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N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester

Base Information Edit
  • Chemical Name:N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester
  • CAS No.:250137-68-9
  • Molecular Formula:C18H25NO6
  • Molecular Weight:351.4
  • Hs Code.:
  • Mol file:250137-68-9.mol
N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester

Synonyms:N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester

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Chemical Property of N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester Edit
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Technology Process of N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester

There total 1 articles about N-benzyl-N'-[(1S)-2-hydroxy-1-methylethyl]-(2R,3R)-2,3-di-isopropylidenetartramic acid methyl ester 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 N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In dichloromethane; at 25 ℃; for 12h;
DOI:10.1021/jo9904967
Guidance literature:
Multi-step reaction with 2 steps
1: 90 percent / (COCl)2; DMSO / CH2Cl2 / 0.25 h / -60 °C
2: 85 percent / H2SO4*SiO2 / toluene / 0.33 h / Heating
With oxalyl dichloride; sulfuric acid; dimethyl sulfoxide; In dichloromethane; toluene; 1: Oxidation / 2: Cyclization;
DOI:10.1021/jo9904967
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