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(4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal

Base Information
  • Chemical Name:(4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal
  • CAS No.:81823-42-9
  • Molecular Formula:C16H25O5P
  • Molecular Weight:328.345
  • Hs Code.:
(4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal

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Chemical Property of (4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal
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Technology Process of (4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal

There total 10 articles about (4R,S)-4,5-dideoxy-2,3-O-isopropylidene-4-C-<(R,S)-phenylphosphinyl>-D-erythro-pentose dimethyl acetal 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 5 steps
1: 71 percent / cadmium carbonate, mercuric chloride / methanol / 19 h / Heating
2: 45 percent / pyridinium chlorochromate, sodium acetate / 168 h / Ambient temperature
3: 19 percent / 1,8-diazabicyclo<5.4.0>-undec-7-ene / 27 h / 20 °C
4: 14 percent / hydrogen / Raney Ni (W-4) / ethanol / 46 h
5: sodium bis(2-methoxyethoxy)aluminate (SDMA) / toluene / 0.17 h / 0 °C
With cadmium(II) carbonate; hydrogen; sodium acetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium bis(2-methoxyethoxy)aluminium dihydride; pyridinium chlorochromate; mercury dichloride; Raney Ni (W-4); In methanol; ethanol; toluene;
DOI:10.1016/S0008-6215(00)88061-1
Guidance literature:
Multi-step reaction with 3 steps
1: 19 percent / 1,8-diazabicyclo<5.4.0>-undec-7-ene / 27 h / 20 °C
2: 14 percent / hydrogen / Raney Ni (W-4) / ethanol / 46 h
3: sodium bis(2-methoxyethoxy)aluminate (SDMA) / toluene / 0.17 h / 0 °C
With hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium bis(2-methoxyethoxy)aluminium dihydride; Raney Ni (W-4); In ethanol; toluene;
DOI:10.1016/S0008-6215(00)88061-1
Guidance literature:
Multi-step reaction with 4 steps
1: 45 percent / pyridinium chlorochromate, sodium acetate / 168 h / Ambient temperature
2: 19 percent / 1,8-diazabicyclo<5.4.0>-undec-7-ene / 27 h / 20 °C
3: 14 percent / hydrogen / Raney Ni (W-4) / ethanol / 46 h
4: sodium bis(2-methoxyethoxy)aluminate (SDMA) / toluene / 0.17 h / 0 °C
With hydrogen; sodium acetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium bis(2-methoxyethoxy)aluminium dihydride; pyridinium chlorochromate; Raney Ni (W-4); In ethanol; toluene;
DOI:10.1016/S0008-6215(00)88061-1
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