An improved procedure for the epoxidation of methyl cinnamate derivatives and production of acid sensitive epoxides

Synthetic Communications

Volumn 26, Issue 11, 1996, Pages 2235-2239

  Moyna, Guillermo ^a   Williams, Howard J ^a   Scott, A I ^a  

^a TEXAS A AND M UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EPOXIDE;

ARTICLE; DRUG SYNTHESIS; EPOXIDATION; TECHNIQUE;

EID: 0030004122     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003584     Document Type: Article

References (11)

1. For a review on routes to the Taxol® side chain, see: Nicolau, K. C., Dai, W.-M. and Gary, R. K. Angew. Chem., 1994, 33, 15.
2. Concerning structural studies of Taxol®: a) Williams, H. J. et al, and Krauss, N. E. et al. Tetrahedron, 1993, 49, 6545. b) Williams, H. J. et al, and Krauss, N. E. et al. Can. J. Chem., 1994, 72, 252.
3. Concerning structural studies of Taxol®: a) Williams, H. J. et al, and Krauss, N. E. et al. Tetrahedron, 1993, 49, 6545. b) Williams, H. J. et al, and Krauss, N. E. et al. Can. J. Chem., 1994, 72, 252.
4. K. Ishikawa, H. C. Charles, G. W. Griffin. Tetrahedron Lett., 1977, 427.
5. W. K. Anderson, T. Veysoglu. J. Org. Chem., 1973, 38, 2267.
6. Fieser & Fieser. Reagents for Organic Synthesis. Wiley & Sons, New York, 1967, 135-139.
7. C. A. Kingsbury, G. Max. J. Org. Chem., 1978, 43, 3131.
8. Organic Reactions I. Whiley & Sons, New York, 1963, 210-265.
9. a) G. P. Schiemenz, J. Thobe. Chem. Ber., 1966, 99, 2663-2668.
10. b) H. J. Kosterman, R. Z. Muggli. J. Am. Chem. Soc., 1959, 81, 2188-2191.
11. c) P. L. Southwick, R. T. Crouch, J. Am. Chem. Soc., 1953, 75, 3413-3417.