References
- Quinoa, E.; Kakao, Y.; Crews, P. J. Org. Chem. 1988, 53, 3642-3644. https://doi.org/10.1021/jo00250a052
- Corley, D. G.; Herb, R.; Moore, R. E.; Scheuer, P. J.; Paul, V. J. J.Org. Chem. 1988, 53, 3644-3646. https://doi.org/10.1021/jo00250a053
- Jefford, C. W.; Bernardinelli, G.; Tanaka, J.; Higa, T. TetrahedronLett. 1996, 37, 159-162. https://doi.org/10.1016/0040-4039(95)02113-2
- Tanaka, J.; Higa, T.; Bernardinelli, G.;Jefford, C. W. Chem. Lett. 1996, 25, 255-256.
- Pryor, D. E.; O'Brate, A.; Bilcer, G.; Díaz, J. F.; Wang, Y.; Wang,Y.; Kabaki, M.; Jung, M. K.; Andreu, J. M.; Ghosh, A. K.;Giannakakou, P.; Hamel, E. Biochemistry 2002, 41, 9109-9115. https://doi.org/10.1021/bi020211b
- Williams, D. R.; Mi, L.; Mullins, R. J.; Stites, R. E. TetrahedronLett. 2002, 43, 4841-4844. https://doi.org/10.1016/S0040-4039(02)00907-3
- Crimmins, M. T.; Stanton, M. G.; Allwein, S. P. J. Am. Chem. Soc.2002, 124, 5958-5959. https://doi.org/10.1021/ja026269v
- Mulzer, J.; Hanbauer, M. Tetrahedron Lett. 2002, 43, 3381-3383. https://doi.org/10.1016/S0040-4039(02)00472-0
- Mulzer, J.; Ohler, E. Angew. Chem., Int. Ed. 2001, 40,3842-3846. https://doi.org/10.1002/1521-3773(20011015)40:20<3842::AID-ANIE3842>3.0.CO;2-R
- Enev, V. S.; Kaehlig, H.; Mulzer, J. J. Am. Chem.Soc. 2001, 123, 10764-10765. https://doi.org/10.1021/ja016752q
- Wender, P. A.; Hegde, S. G.; Hubbard, R. D.; Zhang, L. J. Am.Chem. Soc. 2002, 124, 4956-4957. https://doi.org/10.1021/ja0258428
- Ghosh, A. K.; Wang, Y.; Kim, J. T. J. Org. Chem. 2001, 66, 8973-8982. https://doi.org/10.1021/jo010854h
- Paterson, I.; De Savi, C.; Tudge, M. Org. Lett. 2001, 3, 3149-3152. https://doi.org/10.1021/ol010150u
- Lee, H. W.; Jeong, C.-S.; Yoon, S. H.; Lee, I.-Y. C. Bull.Korean Chem. Soc. 2001, 22, 791-792.
- Lee, H. W.; Yoon, S.H.; Lee, I.-Y. C.; Chung, B. Y. Bull. Korean Chem. Soc. 2001, 22,1179-1180.
- Vasil’ev, A. A.; Engman, L.; Serebryakov, E. P. J. Chem. Soc.,Perkin Trans. 1 2000, 2211-2216.
Cited by
- Cyclopropanol intermediates in the synthesis of the C5–C14 fragment of laulimalides vol.52, pp.3, 2016, https://doi.org/10.1134/S1070428016030118
- Synthesis of the C3—C12 Fragment of Laulimalide vol.35, pp.17, 2004, https://doi.org/10.1002/chin.200417219
- Synthesis of Dihydropyran Subunit of (+)-Sorangicin A Using RCM Reaction vol.29, pp.9, 2003, https://doi.org/10.5012/bkcs.2008.29.9.1661
- Metal-Mediated Diastereoselective Allylation Reaction of Chiral α,β-Epoxy Aldehyde. Part 2 vol.29, pp.9, 2003, https://doi.org/10.5012/bkcs.2008.29.9.1663