849937-09-3Relevant academic research and scientific papers
Unusual lability of α-silyloxy β-amino carboxylic acid derivatives
Greco, Michael N.,Zhong, H. Marlon,Maryanoff, Bruce E.
, p. 4959 - 4962 (1998)
Saponification and mild acidification of α-silyloxy homo-arginine derivative 2c revealed an unusual lability of the silyl protecting group. A systematic study of related substrates indicates that hydrogen bonding between the α-amino hydrogen and the carbo
Synthesis of functionalised azecine and azonine derivatives via an enolate assisted aza Claisen rearrangement
Bremner, John B.,Perkins, David F.
, p. 2659 - 2665 (2007/10/03)
This paper describes the synthesis of functionalised azecine and azonine derivatives incorporating the adrenaline motif. In a key step, an enolate assisted aza Claisen rearrangement was employed to interconvert from 6- and 5-membered heterocycles to their corresponding 10- and 9-membered lactams.
