References
- Lee, S.-H.; Kim, M.-J.; Bok, S. H.; Lee, H.; Kwon, B. -M. J. Org. Chem. 1998, 63, 7111. https://doi.org/10.1021/jo980919p
- Lee, S.-H.; Kang, H.-M.; Song,H.-C.; Lee, H.; Lee, U. C.; Son, K.-H.; Kim, S.-H.; Kwon, B.-M.Tetrahedron 2000, 56, 4711. https://doi.org/10.1016/S0040-4020(00)00394-X
- Lee, S.-H.; Kim, H.-K.; Seo,J.-M.; Kang, H.-M.; Kim, J.-H.; Son, K.-H.; Lee, H.; Kwon, B.-M.;Shin, J.; Seo, Y. J. Org. Chem. 2002, 67, 7670. https://doi.org/10.1021/jo020299z
- Lee, S.-H.; Lee, M.-Y.; Kang, H.-M.; Han, D. C.; Son, K.-H.; Yang, D. C.; Sung, N.-D.; Lee, C. W.; Kim, H. M.; Kwon, B.-M. Bioorg. Med. Chem. 2003, 11, 4545. https://doi.org/10.1016/j.bmc.2003.08.008
- Agrawal, A. G.; Somani, R. R. Mini-Rev. Med. Chem. 2009, 9, 638. https://doi.org/10.2174/138955709788452702
- Lee, H.-Y.; Sohn, J.-H.; Kim, H. Y.; Kwon, B.-M. Tetrahedron Lett. 2001, 42, 1695. https://doi.org/10.1016/S0040-4039(00)02324-8
- Sohn, J.-H. Bull. Korean Chem. Soc. 2009, 30, 2517. https://doi.org/10.5012/bkcs.2009.30.11.2517
- Jakupovic, J.; Chem, Z.-L.; Bohlmann, F. Phytochemistry1987, 26, 2777. https://doi.org/10.1016/S0031-9422(00)83589-X
- Bohlman, F.; Zdero, C. Phytochemistry 1978, 17, 1595. https://doi.org/10.1016/S0031-9422(00)94650-8
- Zhang, W.; Luo, S.; Fang, F.; Chen, Q.; Hu, H.; Jia,X.; Zhai, H. J. Am. Chem. Soc. 2005, 127, 18. https://doi.org/10.1021/ja0439219
- Wong, H.-F.;Brown, G. D. J. Nat. Prod. 2002, 65, 481. https://doi.org/10.1021/np0103113
- Tamao, K.; Kawachi, A.; Tanaka, Y.; Ohtani, H.; Ito, Y. Tetrahedron1996, 52, 5765. https://doi.org/10.1016/0040-4020(96)00212-8
- Fleming, I. Chem. Rev. 1997, 97, 2063. https://doi.org/10.1021/cr941074u
- Katritzky, A. R. Chem. Rev. 1989, 89, 827. https://doi.org/10.1021/cr00094a006
- Lefebvre, Y. Tetrahedron Lett. 1972, 13, 133. https://doi.org/10.1016/S0040-4039(01)84259-3
Cited by
- Synthetic Studies on Arglabin Diene; An Alleged Precursor to Arteminolides vol.33, pp.1, 2012, https://doi.org/10.5012/bkcs.2012.33.1.289
- ChemInform Abstract: Studies Toward Synthesis of Arteminolides: Intramolecular [5 + 2] Oxidopyrylium Ion Cycloaddition Reactions with Silicon Tether. vol.41, pp.48, 2010, https://doi.org/10.1002/chin.201048191
- Silicon-Tethered Intramolecular [5+2] Oxidopyrylium-Based Cycloaddition and Reductive Cleavage of Ether Bridge: Synthetic Studies Toward Arteminolides vol.35, pp.1, 2010, https://doi.org/10.5012/bkcs.2014.35.1.23
- Anodic Cyclizations, Seven‐Membered Rings, and the Choice of Radical Cation vs. Radical Pathways vol.37, pp.7, 2010, https://doi.org/10.1002/cjoc.201900132