91024-63-4Relevant articles and documents
The Regiochemistry of the Radical Addition of N-Chloroamides to Enol Ethers
Caron, Gilles,Lessard, Jean
, p. 8039 - 8058 (2007/10/02)
The orientation of the radical addition of N-chloroamides (ZCONHCl) to enol ethers was studied as a function of Z and the enol ether structure and compared with the orientation of radical addition of thioacetic acid and the orientation of typical electrop
PHOTO-SENSITIZED OXYGENATION OF MONOCYCLIC 1H-1,3-DIAZEPINES
Kurita, Jyoji,Kojima, Hirokazu,Tsuchiya, Takashi
, p. 721 - 724 (2007/10/02)
The sensitized photooxygenation of monocyclic 1H-1,3-diazepines (1a-c) affords fragment products (2) to(7), which may be derived from the corresponding 4,7-endoperoxides (8) or the 4,5-dioxetanes (9) initially formed.The other possible dioxides and their decomposition products are not detected.