197449-36-8

Upstream product

• 150-76-5 4-methoxy-phenol 
• 2873-29-2 D-glucal triacetate 
• 76223-29-5 4'-methoxyphenyl 4,6-di-O-acetyl-2,3-dideoxy-1-O-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 1310542-89-2 C₁₃H₁₄O₅ 
• 1310542-97-2 C₁₈H₂₂O₆ 
• 1449491-86-4 p-methoxyphenyl 2,3-anhydro-6-O-(tert-butyldimethylsilyl)-α-D-allopyranoside 
• 1449491-96-6 C₁₆H₂₃NO₇ 
• 1449491-92-2 C₂₂H₃₅N₃O₇Si 
• 1449491-95-5 2-methyl-1'-O-methoxyphenyl-4'-O-methyl-6'-O-(tert-butyldimethylsilyl)-α-D-mannopyrano[2',3']-Δ2-oxazoline 
• 1449491-94-4 p-methoxyphenyl 2,3-(acetylepimino)-6-O-(tert-butyldimethylsilyl)-4-O-methyl-2,3-dideoxy-α-D-glucopyranoside 
• 1449491-93-3 p-methoxyphenyl 6-O-(tert-butyldimethylsilyl)-4-O-methyl-2-deoxy-2-azido-α-D-altropyranoside 
• 1449491-91-1 p-methoxyphenyl 6-O-(tert-butyldimethylsilyl)-4-O-methyl-3-deoxy-3-azido-α-D-glucopyranoside 
• 1449491-90-0 p-methoxyphenyl 2,3-anhydro-6-O-(tert-butyldimethylsilyl)-4-O-methyl-α-D-allopyranoside 
• 1449491-88-6 p-methoxyphenyl 2,3-anhydro-α-D-allopyranoside 
• 1449491-89-7 p-methoxyphenyl 2,3-anhydro-α-D-mannopyranoside 
• 197449-37-9 p-methoxyphenyl 6-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1241380-56-2 p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-α-D-erythro-hex-2-enopyranoside 

Relevant academic research and scientific papers

2,3-Dideoxy hex-2-enopyranosid-4-uloses as promising new anti-tubercular agents: Design, synthesis, biological evaluation and SAR studies

The alarming resurgence of tuberculosis (TB) underlines the urgent need for development of new and potent anti-TB drugs. Towards this goal we herein report the design and synthesis of 2,3-dideoxy hex-2-enopyranosid-4-uloses as promising new anti-tubercula

A Chemo-Enzymatic Synthesis of D-Allosamine Derivatives from Tri-O-acetyl- D-glucal

N-Acetyl-D-allosamine and its derivatives were synthesized from tri-O-acetyl-D-glucal based on lipase-catalyzed selective protection of primary alcohols, [3,3] sigmatropic rearrangement of allylic trichloroacetimidates, and stereo- selective ruthenium-catalyzed dihydroxylation. In the course of this study, it was revealed that the Pseudomonas lipase- catalyzed acetylation occurred in a high yield (> 90%) exclusively at the primary alcohols of three Ferrier rearrangement products derived from tri-O-acetyl-D-glucal.