The regiochemistry of the radical addition of N-chloroamides to enol ethers
作者:Gilles Caron、Jean Lessard
DOI:10.1016/s0040-4020(01)88026-1
日期:1993.9
The orientation of the radical addition of N-chloroamides (ZCONHCl) to enolethers was studied as a function of Z and the enolether structure and compared with the orientation of radical addition of thioacetic acid and the orientation of typical electrophilicadditions.
Studies on diazepines. XXIV Reactions of monocyclic 1H-1,3-diazepines. 2 Photo-sensitized oxygenation.
作者:JYOJI KURITA、HIROKAZU KOJIMA、TAKASHI TSUCHIYA
DOI:10.1248/cpb.34.4871
日期:——
The photo-sensitized oxygenation of monocyclic 1H-1, 3-diazepines (6) gave several fragment products (7-12). 3-Pyrrolin-2-one derivatives (7 and 8) and ethyl aminoformates (9 and 10) are assumed to originate from the initially formed 4, 7-endoperoxides (13), and vinylaminoformates (11 and 12) from the 4, 5-dioxetanes (14).