1609691-79-3Relevant academic research and scientific papers
Silyl imine electrophiles in enantioselective catalysis: A rosetta stone for peptide homologation, enabling diverse N-protected aryl glycines from aldehydes in three steps
Makley, Dawn M.,Johnston, Jeffrey N.
supporting information, p. 3146 - 3149 (2014/06/23)
We report that N-(trimethylsilyl)imines serve in the Bis(AMidine)-catalyzed addition of bromonitromethane with a high degree of enantioselection. This allows for the production of a range of protected α-bromo nitroalkane donors (including Fmoc) for use in
