References
- Noyori, R.; Kitamura, M. Angew. Chem. Int. Ed.Engl. 1991, 30, 49. https://doi.org/10.1002/anie.199100491
- Soai, K.; Niwa, S. Chem. Rev. 1992, 92,833. https://doi.org/10.1021/cr00013a004
- Sola, L.; Reddy, K. S.; Vidal-Ferran, A.; Moyano, A.; Perica,M. A.; Riera, A.; Alvarez-Larena, A.; Piniella, J. J. Org. Chem.1998, 63, 7078. https://doi.org/10.1021/jo981336i
- Cho, B. T.; Chun, Y. S. Tetrahedron: Asymmetry1998, 9, 1489. https://doi.org/10.1016/S0957-4166(98)00143-8
- Tanner, D.; Korno, T.; Guijarro, D.; Andersson,P. G. Tetrahedron 1998, 54, 14213. https://doi.org/10.1016/S0040-4020(98)00875-8
- Bolm, C.; Muniz, K.;Hildebrand, J. P. Org. Lett. 1999, 1, 491. https://doi.org/10.1021/ol990683r
- Xu, Q.; Pan, X.;Chan, A.; Yang, T. Tetrahedron Lett. 2001, 42, 6171. https://doi.org/10.1016/S0040-4039(01)01236-9
- Rosini, C.; Franzini, L.; Pini, D.; Salvadori, P. Tetrahedron:Asymmetry 1990, 1, 587. https://doi.org/10.1016/0957-4166(90)80007-L
- Schmit, B.; Seebach, D. Angew.Chem. Int. Ed. Engl. 1991, 30, 1321. https://doi.org/10.1002/anie.199113211
- Weber, B.; Seebach, D.Tetrahedron 1994, 50, 7473. https://doi.org/10.1016/S0040-4020(01)90475-2
- Huang, W.-S.; Hu, Q.-S.; Pu, L. J.Org. Chem. 1999, 64, 7940. https://doi.org/10.1021/jo990992v
- Soai, K.; Niwa, S.; Yamada, Y.; Inoue, H. Tetrahedron Lett.1987, 28, 4841. https://doi.org/10.1016/S0040-4039(00)96639-5
- Rosini, C.; Franzini, L.; Iuliano, A.; Pini, D.;Salvadori, P. Tetrahedron Asymmetry 1991, 2, 363. https://doi.org/10.1016/S0957-4166(00)82120-5
- Conti, S.;Falorni, M.; Giacomelli, G.; Soccolini, F. Tetrahedron 1992, 48,8993. https://doi.org/10.1016/S0040-4020(01)81997-9
- Yoshioka, M.; Kawakita, T.; Ohno, M. Tetrahedron Lett. 1989,30, 1657. https://doi.org/10.1016/S0040-4039(00)99546-7
- Katsuji, I.; Kimula, Y.; Okamura, H.; Katsuki, T.Synlett 1992, 573.
- Kang, J.; Kim, J. W.; Lee, J. W.; Kim, D. S.;Kim, J. L. Bull. Korean Chem. Soc. 1996, 17, 1135.
- Vettel, S.;Lutz, C.; Diefenbach, A.; Harderlein, G.; Hammerschmidt, S.;Kuhling, K.; Mofid, M.-R.; Zimmermann, T.; Knochel, P. Tetrahedron:Asymmetry 1997, 8, 779. https://doi.org/10.1016/S0957-4166(97)00036-0
- Ramon, D. J.; Yus, M. Tetrahedron:Asymmetry 1997, 8, 2479. https://doi.org/10.1016/S0957-4166(97)00272-3
- Jin, M.-J.; Kim, S.-H.;Jung, J.-A.; Lee, H.-Y. Bull. Korean Chem. Soc. 2000, 21, 33.
- Kim, S.-H.; Ahn, S.-J.; Chung, S.-T.; Jin, M.-J. J. Ind. & Eng.Chem. 1997, 3, 37.
- Calmes, M.; Escale, F.; Paolini, F. Tetrahedron: Asymmetry 1997,8, 3691. https://doi.org/10.1016/S0957-4166(97)00480-1
- Brunner, H.; Becker, R.; Riepl, G. Organometallics 1984, 3, 1354. https://doi.org/10.1021/om00087a006
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