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Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester

Base Information
  • Chemical Name:Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester
  • CAS No.:136409-07-9
  • Molecular Formula:C18H21NO7
  • Molecular Weight:363.367
  • Hs Code.:
Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester

Synonyms:Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester

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Chemical Property of Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester
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Technology Process of Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester

There total 2 articles about Benzyl-2-acetamido-3-O-acetyl-2,4-didesoxy-β-L-threo-hex-4-enopyranosiduronsaeure-methylester 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:

synthetic route:
Guidance literature:
With 7-methyl-1,3,5-triazabicyclo<4.4.0>dec-5-ene; 3 A molecular sieve; In toluene; for 1.83333h; Heating;
Guidance literature:
Multi-step reaction with 3 steps
1: 29 percent / H2 / 10percent Pd/C / methanol / 48 h / 760 Torr
2: 1) hydroxylamine hydrochloride, 1 N NaOMe / 1) EtOH, 50 deg C, 2) 50 deg C, 1 h
3: 32 percent / CSA / 20 h / Ambient temperature
With camphor-10-sulfonic acid; hydroxylamine hydrochloride; hydrogen; sodium methylate; palladium on activated charcoal; In methanol;
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