116079-35-7

Upstream product

• 98-54-4 para-tert-butylphenol 
• 95715-87-0 (R)-3-tert-butoxycarbonyl-4-formyl-2,2-dimethyloxazolidine 

Downstream Products

• 925704-34-3 (1R,2R)-1-(2-allyloxy-5-tert-butylphenyl)-2-(tert-butoxycarbonylamino)propane-1,3-diyl bis(2,2,2-trichloroacetimidate) 
• 925704-04-7 tert-butyl (1R,2R)-1-(5-tert-butyl-2-(allyloxy)phenyl)-1,3-dihydroxypropan-2-ylcarbamate 

Relevant academic research and scientific papers

Synthesis of protected chiral vicinal diaminoalcohols by diastereoselective intramolecular benzylic substitution from bistrichloroacetimidates

(Chemical Equation Presented) An efficient synthesis of chiral dihydrooxazines (2) from 1-aryl-2-amino-propane-1,3-diols (1) via the corresponding bistrichloroacetimidate intermediates has been developed. In this transformation, one trichloroacetimidate a

Synthesis of 1-(2-Hydroxyaryl)-1,2,3-propanetriol and 1-(2-Hydroxyaryl)-2-amino-1,3-propanediol Derivatives of either threo or erythro Configuration

The title arylglycerols 3A and 4A and arylaminopropanediols 3B and 4B, in either optical series (D or L) and with either configuration (threo or erythro), were prepared in optically pure form by direct arylation of 2,3-O-isopropylidene-D- or -L-glyceralde