Photochemical addition of alkenes and alcohols to sodium phthalimide
作者:R.Suau Suarez、R.García Segura
DOI:10.1016/0040-4039(88)85338-3
日期:1988.1
The results of the photochemical reaction between sodium phthalimide and alkenes (1-hexene and cyclohexene) or alcohols (methanol and -butanol) are described.
The investigation of the photochemistry of phthalimide anion has uncovered its exceptional reactivity with hydrogen donors such as alcohols, toluene, ethers and amines, Photoreactions can be conducted to high conversions and photoadducts are formed in high yield and with predictable regioselectivity. Exploratory studies have revealed that SET from the excited phthalimide anion to phthalimide is a thermodinamically favourable step that produces the electrophilic phthalimidyl radical and is the key step of the process. (C) 2002 Elsevier Science Ltd. All rights reserved.
SATO, YASUHIKO;NAKAI, HIDEO;WADA, MASAO;OGIWARA, HIROSHI;MIZOGUCHI, TOMIS+, CHEM. AND PHARM. BULL., 1982, 30, N 5, 1639-1645