Effect of cyclodextrin complexation on photo-Fries rearrangement of naphthyl esters
β Scribed by Habeeb Shayira Banu; Kasi Pitchumani; Chockalingam Srinivasan
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 491 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Photolysis of [~-cydodextrin inclusion complexes of 1-and 2-naphthyi esters (acetates and benzeat~) in aqueous metfium, results in ~ to give one isomer of acylnaphthol in excess, whereas the solid state irra~ation of the Β’yclodextrin ~ yields soleftivety otlg isomer. In addition, formation of cleavage product is totally ~, This remadralble scle~vity ia attrilmt~ to specific mocks of the complexation of the esters into the [~,CD cavity.
π SIMILAR VOLUMES
1-Naphthyl phenyl acylates upon irradiation in solution yield eight products via b-cleavage process. However, excitation of these molecules as included in g-cyclodextrin results in a single product (>95%). This medium dependent product selectivity is attributed to conformational and translational re