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(2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone

Base Information
  • Chemical Name:(2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone
  • CAS No.:1187848-75-4
  • Molecular Formula:C14H18O2
  • Molecular Weight:218.296
  • Hs Code.:
(2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone

Synonyms:(2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone

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Chemical Property of (2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone
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Technology Process of (2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone

There total 8 articles about (2S,3S)-2-benzyl-3-hydroxy-2-methylcyclohexanone 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 C42H51F5NO3P; N-ethyl-N,N-diisopropylamine; benzo[1,3,2]dioxaborole; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jacs.1c00277
Guidance literature:
With D-glucose; Bacillus megaterium glucose dehydrogenase; recombinant Ogataea glucozyma ketoreductase KRED1-Pglu; nicotinamide adenine dinucleotide phosphate; In dimethyl sulfoxide; for 24h; pH=8.0; stereoselective reaction; Enzymatic reaction;
DOI:10.1007/s10562-019-03015-y
Guidance literature:
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; f-ampha; hydrogen; sodium t-butanolate; In dichloromethane; at 20 ℃; for 14h; under 30402 Torr; Overall yield = 83 %; stereoselective reaction;
DOI:10.1039/c9sc01769k
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