70671-47-5Relevant articles and documents
Improved stereoselectivity in intramolecular SN2′ cyclization through use of mechanistic principles
Woo, Duck Seo,Curtis-Long, Marcus J.,Seong, Hun Jeong,Tae, Hong Jun,Min, Suk Yang,Ki, Hun Park
, p. 209 - 214 (2007/10/03)
Valine and alanine were converted into the corresponding α-hydroxy-β-amino acids through intramolecular SN2′ cyclization. The novel cyclization protocol relied upon the use of N-benzyl-protected carbamates derived from α-amino acids. Georg Thie
Stereocontrolled asymmetric synthesis of α-hydroxy-β-amino acids. A stereodivergent approach
Aoyagi,Jain,Williams
, p. 3472 - 3477 (2007/10/03)
The stereocontrolled asymmetric synthesis of α-hydroxy-β-amino acids has been investigated via the Lewis acid-promoted cyanation of (5R,6S)-2-acetoxy-4-(benzyloxycarbonyl)-5, 6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazines with trimethylsilyl cyanide. Base-
Synthesis of 'D-Isothreonine' and 'L-Alloisothreonine' Starting form L-Alanine
Wolf, Jean-Pierre,Pfander, Hanspeter
, p. 116 - 120 (2007/10/02)
Starting from L-alanine, 'D-isothreonine' (=(2R,3S)-3-amino-2-hydroxybutanoic acid) and 'L-alloisothreonine' (=(2S,3S)-3-amino-2-hydroxybutanoic acid) were synthesized.