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13,14,15,16-tetranorlabd-8(17)-en-12-ol

Base Information
  • Chemical Name:13,14,15,16-tetranorlabd-8(17)-en-12-ol
  • CAS No.:31207-72-4
  • Molecular Formula:C16H28O
  • Molecular Weight:236.398
  • Hs Code.:
13,14,15,16-tetranorlabd-8<sup>(17)</sup>-en-12-ol

Synonyms:13,14,15,16-tetranorlabd-8(17)-en-12-ol

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Chemical Property of 13,14,15,16-tetranorlabd-8(17)-en-12-ol
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Technology Process of 13,14,15,16-tetranorlabd-8(17)-en-12-ol

There total 2 articles about 13,14,15,16-tetranorlabd-8(17)-en-12-ol 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 3 steps
1: KMnO4; MgSO4 / acetone / 20 °C
2: 66 percent / oxygen / 1,2-dimethoxy-ethane / 4 h / 20 °C
3: 95 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
With potassium permanganate; lithium aluminium tetrahydride; oxygen; magnesium sulfate; In tetrahydrofuran; 1,2-dimethoxyethane; acetone;
DOI:10.1080/00397910500377172
Guidance literature:
Multi-step reaction with 8 steps
1: 5 g / t-butyl hydroperoxide, vanadyl acetylacetonate / benzene
2: 4.7 g / LiAlH4 / diethyl ether / 1 h / Heating
3: 3.5 g / sodium periodate / H2O; methanol / Ambient temperature
4: 3.2 g / sodium hypobromite / dioxane
5: 0.57 g / LDA, diperoxo(oxohexamethylphosphoramido)molybdenum(VI) / tetrahydrofuran; hexane / 2 h / -5 °C
6: 0.6 g / LiAlH4 / diethyl ether / 1 h / Heating
7: 0.1 g / sodium periodate / H2O; methanol / Ambient temperature
8: 0.09 g / LiAlH4 / diethyl ether / 0.5 h / Heating
With tert.-butylhydroperoxide; sodium periodate; lithium aluminium tetrahydride; sodium hypobromide; diperoxo(oxohexamethylphosphoramido)molybdenum(VI); vanadyl acetylacetonate; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; hexane; water; benzene;
DOI:10.1071/CH9880711
Guidance literature:
Multi-step reaction with 2 steps
1: Jones reagent
2: dmap / dichloromethane / 10 h / 20 °C
With dmap; Jones reagent; In dichloromethane;
DOI:10.1055/s-0032-1318253
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