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(2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone

Base Information
  • Chemical Name:(2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone
  • CAS No.:180184-98-9
  • Molecular Formula:C17H16O3S
  • Molecular Weight:300.378
  • Hs Code.:
(2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone

Synonyms:(2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone

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Chemical Property of (2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone
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Technology Process of (2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone

There total 7 articles about (2S,3S)-trans-2-phenylsulfonyl-3-phenylcyclopentanone 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 (4R,4’R)-2,2’-(propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole); sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate; copper dichloride; In dichloromethane; at 40 ℃; Reagent/catalyst; enantioselective reaction; Reflux; Inert atmosphere;
DOI:10.1016/j.tetasy.2013.09.009
Guidance literature:
With (4R,4’R)-2,2’-(propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole); sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate; copper dichloride; In dichloromethane; for 2h; Reagent/catalyst; enantioselective reaction; Reflux; Inert atmosphere;
DOI:10.1055/s-0033-1340471
Guidance literature:
Multi-step reaction with 4 steps
1: 2.) NaH / 1.) DMSO, THF
2: 60 percent / TsN3, Et3N / ethanol
3: Rh2(OAc)4 / CH2Cl2 / Heating
4: 1.) NaOH, 2.) baker's yeast / 1.) H2O, 2.) H2O
With dirhodium tetraacetate; sodium hydroxide; 4-toluenesulfonyl azide; baker's yeast; sodium hydride; triethylamine; In ethanol; dichloromethane;
DOI:10.1016/S0040-4039(97)01756-5
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