References
- Tafesh, A. M.; Weiguny, J. Chem. Rev. 1996, 96, 2035. https://doi.org/10.1021/cr950083f
- Spanu, P.; Ulgheri, F. Curr. Org. Chem. 2008, 12, 1071. https://doi.org/10.2174/138527208785740319
- Zakrzewski, J.; Krawczyk, M. Heteroatom Chem. 2006, 17, 393. https://doi.org/10.1002/hc.20228
- Klingstedt, F.; Arve, K.; Eranen, K.; Murzin, D. Y. Acc. Chem. Res. 2006, 39, 273. https://doi.org/10.1021/ar050185k
- Das, J.; Lin, J.; Moquin, R. V.; Shen, Z.; Spergel, S. H.; Wityak,J.; Doweyko, A. M.; DeFex, H. F.; Fang, Q.; Pang, S.; Pitt, S.; Shen,D. R.; Schieven, G. L.; Barrish, J. C. Bioorg. Med. Chem. Lett.2003, 13, 2145. https://doi.org/10.1016/S0960-894X(03)00380-9
- Kurihara, M.; Rouf, A. S. S.; Kansui, H.;Kagechika, H.; Okuda, H.; Miyata, N. Bioorg. Med. Chem. Lett.2004, 14, 4131. https://doi.org/10.1016/j.bmcl.2004.06.038
- Christianson, D. W. Acc. Chem. Res. 2005, 38, 191. https://doi.org/10.1021/ar040183k
- Doyle,A. J.; Jacobsen, E. N. Chem. Rev. 2007, 107, 5713. https://doi.org/10.1021/cr068373r
- Zhang, Z.;Schreiner, P. R. Chem. Soc. Rev. 2009, 38, 1187. https://doi.org/10.1039/b801793j
- Bell, T. W.; Hext, N. M. Chem. Soc. Rev. 2004, 33, 589.
- Amendola, V.; Esteban-Gómez, D.; Fabbrizzi, L.; Licchelli, M.Acc. Chem. Res. 2006, 39, 343. https://doi.org/10.1021/ar050195l
- Borovik, A. S. Acc. Chem. Res. 2005, 38, 54. https://doi.org/10.1021/ar030160q
- Petersen, U. In Methoden der Organischen Chemie: Houben-Weyl;E4; G. Thieme Verlag: New York, 1983; pp 334.
- Majer, P.; Randad, R. S. J. Org. Chem. 1994, 59, 1937. https://doi.org/10.1021/jo00086a061
- Barrett, A. G. M.; Betts, M. J.; Fenwick, A. J. Org. Chem.1985, 50, 169. https://doi.org/10.1021/jo00202a006
- Wang, Y.; Wheelhouse, R. T.; Zhao, L.; Langnel,D. A. F.; Stevens, M. F. G. J. Chem. Soc., Perkin Trans. 1 1998,1669.
- Basha, A. Tetrahedron Lett. 1988, 29, 2525. https://doi.org/10.1016/S0040-4039(00)86102-X
- Matsumura, Y.;Satoh, Y.; Onomura, O.; Maki, T. J. Org. Chem. 2000, 65, 1549. https://doi.org/10.1021/jo991076k
- Aguirre, I. de; Collot, J. Bull. Soc. Chim. Belg. 1989, 98, 19.
- Grupte, S. P.; Chaudhari, R. V. J. Catal. 1988, 114, 246. https://doi.org/10.1016/0021-9517(88)90028-0
- Shi, F.; Deng, Y.; SiMa, T.; Yang, H. Tetrahedron Lett. 2001, 42,2161. https://doi.org/10.1016/S0040-4039(01)00124-1
- Gabriele, B.; Salerno, G.; Mancuso, R.; Costa, M. J. Org. Chem. 2004, 69, 4741. https://doi.org/10.1021/jo0494634
- Mulla, S. A. R.; Rode, C. V.; Kelkar, A. A.; Gupte, S. P. J. Mol. Catal. A. Chem. 1997, 122, 103. https://doi.org/10.1016/S1381-1169(97)00023-X
- Bassoli, A.; Rindone, B.; Tollari, S.; Chioccara, F. J. Mol. Catal.1990, 60, 41. https://doi.org/10.1016/0304-5102(90)85065-P
- Dombek, B. D.; Angelici, R. J. J. Organomet. Chem. 1977, 134,203. https://doi.org/10.1016/S0022-328X(00)81420-5
- Sonoda, N.; Yasuhara, T.; Kondo, K.; Ikeda, T.; Tsutsumi, S. J. Am. Chem. Soc. 1971, 93, 6344. https://doi.org/10.1021/ja00752a099
- Yoshida, T.; Kambe, N.; Murai,S.; Sonoda, N. Tetrahedron Lett. 1986, 27, 2037. https://doi.org/10.1016/S0040-4039(00)84442-1
- Sonoda, N. Pure Appl. Chem. 1993, 65, 699. https://doi.org/10.1351/pac199365040699
- McCusker, J. E.; Main, A. D.; Johnson, K. S.; Grasso, C. A.;McElwee-White, L. J. Org. Chem. 2000, 65, 5216. https://doi.org/10.1021/jo000364+
- McCusker,J. E.; Qian, F.; McElwee-White, L. J. Mol. Catal. A-Chem. 2000,159, 11. https://doi.org/10.1016/S1381-1169(00)00164-3
- Han, H.; Bae, I.; Yoo, E. J.; Lee, J.; Do, Y.; Chang, S. Org. Lett. 2004, 6, 4109. https://doi.org/10.1021/ol0481784
- Bae, I.; Han, H.; Chang, S. J. Am. Chem. Soc. 2005, 127, 2038. https://doi.org/10.1021/ja0432968
- Cho. S. H.; Yoo, E. J.; Bae, I.; Chang.S. J. Am. Chem. Soc. 2005, 127, 16046. https://doi.org/10.1021/ja056399e
- Yoo. E. J.; Bae, I.; Cho,S. H.; Han, H.; Chang, S. Org. Lett. 2006, 8, 1347. https://doi.org/10.1021/ol060056j
- Chang, S.;Lee, M. J.; Jung, D. Y.; Yoo, E. J.; Cho, S. H.; Han, S. K. J. Am. Chem. Soc. 2006, 128, 12366. https://doi.org/10.1021/ja064788i
- Han, H.; Park, S. B.; Kim, S. K.;Chang. S. J. Org. Chem. 2008, 73, 2862. https://doi.org/10.1021/jo800134j
- Brewster, J. H.; Eliel, E. L. In Organic Reactions; Adams, R., Ed.; John Wiley and Sons: New York, 1953; Vol. VII, pp 142.
- Olofoson, R. A.; Schur, R. C.; Bunes, L.; Pepe, J. P. Tetrahedron Lett. 1977, 18, 1567. https://doi.org/10.1016/S0040-4039(01)93104-1
- Cooley, J. H.; Evain, E. J. Synthesis 1989, 1.
- Ko, S.; Na, Y.; Chang, S. J. Am. Chem. Soc.2002, 124, 750. https://doi.org/10.1021/ja017076v
- Ko, S.; Lee, C.; Choi, M.-G.; Na, Y.; Chang, S.J. Org. Chem. 2003, 68, 1607. https://doi.org/10.1021/jo026591o
- Ko, S.; Han, H.; Chang, S. Org. Lett. 2003, 5, 2687. https://doi.org/10.1021/ol034862r
- Na, Y.; Ko, S.; Hwang, L. K.; Chang, S.Tetrahedron Lett. 2003, 44, 4475. https://doi.org/10.1016/S0040-4039(03)01016-5
- Ko, S.; Kang, B.; Chang, S.Angew. Chem., Int. Ed. 2005, 44, 455. https://doi.org/10.1002/anie.200462006
- Park, E. J.; Lee, J. M.;Han, H.; Chang, S. Org. Lett. 2006, 8, 4355. https://doi.org/10.1021/ol061753e
- Trost, B. M. In Comprehensive Oganic Synthesis; Pergamon:Oxford, 1991; pp 795.
- Abdul Hai, S. M.; Perveen, S.; Khan, R. A.; Khan, K. M.; Afza,N. Nat. Prod. Res. 2003, 17, 351. https://doi.org/10.1080/1057563031000072613
- Aranha, R. M.; Bowser, A.M.; Madalengoitia, J. S. Org. Lett. 2009, 11, 575. https://doi.org/10.1021/ol802577z
- Okazaki, R.; Tokitoh, N. J. Chem. Soc., Chem. Commun. 1984,192.
- Monkovic, I.; Wong, H.; Bachand, C. Synthesis 1985, 770.
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