References
- Organic Reactions v.51 Ciganek, E.
- Tetrahedron v.44 Drewes, S. E.;Roos, G. H. P.
- Tetrahedron v.52 Basavaiah, D.;Rao, P. D.;Hyma, R. S.
- Tetrahedron Lett. v.41 Kim, H. S.;Kim, T. Y.;Lee, K. Y.;Chung, Y. M.;Lee, H. J.;Kim, J. N.
- Tetrahedron Lett. v.39 Lee, H. J.;Seong, M. R.;Kim, J. N.
- Tetrahedron Lett. v.40 Lee. H. J.;Kim, H. S.;Kim, J. N.
- Org. Lett. v.2 Kim, J. N.;Lee, K. Y.;Kim, H. S.;Kim. T. Y.
- J. Chem. Soc. Chem. Commun. Familoni, O. B.;Kaye, P. T.;Klaas, P. J.
- J. Chem. Soc. Perkin Trans. 1 Bide, M.L.;Kaye, P. T.
- J. Chem. Soc. Perkin Trans. 1 Bode, M. L.';Kaye, P. T.
- Nat. prod. Rep. v.14 Micheal, J. P.
- Comprehensive Heterocyclic Chemistry II v.5 Balasubramanian, M.;Keay, J. G.;Katrizky, A. R.;Ress, C. W.;Scriven, E. F. V. (Ed.)
- Comprehensive Heterocyclic Chemistry II v.5 Jones, G.;Katrizky, A. R.;Ress, C. W.;Scriven, E. F. V. (Eds.)
- Tetrahedron Lett. v.41 Ranu, B. C.;Hajra, A.;Jana, U.
- Tetrahedron Lett. v.40 Cho, C. S.;Oh, B. H.;Shim, S. C.
- Synlett Cacchi, S.;Fabrizi, G.;Marinelli, F.
- Org. Lett. v.1 Suginome, M.;Fukuda, T.;Ito, Y.
- J. Org. Chem. v.63 Katritzky, A. R.;Arend, M.
- For the photolysis experiments a Raynot photochemical reactor (model RPR-2080, the Southern N. E. Ultraviolet Co.) was used. The built-in monochromatic UV light sources (RUL-250 nm UV lamp) was positioned approximately 17cm from the reaction quartz tube
- Org. Lett. v.1 Woodrell, C. D.;Kehayova, P. D.;Jain, A.
- J. Org. Chem. v.64 Pirrung, M. C.;Lee, Y. R.;Park, K.;Springer, J. B.
- J. Org. Chem. v.59 Pirrung, M. C.;Shuey, S. W.
- J. Am. Chem. Soc. v.110 Walker, J. W.;Reid, G. P.;McGray, J. A.;Trentham, D. R.
- J. Am. Chem. Soc. v.106 Givens, R. D.;Matuszewski, B.
- J. Org. Chem. v.39 Amit, B.;Zehavi, U.;patchorik, A.
- J. Am. Chem. Soc. v.114 Givens, R. S.;Athey, P. S.;Kueper, L. W.III;Matuszewski, B.;Xue, J.-y.
- J. Am. Chem. Soc. v.115 Givens, R. S.;Athey, P.S.;Matuszewski, B.;Kueper, L. W.;Xue, J.-y.;Fister, T.
- Synthesis v.1 Pillai, V. N. R.
- Chem. Rev. v.93 Givens, R. S.;Kueper, L. W. III.
- Chem. Ber. v.98 Bredereck, H.;Effenberger, F.;Botsch, H.;Rehn, H.
Cited by
- Isatin derivatives are reactive electrophilic components for the Baylis–Hillman reaction vol.43, pp.11, 2001, https://doi.org/10.1016/s0040-4039(02)00160-0
- Facile Synthesis of 3-Substituted 2(1H)-Quinolinones from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes vol.23, pp.7, 2001, https://doi.org/10.5012/bkcs.2002.23.7.939
- A Double Carbon-Carbon Bond Activation of 8-Quinolinyl Cyclopropyl Ketone by Chlorobis(ethylene)rhodium(I) Dimer vol.24, pp.8, 2001, https://doi.org/10.5012/bkcs.2003.24.8.1059
- Synthesis of 3-Substituted Quinolines via Transition-Metal-Catalyzed Reductive Cyclization of o-Nitro Baylis−Hillman Acetates vol.68, pp.16, 2001, https://doi.org/10.1021/jo034447c
- Copper‐Catalyzed Aerobic Oxidative Carbocyclization– Ketonization Cascade: Selective Synthesis of Quinolinones vol.355, pp.11, 2013, https://doi.org/10.1002/adsc.201300160