References
- Lee, M. J.; Lee, K. Y.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 477 https://doi.org/10.5012/bkcs.2005.26.3.477
- Hong, W. P.; Lim, H. N.; Park, H. W.; Lee, K.-J. Bull. Korean Chem. Soc. 2005, 26, 655 https://doi.org/10.5012/bkcs.2005.26.4.655
- Gaul, C.; Njardarson, J. T.; Danishefsky, S. J. J. Am. Chem. Soc. 2003, 125, 6042 https://doi.org/10.1021/ja0349103
- Gaul, C.; Njardarson, J. T.; Shan, D.; Dorn, D. C.; Wu, K.-D.; Tong, W. P.; Huang, X.-Y.; Moore, M. A. S.; Danishefsky, S. J. J. Am. Chem. Soc. 2004, 126, 11326 https://doi.org/10.1021/ja048779q
- Powell, R. G.; Smith, C. R., Jr.; Weisleder, D. J. Am. Chem. Soc. 1983, 105, 3739 https://doi.org/10.1021/ja00349a081
- Suarez, A. I.; Blanco, Z.; Monache, F. D.; Compagnone, R. S.; Arvelo, F. Nat. Prod. Res. 2004, 18, 421 https://doi.org/10.1080/14786410310001622004
- Nakae, K.; Yoshimoto, Y.; Sawa, T.; Homma, Y.; Hamada, M.; Takeuchi, T.; Imoto, M. J. Antibiot. 2000, 53, 1130 https://doi.org/10.7164/antibiotics.53.1130
- Urakawa, A.; Otani, T.; Yoshida, K.-I.; Nakayama, M.; Suzukake-Tsuchiya, K.; Hori, M. J. Antibiot. 1993, 46, 1827 https://doi.org/10.7164/antibiotics.46.1827
- Wanner, M. J.; Koomen, G. J. Tetrahedron Lett. 1990, 31, 907 https://doi.org/10.1016/S0040-4039(00)94660-4
- Wanner, M. J.; Koomen, G. J. Synthesis 1988, 325
- Wanner, M. J.; Koomen, G. J. Tetrahedron Lett. 1992, 33, 1513 https://doi.org/10.1016/S0040-4039(00)91662-9
- Basavaiah, D.; Kumaragurubaran, N.; Sharada, D. S. Tetrahedron Lett. 2001, 42, 85 https://doi.org/10.1016/S0040-4039(00)01886-4
- Basavaiah, D.; Kumaragurubaran, N.; Sharada, D. S.; Reddy, R. M. Tetrahedron 2001, 57, 8167 https://doi.org/10.1016/S0040-4020(01)00786-4
- Basavaiah, D.; Sharada, D. S.; Kumaragurubaran, N.; Reddy, R. M. J. Org. Chem. 2002, 67, 7135 https://doi.org/10.1021/jo0257952
- Grigg, R.; Dorrity, M. J.; Heaney, F.; Malone, J. F.; Rajviroongit, S.; Sridharan, V.; Surendrakumar, S. Tetrahedron 1991, 47, 8297 https://doi.org/10.1016/S0040-4020(01)91022-1
- Grigg, R.; Malone, J. F.; Dorrity, M. R. J.; Heaney, F.; Rajviroongit, S.; Sridharan, V.; Surendrakumar, S. Tetrahedron Lett. 1988, 29, 4323 https://doi.org/10.1016/S0040-4039(00)80487-6
- Luxenburger, A. Tetrahedron 2003, 59, 3297 https://doi.org/10.1016/S0040-4020(03)00412-5
- Moorthy, J. N.; Singhal, N. J. Org. Chem. 2005, 70, 1926 https://doi.org/10.1021/jo048240a
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