52909-80-5Relevant articles and documents
Photorearrangement of N-alkanoyl β-enaminones. Application to the synthesis of α-amino-β,γ-unsaturated acid derivatives
Amougay,Letsch,Pete,Piva
, p. 2405 - 2420 (2007/10/03)
The irradiation of N-alkanoyll-β-enaminones lead to the formation of spiranic β-lactams which undergo C-N bond cleavage during chromatography on alumina giving cycloalkenones functionalized at position 3. This new rearrangement has been applied to the synthesis of α-amino-β,γ-unsaturated amides in one step and gives convenient yields.
AMINO-DERIVATIVES OF 4-METHOXY-7,8-DIHYDRO-1,3-DIAZAPHENOTHIAZINE AND THEIR NEUROTROPIC ACTIVITY
Nemeryuk, M. P.,Tolokontseva, L. A.,Yadrovskaya, V. A.,Polezhaeva, A. I.,Petrova, G. A.,et al.
, p. 459 - 462 (2007/10/02)
-