Highly enantioselective rearrangement of quaternary carbon-containing meso-epoxides to allylic alcohols

Tetrahedron Asymmetry

Volumn 7, Issue 2, 1996, Pages 407-408

  Hodgson, David M ^a   Gibbs, Andrew R ^a  

^a UNIVERSITY OF READING   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENONE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030063386     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00019-5     Document Type: Article

References (10)

1. Cox, P. J.; Simpkins, N. S. Tetrahedron: Asymmetry 1991, 2, 1-26.
2. For a tertiary alcohol prepared using this strategy see: Asami, M.; Ishizaki, T.; Inoue, S. Tetrahedron Lett. 1995, 36, 1893-1894.
3. Hodgson, D. M.; Witherington, J.; Moloney, B. A. J. Chem. Soc., Perkin Trans. 1 1994, 3373-3378.
4. Fuji, K. Chem. Rev. 1993, 93, 2037-2066.
5. Crandall, J. K.; Apparu, M. Org. React. (N. Y.) 1983, 29, 345-443.
6. Deprés, J.-P.; Greene, A. E. J. Org. Chem. 1984, 49, 928-931. Paulsen, H.; Maaß, U. Chem. Ber. 1981, 114, 346-358.
7. Deprés, J.-P.; Greene, A. E. J. Org. Chem. 1984, 49, 928-931. Paulsen, H.; Maaß, U. Chem. Ber. 1981, 114, 346-358.
8. Isolated total yields of chromatographically homogeneous, spectroscopically pure products are reported.
9. Mash, E. A.; Fryling, J. A. J. Org. Chem. 1987, 52, 3000-3003.
10. Full details will be reported at a later date.