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dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

Base Information
  • Chemical Name:dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate
  • CAS No.:873550-86-8
  • Molecular Formula:C21H26N3O6P
  • Molecular Weight:447.428
  • Hs Code.:
dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

Synonyms:dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

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Chemical Property of dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate
Chemical Property:
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Technology Process of dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

There total 4 articles about dibenzyl (1R,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate 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:
Multi-step reaction with 2 steps
1: oxalyl chloride; DMSO; Et3N / CH2Cl2 / -70 - 0 °C
2: 15 percent / Et3N / 24 h / 20 °C
With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; 1: Swern oxidation;
DOI:10.1016/j.tet.2005.09.057
Guidance literature:
Multi-step reaction with 3 steps
1: 98 percent / LiCl; NaBH4 / tetrahydrofuran; ethanol / 24 h / 20 °C
2: oxalyl chloride; DMSO; Et3N / CH2Cl2 / -70 - 0 °C
3: 15 percent / Et3N / 24 h / 20 °C
With sodium tetrahydroborate; oxalyl dichloride; dimethyl sulfoxide; triethylamine; lithium chloride; In tetrahydrofuran; ethanol; dichloromethane; 2: Swern oxidation;
DOI:10.1016/j.tet.2005.09.057
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