1 Mori, J., 54 : 391-3911, 2006
2 Ishizuka, N., 45 : 2041-2041, 2002
3 Nicolaou, K. C., 112 : 9939-9939, 2000
4 Sundén, H., 13 : 574-574, 2007
5 Li, H., 507 : 2007
6 Hardouin, C., 44 : 435-435, 2003
7 Lee, M. H., 5630 : 2008
8 Choi, E. T., 64 : 1515-1515, 2008
9 Kim, Y., 48 : 2833-2833, 2007
10 "The selectivity factor (s = kS / kR) was estimated using the equation, s = ln[(1-C)(1-ees)]/ln[(1-C)(1 + ees)], where ees is the enantiomeric excess of unconverted β-hydroxy esters and the conversion (C) determined by 1H NMR of reaction mixture using internal standard. For the reactions of 11-16 the conversion (C) was calculated using the equation: C = 100 × ees / (ees + eep), where eep is the enantiomeric excess of eliminated products 17-22"
1 Mori, J., 54 : 391-3911, 2006
2 Ishizuka, N., 45 : 2041-2041, 2002
3 Nicolaou, K. C., 112 : 9939-9939, 2000
4 Sundén, H., 13 : 574-574, 2007
5 Li, H., 507 : 2007
6 Hardouin, C., 44 : 435-435, 2003
7 Lee, M. H., 5630 : 2008
8 Choi, E. T., 64 : 1515-1515, 2008
9 Kim, Y., 48 : 2833-2833, 2007
10 "The selectivity factor (s = kS / kR) was estimated using the equation, s = ln[(1-C)(1-ees)]/ln[(1-C)(1 + ees)], where ees is the enantiomeric excess of unconverted β-hydroxy esters and the conversion (C) determined by 1H NMR of reaction mixture using internal standard. For the reactions of 11-16 the conversion (C) was calculated using the equation: C = 100 × ees / (ees + eep), where eep is the enantiomeric excess of eliminated products 17-22"
11 Yong Sun Park, "Stereoselective Syntheses of 3-Substituted Flavene Derivatives and Asymmetric Dehydration via Kinetic Resolution" 대한화학회 29 (29): 1299-1300, 2008
12 Eui Ta Choi, "Asymmetric Dehydration of β-Styryl-β-hydroxy Esters and Applicationto the Synthesis of a Neoflavonoid" 대한화학회 29 (29): 859-862, 2008