benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate

Base Information

Chemical Name:benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate
CAS No.:1533407-72-5
Molecular Formula:C₃₀H₄₀N₂O₁₄S
Molecular Weight:684.719
Hs Code.:

benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate

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Chemical Property of benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate

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Technology Process of benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate

There total 1 articles about benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

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Reference yield:

: 1533407-53-2
benzyl 2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)acrylate

: 343925-61-1
(2R,3S,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-mercaptotetrahydro-2H-pyran-3,4-diyl diacetate

: 1533407-70-3
C₃₀H₄₀N₂O₁₄S

: 1533407-72-5
benzyl (2S)-2-((4S,5R)-4,5-dimethyl-4-hydroxy-5-methoxy-2-oxooxazolidin-3-yl)-3-(tri-O-acetyl-2-acetamido-2-deoxy-α-D-glucosylthio)propanoate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; at -78 ℃; for 3h; Overall yield = 71 %; Overall yield = 411 mg; diastereoselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1021/ja411522f