참고문헌
- Reatequi, R. F.; Gloer, J. B.; Campbell, J.; Shearer, C. A. J. Nat. Prod. 2005, 68, 701-705. https://doi.org/10.1021/np050035i
- Clarke, P. A.; Santos, S. Eur. J. Org. Chem. 2006, 2045-2053.
- Yadav, J. S.; Lakshmi, P. N.; Harshavardhan, S. J.; Subba Reddy,B. V. Synlett 2007, 1945-1947.
- Sharma, G. V. M.; Damera, K. Tetrahedron: Asymmetry 2008, 19,2092-2095. https://doi.org/10.1016/j.tetasy.2008.08.016
- Lee, D.-M.; Lee, H.; Kang, H.-Y. Bull. Korean Chem. Soc.2008, 29, 535-536. https://doi.org/10.5012/bkcs.2008.29.3.535
- Lee, D.-M.; Kang, H.-Y. Bull. Korean Chem. Soc. 2008, 29, 1671-1678. https://doi.org/10.5012/bkcs.2008.29.9.1671
- Lee, D.-M.; Kang, H.-Y. Bull. Korean Chem. Soc. 2009, 30, 1929-1930. https://doi.org/10.5012/bkcs.2009.30.9.1929
- Broggini, G.; Molteni, G.; Pilati, T. Tetrahedron: Asymmetry2000, 11, 1975-1983. https://doi.org/10.1016/S0957-4166(00)00132-4
- Schmidt, B.; Biernat, A. Chem. Eur. J.2008, 14, 6135-6141. https://doi.org/10.1002/chem.200800567
- Cai, Y.; Ling, C.-C.; Bundle, D. R. J. Org. Chem. 2009, 74, 580-589. https://doi.org/10.1021/jo801927k
피인용 문헌
- Stereoselective Total Synthesis of Ophiocerin C through Two Different Approaches vol.97, pp.11, 2014, https://doi.org/10.1002/hlca.201400086
- Recent applications in natural product synthesis of dihydrofuran and -pyran formation by ring-closing alkene metathesis vol.14, pp.25, 2016, https://doi.org/10.1039/C6OB00593D
- ChemInform Abstract: Synthesis of Ophiocerins from Non-Carbohydrate Sources. vol.41, pp.32, 2010, https://doi.org/10.1002/chin.201032196
- The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2010 vol.256, pp.13, 2010, https://doi.org/10.1016/j.ccr.2012.02.015
- Synthesis of Ophiocerins A, B and C, Botryolide E, Decarestrictine O, Stagonolide C and 9‐epi‐Stagonolide C Employing Chiral Hexane‐1,2,3,5‐tetraol Derivatives as Building Bloc vol.2016, pp.27, 2016, https://doi.org/10.1002/ejoc.201600625