165967-44-2

Upstream product

• 129940-50-7 (S)-tritylglycidol 
• 330555-60-7 (S)-5-triphenylmethoxymethyl-1,3-oxazolidin-2-one 

Downstream Products

• 952507-60-7 (S)-2,2,2-trifluoro-N-(2-hydroxy-3-(trityloxy)propyl)acetamide 
• 1374255-91-0 (S)-2-bromo-N-[2-hydroxy-3-(trityloxy)propyl]acetamide 
• 1374255-92-1 (S)-6-[(trityloxy)methyl]morpholin-3-one 
• 1374255-93-2 (S)-2-(trityloxymethyl)morpholine 
• 952507-64-1 (S)-1-(2,2,2-trifluoroacetamido)-3-(trityloxy)propan-2-yl-methanesulfonate 
• 952507-67-4 (R)-2-(trifluoromethyl)-5-(trityloxymethyl)-oxazoline 

Relevant academic research and scientific papers

Synthesis of chiral 2-oxazolidinones, 2-oxazolines, and their analogs

Chiral five-membered ring 2-oxazolidinones and six-membered ring 1,3-oxazinan-2-ones are synthesized from the corresponding amino alcohols with complete inversion or retention of stereochemistry. Chiral 5-substituted 2-oxazolines and 6-substituted 2-oxazi

SYNTHESIS OF BASE-MODIFIED "ABBREVIATED" NAD ANALOGUES

The "abbreviated" model of NAD, 1--3-carbamoylpyridinium chloride (VIIIa), and its 2,6-diaminopurine (VIIIb), 3-deazaadenine (VIIIc), guanine (VIIId) and cytosine (VIIIe) analogues were prepared by the Zincke reaction.The (R)-isomer of the adenine model VIIIa (compound IX) was prepared for chiroptical studies.As shown by NMR, UV and CD spectra, neither in dimethyl sulfoxide nor in water any intramolecular ?-? interactions exist between the heteroaromatic systems.