698373-56-7Relevant academic research and scientific papers
Enantioselective synthesis of α-fluoro-β3-amino esters: Synthesis of enantiopure, orthogonally protected α-fluoro- β3-lysine
Duggan, Peter J.,Johnston, Martin,March, Taryn L.
experimental part, p. 7365 - 7372 (2011/02/23)
The scope of a tandem conjugate addition-fluorination sequence performed on α,β-unsaturated esters using the enantiopure lithium amide derived from (S)-N-benzyl-N-(α-methylbenzyl)amine, and the electrophilic fluorinating agent N-fluorobenzenesulfonimide h
Stereoselective synthesis of β-amino-α-fluoro esters via diastereoselective fluorination of enantiopure β-amino enolates
Andrews, Philip C.,Bhaskar, Vijaya,Bromfield, Karen M.,Dodd, Aileen M.,Duggan, Peter J.,Duggan, Sandhya A. M.,McCarthy, Tom D.
, p. 791 - 794 (2007/10/03)
β-Amino-α-fluoro esters have been prepared stereoselectively from t-butyl cinnamate and ethyl crotonate via tandem conjugate addition of lithium (S)-(-)-N-benzyl-N-α-methylbenzylamide, followed by fluorination with N-fluorobenzenesulfonimide. The absolute
