868367-34-4

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 868367-33-3 carbonic acid allyl ester 6-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-4-p-tolylsulfanyl-hexahydro-pyrano[3,4-d]oxazol-7-yl ester 
• 108-24-7 acetic anhydride 
• 868367-32-2 6-(tert-butyl-diphenyl-silanyloxymethyl)-7-hydroxy-4-p-tolylsulfanyl-tetrahydro-pyrano[3,4-d]oxazol-2-one 

Downstream Products

• 868367-35-5 Carbonic acid (3aR,4R,6R,7S,7aR)-3-acetyl-4-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-pyrano[3,4-d]oxazol-7-yl ester allyl ester 
• 868367-36-6 Carbonic acid allyl ester (3aR,4R,6R,7S,7aR)-4-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-2-oxo-hexahydro-pyrano[3,4-d]oxazol-7-yl ester 

Relevant academic research and scientific papers

Chemoselective deprotection and functional group interconversion of ring-fused 2N,3O-oxazolidinones of N-acetyl-D-glucosamine

These studies describe the chemoselective deprotection of trans-fused 2N,3O-oxazolidinone derivatives of N-acetyl-β-D-glucosamine. Selective opening of the oxazolidinone ring or N-deacetylation without ring opening is demonstrated. Certain amines are show