Browse > Article
http://dx.doi.org/10.5012/bkcs.2012.33.7.2415

Diastereoselective Reduction of Chiral 2-(1-Alkenoyl)- and 2-(1-Alkynoyl)-1,3-Oxathiane 3-Oxides Derived from (1R)-(+)-Camphor  

Ko, Kwang-Youn (Department of Chemistry, Ajou University)
Yun, Ho-Seop (Division of Energy Systems Research, Ajou University)
Publication Information
Keywords
Diastereoselective reduction; Camphor; Chelate model;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
Times Cited By Web Of Science : 0  (Related Records In Web of Science)
연도 인용수 순위
1 Mengel, A.; Reiser, O. Chem. Rev. 1999, 99, 1191.   DOI
2 Roberstson, J.; Unsworth, W. P.; Lamont, S. G. Tetrahedron 2010, 66, 2363.   DOI
3 Colombo, L.; Di Giacomo, M.; Brusotti, G.; Milano, E. Tetrahedron Lett. 1995, 36, 2863.   DOI
4 Harder, T.; Lohl, T.; Bolte, M.; Wagner, K.; Hoppe, D. Tetrahedron Lett. 1994, 35, 7365.   DOI
5 Eliel, E. L.; He, X.-C. J. Org. Chem. 1990, 55, 2114.   DOI
6 Fukuzawa, S.; Miura, M.; Matsuzawa, H. Tetrahedron Lett. 2001, 42, 4167.   DOI
7 Uiterweerd, P. G. H.; van der Sluis, M.; Kaptein, B.; de Lange, B.; Kellogg, R. M.; Broxtermanb, Q. B. Tetrahedron: Asymmetry 2003, 14, 3479.   DOI
8 Ko, K.-Y.; Kim, K.-I. Bull. Korean Chem. Soc. 1998, 19, 911.
9 Bailey, W. F.; Reed, D. P.; Clark, D. R.; Kapur, G. N. Org. Lett. 2001, 3, 1865.   DOI
10 Ko, K.-Y.; Park, J.-Y. Bull. Korean Chem. Soc. 2002, 23, 665.   DOI
11 Solladie, G. In Advanced Asymmetric Synthesis; Stephenson, G. R., Ed.; Blackie: 1996.
12 Page, P. C. B.; Prodger, J. C. Synlett. 1990, 460.
13 Ko, K.-Y.; Kim, K.-I. Bull. Korean Chem. Soc. 1998, 19, 379.
14 Herscovici, J.; Antonakis, K. J. Chem. Soc., Chem. Commun. 1980, 561.
15 The enantiomeric excess of 6a was found to be ca. 96% by the proton NMR study of its 2-phenyl-1,3-dioxolanes doped with Eu(hfc)3. See: Eliel, E. L.; Ko, K.-Y. Tetrahedron Lett. 1983, 24, 3547.   DOI
16 Cossy, J. Synthesis 1987, 1113.
17 Takano, S.; Iwabuchi, Y.; Ogasawara, K. Synlett. 1991, 548.
18 Chun, J.; Byun, H.-S.; Bittman, R. J. Org. Chem. 2003, 68, 348.   DOI
19 Lebel, H.; Marcoux, J.-F.; Molinaro, C.; Charette, A. B. Chem. Rev. 2003, 103, 977.   DOI
20 Ratier, M.; Castaing, M.; Godet, J. Y.; Pereyre, M. J. Chem. Res., Synop. 1978, 179.
21 Charette, A. B.; Lebel, H. J. Org. Chem. 1995, 60, 2966.   DOI
22 Mori, A.; Arai, I.; Yamamoto, H. Tetrahedron 1986, 42, 6447.   DOI
23 Chacon-García, L.; Lagunas-Rivera, S.; Perez-Estrada, S.; Vargas- Diaz, M. E.; Joseph-Nathan, P.; Tamariz, J.; Gerardo Zepeda, L. Tetrahedron Lett. 2004, 45, 2141.   DOI
24 Ko, K.-Y.; Park, J.-Y. Tetrahedron Lett. 1997, 38, 407.   DOI
25 Ko, K.-Y.; Yun, H. Heterocycles 2010, 81, 2351.   DOI
26 Ko, K.-Y.; Frazee, W. J.; Eliel, E. L. Tetrahedron 1984, 40, 1333.   DOI