198402-07-2Relevant academic research and scientific papers
The synthesis of 4-aminocarbonylmethoxy trinems
Bertani, Barbara,Di Fabio, Romano,Ghiron, Chiara,Perboni, Alcide,Rossi, Tino,Thomas, Russell J.,Zarantonello, Paola
, p. 15011 - 15028 (2007/10/03)
The synthesis of 4-aminocarbonylmethoxy trinems was accomplished through Lewis acid catalysed opening of an epoxide intermediate with allyl glycolate, followed by deallylation, activation of the free acid via the 2-pyridyl thiolester and reaction with a series of trimethylsilylamines. An alternative route involving a rhodium-catalysed diazoacetate insertion was also successfully exploited.
