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. Author manuscript; available in PMC: 2010 May 4.
Published in final edited form as: Chemistry. 2009 Dec 7;15(47):12978–12992. doi: 10.1002/chem.200902172

Table 14.

Resolution of 3-substituted cyclic allylic alcohols.

graphic file with name nihms194467u13.jpg
entry alcohol, major enantiomer conditions[a] time conv.[b] alcohol ee[c] s
1 graphic file with name nihms194467t31.jpg A 4 h 53% 99% 83
2 B 1 h 53% 98% 63
3 D 6 h 55% 94% 26
4 graphic file with name nihms194467t32.jpg A 4 h 56% 99% 50
5 B 1 h 56% 99% 51
6 C 9 h 51% 95% 83
7 graphic file with name nihms194467t33.jpg A 8 h 73% 98% 8.6
8 B 1 h 61% 85% 9.0
9 C 10 h 78% 99% 7.5
10 graphic file with name nihms194467t34.jpg R = Me
R = Bn
B 8 h 65% 99% 15
11 C 27 h 58% 94% 19
12 D 43 h 64% 97% 13
13 C 72 h 61% 91% 11
[a–c]

See Table 10 footnotes.