Steroids of unnatural configuration. Part X. A quantitative study of the epoxidation of lumisterol and its esters

Autor: K. D. Bingham, J. Wicha, G. D. Meakins
Rok vydání: 1969
Předmět:
Zdroj: Journal of the Chemical Society C: Organic. :510
ISSN: 0022-4952
DOI: 10.1039/j39690000510
Popis: Oxidation of lumisterol with perbenzoic and peroxylauric acids, and of lumisteryl acetate and lumisteryl 3,5-di-nitrobenzoate with peroxylauric acid gives 5β,6β-epoxides in high yields. The second-order rate constants (l. mole–1 sec.–1) are respectively 12·6, 3·35, 2·58 × 10–2, and 1·76 × 10–2: bonding in the transition state is thought to accelerate the reactions of lumisterol. Ring-opening of the 3β-hydroxy-5β,6β-epoxide with benzoic acid to the 3β,5β-dihydroxy-6β-benzoate is much slower (k 5·72 × 10–5).
Databáze: OpenAIRE