.; Rao, T. S.; Kumar, S. R.; Yadav, J. S. Org. Lett. 2015, 17, 979–981. doi: 10.1021/acs.orglett.5b00138
- Nishikawa, T.; Shibuya, S.; Hosokawa, S.; Isobe, M. Synlett 1994, 1994, 485–486. doi: 10.1055/s-1994-22897
- Cadiot, P.; Chodkiewicz, W. In Chemistry of Acetylenes; Viehe, H. G., Ed.; Marcel Dekker: New York, 1969, pp 597–647.
- Sonogashira, K. In Handbook of Organopalladium Chemistryfor Organic Synthesis; Negishi, E., Ed.; Wiley-Interscience: New York, 2002; Vol. 1, pp 493–529. The formation of homocoupling products during the cross-coupling reaction has been observed earlier. For reviews, see (b) Negishi, E.; Anastasia, L. Chem. Rev. 2003, 103, 1979–2017. (c) Siemsen, P.; Livingston, R. C.; Diederich, F. Angew. Chem., Int. Ed. 2000, 39, 2632–2657.