106943-08-2Relevant academic research and scientific papers
Reductive Acylation of α-Keto Azides Derived from L-Amino Acids using N-Protected L-Aminothiocarboxylic S-Acids
McKervey, M. Anthony,O'Sullivan, Michael B.,Myers, Peter L.,Green, Richard H.
, p. 94 - 96 (1993)
Several homochiral N-protected α-aminothiocarboxylic S-acids have been synthesised from natural amino acids and used for reductive acylation of homochiral α,α'-amino keto azides, also derived from natural amino acids.
Stereoselective reduction of N-phthaloyl α-amino ketones: An expeditious new synthesis of non-racemic threo-α-amino epoxides
Sengupta, Saumitra,Sarma, Debarati Sen,Das, Debasis
, p. 1653 - 1659 (2007/10/03)
Enantiopure α-diazoketones derived from N-Pht amino acids have been converted to threo-α-amino epoxides via HBr treatment followed by a highly syn-selective reduction with LiA1H(OBu-t)3.
SULFUR YLIDES. 3. SYNTHESIS OF KETO-GROUP STABILIZED AMINO-CONTAINING SULFUR YLIDES FROM AMINO ACIDS
Tolstikov, G. A.,Galin, F. Z.,Lakeev, S. N.,Khalilov, L. M.,Sultanova, V. S.
, p. 535 - 541 (2007/10/02)
An effective path of synthesis was developed of new synthetic intermediates, the optically active, keto-group stabilized amino-substituted sulfur ylides.
