767344-26-3Relevant academic research and scientific papers
Synthesis of alkylated sugar amino acids: Conformationally restricted l-Xaa-l-Ser/Thr mimics
Risseeuw, Martijn D.P.,Mazurek, Jaroslaw,Van Langenvelde, Arjan,Van Der Marel, Gijsbert A.,Overkleeft, Herman S.,Overhand, Mark
, p. 2311 - 2314 (2008/02/14)
Two synthetic strategies for the generation of δ-substituted pyranoid sugar amino acids (SAAs) are evaluated. The first employs chiral nonracemic tert-butane sulfinamides as key reagents. Regardless of the stereochemistry of the applied sulfinamide, the p
Alkylated sugar amino acids: A new entry toward highly functionalized dipeptide isosters
Raunkjaer, Michael,Oualid, Farid El,Van Der Marel, Gijs A.,Overkleeft, Herman S.,Overhand, Mark
, p. 3167 - 3170 (2007/10/03)
(Chemical Equation Presented) Novel highly functionalized dipeptide isosters are synthesized via a diastereoselective alkyl/arylation protocol of a glucose-derived (R)-tertbutanesulfinylimine. One of these novel sugar amino acid derivatives, a D-Ala-Ser/T
