39608-52-1Relevant articles and documents
-
Hirao,I. et al.
, p. 2775 - 2779 (1976)
-
Einfuehrung von Sauerstoff-Funktionen in die α-Stellung von β-Diketonen, 5. Acyloxylierung von 3-prim.-Amino-2-cyclohexen-1-onen
Schank, Kurt,Adler, Manfred
, p. 2019 - 2028 (2007/10/02)
The enaminone 1 reacts with diacyl peroxides 2 to yield monoacyloxylation products 4 and (acylamino)cyclohexadienolones 6 which may be regarded as reaction products of an acyl rearrangement of the non-isolable bis-acyloxylation products 5.Catalytic hydrogenation of benzyl esters 4e and 6e obtained by the described way leads immediately to the amino reductone 8.