873783-10-9

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 621-37-4 m-hydroxyphenylacetic acid 
• 899799-11-2 2-[3-(tert-butyldimethylsilanyloxy)phenyl]-1-(3-(S)-tert-butyl-1,1-dioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-ethanone 
• 114774-44-6 (3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)acetic acid 
• 899799-13-4 2-(S)-azido-2-[3-(tert-butyldimethylsilanyloxy)phenyl]-1-(3-(S)-tert-butyl-1,1-dioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)ethanone 

Downstream Products

• 873783-11-0 (S,S,S)-2-{[3,5-bis({4-[3-(tert-butyl(dimethyl)silanyloxy)phenyl]-4,5-dihydrooxazol-2-yl}methyl)-2,4,6-trimethyl]phenyl}methyl-4-[3-(tert-butyl(dimethyl)silanyloxy)phenyl]-4,5-dihydrooxazole 
• 873783-14-3 (S,S,S)-2-{[3,5-bis({4-[3-(tert-butyl(dimethyl)silanyloxy)phenyl]-4,5-dihydrooxazol-2-yl}methyl)-2,4,6-triethyl]phenyl}methyl-4-[3-(tert-butyl(dimethyl)silanyloxy)phenyl]-4,5-dihydrooxazole 

Relevant academic research and scientific papers

An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines

A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from aryla