138715-29-4

Upstream product

• 138715-28-3 (4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone 
• 1077-28-7 Thioctic acid 
• 13880-12-1 5-((3R)-1,2-dithiolan-3-yl)pentanoyl chloride 
• 492-41-1 (1R,2S)-norephedrine 
• 124368-83-8 (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane 
• 138715-25-0 (1S,2R)-N-<2-(tert-butyldimethylsiloxy)-1-methyl-2-phenylethyl>formamide 
• 138715-27-2 (1S,2R)-2-(tert-butyldimethylsiloxy)-1-methyl-2-phenylethyl isoselenocyanate 
• 138715-26-1 (1S,2R)-2-(tert-butyldimethylsiloxy)-1-methyl-2-phenylethyl isocyanide 

Relevant academic research and scientific papers

Synthesis and Characterization of Acylated Chiral Oxazolidine-2-selones: Selone Chiral Derivatizing Agents for the Detection and Quantitation of Remotely Disposed Chiral Centers

Racemic and chiral carboxylic acids and acid chlorides are coupled cleanly to oxazolidine-2-selone chiral derivatizing agents (CDA's) with yields ranging from 85 to 99percent. 77Se NMR spectroscopy provides a highly sensitive method for the determination

Synthesis of (4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone: A Chiral Auxiliary Reagent Capable of Detecting the Enantiomers of (R,S)-Lipoic Acid by 77Se Nuclear Magnetic Resonance Spectroscopy

(4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone was constructed in 5 steps on the 10-gram scale. 77Se NMR spectroscopic studies revealed that this selone served as a remarkably sensitive chiral auxiliary agent which readily distinguished the selone-coup