References
- Puentes, C. O.; Kouznetsov, V. J. Heterocyclic Chem.2002, 39, 595-614. https://doi.org/10.1002/jhet.5570390401
- Lou, S.; Moquist, P. N.; Schaus, S. E. J. Am. Chem. Soc. 2007, 129, 15398-15404. https://doi.org/10.1021/ja075204v
- Albano, V. G.; Gualandi,A.; Monari, M.; Savoia, D. J. Org. Chem. 2008, 73, 8376-8381. https://doi.org/10.1021/jo8014598
- Katritzky, A. R.; Ignatchenko, A. V.; Lang, H. J. Org. Chem. 1995,60, 4002-4005. https://doi.org/10.1021/jo00118a015
- Del Valle, J. R.; Goodman, M. J. Org. Chem.2004, 69, 8946-8948. https://doi.org/10.1021/jo0485738
- White, J. D.; Hansen, J. D. J. Org. Chem.2005, 70, 1963-1977. https://doi.org/10.1021/jo0486387
- Nicolaou, K. C.; Mitchell, H. J.; van Delft,F. L.; Rubsam, F.; Rodriguez, R. M. Angew. Chem. Int. Ed. 1998,37, 1871-1874. https://doi.org/10.1002/(SICI)1521-3773(19980803)37:13/14<1871::AID-ANIE1871>3.0.CO;2-1
- Robl, J. A.; Cimarusti, M. P.; Simpkins, L. M.;Brown, B.; Ryono, D. E.; Bird, J. E.; Asaad, M. M.; Schaeffer, T. R.;Trippodo, N. C. J. Med. Chem. 1996, 39, 494-502. https://doi.org/10.1021/jm950677a
- Vilaivan, T.;Winotapan, C.; Banphavichit, V.; Shinada, T.; Ohfune, Y. J. Org. Chem. 2005, 70, 3464-3471. https://doi.org/10.1021/jo0477244
- Rueping, M.; Antonchick, A. P. Angew. Chem. Int. Ed. 2008, 47, 10090-10093. https://doi.org/10.1002/anie.200803610
- Singh, P.; Kaur, P.;Luxami, V.; Kaur, S.; Kumar, S. Bioorg. Med. Chem. 2007, 15,2386-2395. https://doi.org/10.1016/j.bmc.2007.01.018
- Kumar, S.; Kaur, P. Tetrahedron Lett. 2004, 45,3413-3416. https://doi.org/10.1016/j.tetlet.2004.03.022
- Fiorelli, C.; Savoia, D. J. Org. Chem. 2007, 72,6022-6028. https://doi.org/10.1021/jo0703000
- Suvire, F. D.; Sortino, M.; Kouznetsov, V.V.; Vargas M, L. Y.; Zacchino, S. A.; Cruz, U. M.; Enriz, R. D.Bioorg. Med. Chem. 2006, 14, 1851-1862. https://doi.org/10.1016/j.bmc.2005.10.036
- Janjic, J. M.; Mu,Y.; Kendall, C.; Stephenson, C. R. J.; Balachandran, R.; Raccor,B. S.; Lu, Y.; Zhu, G.; Xie, W.; Wipf, P.; Day, B. W. Bioorg. Med. Chem. 2005, 13, 157-164. https://doi.org/10.1016/j.bmc.2004.09.048
- Doherty, A. M.; Sircar, I.; Kornberg,B. E.; Quin, J., III.; Winters, T.; Kaltenbronn, J. S.; Taylor, M. D.;Batley, B. L.; Rapundalo, S. R.; Ryan, M. J.; Painchaud, C. A. J. Med. Chem. 1992, 35, 2-14. https://doi.org/10.1021/jm00079a001
- Kim, S. H.; Lee, H. S.; Kim, K. H.;Kim, J. N. Tetrahedron Lett. 2009, 50, 1696-1698. https://doi.org/10.1016/j.tetlet.2009.01.149
- Kim, S.H.; Kim, S. H.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2009, 50,5744-5747. https://doi.org/10.1016/j.tetlet.2009.07.140
- Kim, S. H.; Lee, H. S.; Kim, K. H.; Kim, J. N. Tetrahedron Lett. 2009, 50, 6476-6479. https://doi.org/10.1016/j.tetlet.2009.09.013
- Kim, S. H.; Kim, S. H.; Kim,K. H.; Kim, J. N. Tetrahedron Lett. 2010, 51, 860-862. https://doi.org/10.1016/j.tetlet.2009.12.034
- Kim, S.H.; Kim, S. H.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2010, 51,2774-2777. https://doi.org/10.1016/j.tetlet.2010.03.076
- Du,Z.; Li, Y.; Wang, F.; Zhou, W.; Wang, J.-X. Tetrahedron Lett. 2010,51, 1745-1747. https://doi.org/10.1016/j.tetlet.2010.01.092
- Lombardo, M.; Pasi, F.; Trombini, C. Eur. J. Org. Chem. 2006, 3061-3063.
- Kim, S. H.; Kim, Y. M.; Kim,J. N. Bull. Korean Chem. Soc. 2010, 31, 2351-2356. https://doi.org/10.5012/bkcs.2010.31.8.2351
- Takamura, M.;Funabashi, K.; Kanai, M.; Shibasaki, M. J. Am. Chem. Soc. 2000,122, 6327-6328. https://doi.org/10.1021/ja0010352
- Takamura, M.; Funabashi, K.; Kanai, M.; Shibasaki,M. J. Am. Chem. Soc. 2001, 123, 6801-6808. https://doi.org/10.1021/ja010654n
- Yadav, J.S.; Reddy, B. V. S.; Srinivas, M.; Sathaiah, K. Tetrahedron Lett.2005, 46, 3489-3492. https://doi.org/10.1016/j.tetlet.2005.03.127
- Popp, F. D.; Kant, J. Heterocycles 1985,23, 2193-2195. https://doi.org/10.3987/R-1985-09-2193
- Lizarraga, E.; Zabaleta, C.; Palop, J. A. Thermochim. Acta 2005, 427, 171-174. https://doi.org/10.1016/j.tca.2004.09.008
- Gibson, H. W.; Guilani, B. J. Org. Chem. 1990, 55, 4226-4229. https://doi.org/10.1021/jo00300a056
- Elliott, I. W., Jr. J. Am. Chem. Soc. 1955, 77, 4408-4409.
- Wolf, A. P.; McEwen, W. E.; Glazier,R. H. J. Am. Chem. Soc. 1956, 78, 861-868. https://doi.org/10.1021/ja01585a043
- Popp, F. D.; Blount,W.; Melvin, P. J. Org. Chem. 1961, 26, 4930-4932. https://doi.org/10.1021/jo01070a036
- Auge, J.; Lubin-Germain, N.; Uziel, J. Synthesis 2007, 1739-1764.
- Li, C.-J.; Chan, T.-H. Tetrahedron 1999, 55, 11149-11176. https://doi.org/10.1016/S0040-4020(99)00641-9
- Kim, S. H.; Lee, H. S.; Kim, K. H.; Kim, S. H.; Kim, J. N. Tetrahedron2010, 66, 7065-7076 https://doi.org/10.1016/j.tet.2010.05.103
- Fuchs, C.; Bender,C.; Ziemer, B.; Liebscher, J. J. Heterocyclic Chem. 2008, 45, 1651-1658. https://doi.org/10.1002/jhet.5570450615
- Davey, D.; Erhardt, P. W.; Lumma, W. C., Jr.; Wiggins,J.; Sullivan, M.; Pang, D.; Cantor, E. J. Med. Chem. 1987, 30,1337-1342. https://doi.org/10.1021/jm00391a012
- Iwao, M.; Kuraishi, T. J. Heterocyclic Chem. 1979,16, 689-698. https://doi.org/10.1002/jhet.5570160416
- Kant, J. J. Heterocyclic Chem. 1990, 27, 2129-2132. https://doi.org/10.1002/jhet.5570270751
Cited by
- ChemInform Abstract: Regioselective Introduction of Homoallylic Amine Moiety to Quinolines: Preparation of Reissert Compound Followed by In-Mediated Allylation of Nitrile. vol.42, pp.17, 2011, https://doi.org/10.1002/chin.201117155
- Regioselective synthesis of functionalized dihydroquinolines via organocatalytic allylic alkylation vol.32, pp.4, 2016, https://doi.org/10.1007/s40242-016-5481-3