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Effect of cyclodextrin complexation on photo-Fries rearrangement of naphthyl esters

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


Cyclodextrin-mediated regioselective pho
✍ Smriti Koodanjeri; Ajit R Pradhan; Lakshmi S Kaanumalle; V Ramamurthy πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 French βš– 143 KB

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