168211-10-7Relevant academic research and scientific papers
Asymmetric synthesis of (2R,3S)-4-halo-3-benzyloxy-2-(N-methoxycarbonyl-N-benzylamino)butyronitriles as precursors for the synthesis of β-hydroxy-α-amino acids
Badorrey, Ramon,Cativiela, Carlos,Diaz-De-Villegas, Maria D.,Galvez, Jose A.
, p. 1015 - 1025 (2007/10/03)
(2R,3S)-4-Halo-3-benzyloxy-2-(N-methoxycarbonyl-N-benzylamino)butyronitriles have been prepared through an efficient three-step sequence from (2R,3S)-2-benzylamino-3-benzyloxy-4-(tert-butyldimethylsilyloxy)butyronitrile, which is readily available in dias
Diastereoselective strecker reaction of D-glyceraldehyde derivatives. A novel route to (2S,3S)- and (2R,3S)-2-amino-3,4-dihydroxybutyric acid
Cativiela, Carlos,Diaz-De-Villegas, Maria D,Galvez, Jose A.,Garcia, Jose I.
, p. 9563 - 9574 (2007/10/03)
Efficient and stereoselective synthetic routes to enantiomerically pure (2S,3S)- and (2S,3S)-2-amino-3,4-dihydroxybutyric acid have been developed using the stereoselective Strecker type reaction of carbonyl compounds derived from appropriately protected
Diastereoselective Strecker Reaction of Imines Derived from D-Glyceraldehyde. A New Route to β-hydroxy-α-amino acids
Cativiela, Carlos,Diaz-de-Villegas, Maria D.,Galvez, Jose A.
, p. 2859 - 2860 (2007/10/02)
A diastereoselective Strecker type reaction of imines derived from conveniently protected D-glyceraldehyde has been achieved with good to excellent stereoselectivity through an appropriate choice of the protecting group and reaction conditions.
