Please use this identifier to cite or link to this item:
|Title:||Facile ketone sensitized photochemical ring opening of isoxazolidines to <i>β</i>-enaminocarbonyl compounds|
Ishar, Mohan Paul S
|Abstract:||Isoxazolidines, which are otherwise transparent (Pyrex-filter) to UV light, undergo both inter- and intramolecular ketone sensitized photocleavage to furnish <i style="">β</i>-enaminocarbonyl compounds. A series of experiments on variedly substituted isoxazolidines under different sets of irradiation conditions have been conducted to delineate the mechanistic details, in particular, the photosensitization by carbonyl moiety.|
|Appears in Collections:||IJC-B Vol.49B(02) [February 2010]|
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.