참고문헌
- Knolker, H.-J.; Reddy, K. R. Chem. Rev. 2002, 102, 4303. https://doi.org/10.1021/cr020059j
- Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V. ComprehensiveHeterocyclic Chemistry II; Elsevier Science Ltd., 1996; Vol. 2, pp1-117.
- Kirsch, G. H. Current Organic Chemistry 2001, 5, 507. https://doi.org/10.2174/1385272013375409
- Pierre, A.; Atass, G.; Devissaguet, M.; Bisagni, E. Drugs Fut.1997, 22, 53 and references therein.
- Desarbrec, E.; Merour, J.-Y. Heterocycles 1995, 41, 1987. https://doi.org/10.3987/COM-95-7102
- Merour, J.-Y.; Joseph, B. Current Organic Chemistry 2001, 5, 471. https://doi.org/10.2174/1385272013375427
- Larock, R. C. J. Organomet. Chem. 1999, 576, 111. https://doi.org/10.1016/S0022-328X(98)01053-5
- Larock, R. C. Pure and Appl. Chem. 1999, 71, 1435. https://doi.org/10.1351/pac199971081435
- Li, J.J.; Gribble, G. W. Palladium in Heterocyclic Chemistry; Pergamon:2000; pp 143-146.
- Larock, R. C.; Yum, E. K. J. Am. Chem. Soc. 1991, 113, 6689. https://doi.org/10.1021/ja00017a059
- Larock, R. C.; Yum, E. K.; Reffik, D. J. Org. Chem. 1998, 63,7652. https://doi.org/10.1021/jo9803277
- Hong, K. B.; Lee, C. W.; Yum, E. K. Tetrahedron Lett.2004, 45, 693. https://doi.org/10.1016/j.tetlet.2003.11.075
- Roesch, K. R.; Larock, R. C. Org. Lett. 1999, 1, 1551. https://doi.org/10.1021/ol9901873
- Roesch, K. R.; Larock, R. C. J. Org. Chem. 2001, 66, 412. https://doi.org/10.1021/jo000997o
- Zhang, H.; Larock, R. C. Org. Lett. 2002, 4, 3035. https://doi.org/10.1021/ol026255u
- Zhang,H.; Larock, R. C. J. Org. Chem. 2003, 68, 5132. https://doi.org/10.1021/jo0343228
- Park, S. S.; Choi, J.-K.; Yum, E. K.; Ha, D.-C. TetrahedronLett. 1998, 39, 627. https://doi.org/10.1016/S0040-4039(97)10662-1
- Chi, S. M.; Choi, J.-K.; Yum, E. K.; Chi,D. Y. Tetrahedron Lett. 2000, 41, 919. https://doi.org/10.1016/S0040-4039(99)02190-5
- Lee, M. S.; Yum, E. K.Bull. Korean Chem. Soc. 2002, 23, 535. https://doi.org/10.5012/bkcs.2002.23.4.535
- Kang, S. K.; Park, S, S.; Kim, S. S.; Choi, J.-K.; Yum, E. K.Tetrahedron Lett. 1999, 40, 4379. https://doi.org/10.1016/S0040-4039(99)00753-4
- Yum, E. K.; Kang, S. S.;Kim, S. S.; Choi, J.-K.; Cheon, H. G. Bioorg. Med. Chem. Lett.1999, 9, 1819. https://doi.org/10.1016/S0960-894X(99)00291-7
- Gee, M. B.; Lee, W. J.; Yum, E. K. Bull. KoreanChem. Soc. 2003, 24, 1193. https://doi.org/10.5012/bkcs.2003.24.8.1193
- Lee, W. J.; Gee, M. B.; Yum, E. K.Heterocycles 2003, 60, 1821. https://doi.org/10.3987/COM-03-9798
- Kang, S. S.; Yum, E. K.; Sung, N.-D. Heterocycles 2003, 60,2727. https://doi.org/10.3987/COM-03-9895
- Williams, D. A.; Lemke, T. L. Foye's Principles of MedicinalChemistry, 5th ed; Lippincott Williams & Wilkins: 2002.
- Marsais, F.; Gogard, A.; Queguiner, G. J. Heterocycl. Chem. 1989,26, 1589. https://doi.org/10.1002/jhet.5570260615
- Queguiner, G. J. Heterocycl. Chem. 2000, 37, 615. https://doi.org/10.1002/jhet.5570370318
피인용 문헌
- Palladium-Catalyzed Synthesis of 2,3-Disubstituted 5-Azaindoles via Heteroannulation Reaction and of 2-Substituted 5-Azaindoles through Domino Sila-Sonogashira/5-Endo Cyclization vol.77, pp.11, 2012, https://doi.org/10.1021/jo300481s
- Synthesis of Tetracyclic 5-Azaindole Analogues by Palladium-Catalyzed Sequential Annulation. vol.36, pp.9, 2005, https://doi.org/10.1002/chin.200509139
- Organometallic methods for the synthesis and functionalization of azaindoles vol.36, pp.7, 2007, https://doi.org/10.1039/b607868k
- Metal‐Catalyzed Cross‐Coupling Reactions of Aminopyridines vol.2015, pp.33, 2004, https://doi.org/10.1002/ejoc.201500952
- Metal-Free Carbonyl-Assisted Regioselective Hydration of Alkynes: An Access to Dicarbonyls vol.21, pp.13, 2019, https://doi.org/10.1021/acs.orglett.9b01649