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(-)-tamandarin B

Base Information
  • Chemical Name:(-)-tamandarin B
  • CAS No.:258339-38-7
  • Molecular Formula:C53H83N7O14
  • Molecular Weight:1042.28
  • Hs Code.:
(-)-tamandarin B

Synonyms:(-)-tamandarin B

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Chemical Property of (-)-tamandarin B
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Technology Process of (-)-tamandarin B

There total 21 articles about (-)-tamandarin B 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 14 steps
1: 95 percent / EDAC*HCl; DMAP / CH2Cl2 / 0 - 20 °C
2: 83 percent / tetrahydrofuran / -78 °C
3: 77 percent / potassium borohydride / methanol / -30 - 0 °C
4: 82 percent / 2,6-lutidine / CH2Cl2 / 20 °C
5: 81 percent / aq. NaOH / tetrahydrofuran; methanol / 0 - 20 °C
6: 60 percent / EDAC*HCl; DMAP / CH2Cl2 / 0 - 20 °C
7: 100 percent / Pd(PPh3)4; morpholine / tetrahydrofuran / 20 °C
8: Pyr / CH2Cl2
9: 79 percent / DIEA; DMAP / CH2Cl2 / 0 - 20 °C
10: MgBr2*Et2O / CH2Cl2 / -15 - 0 °C
11: H2 / Pd/C / ethyl acetate; methanol / 20 °C
12: HATU; DIEA / dimethylformamide / 20 °C
13: HCl(g) / ethyl acetate / -30 - 0 °C
14: 0.0065 g / DEPBT; DIEA / CH2Cl2 / 15 h / 20 °C
With morpholine; pyridine; 2,6-dimethylpyridine; hydrogenchloride; dmap; sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); potassium borohydride; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ja010222c
Guidance literature:
Multi-step reaction with 7 steps
1: 98 percent / H2 / Pd/C / methanol; ethyl acetate / 5 h
2: 79 percent / DIEA; DMAP / CH2Cl2 / 0 - 20 °C
3: MgBr2*Et2O / CH2Cl2 / -15 - 0 °C
4: H2 / Pd/C / ethyl acetate; methanol / 20 °C
5: HATU; DIEA / dimethylformamide / 20 °C
6: HCl(g) / ethyl acetate / -30 - 0 °C
7: 0.0065 g / DEPBT; DIEA / CH2Cl2 / 15 h / 20 °C
With hydrogenchloride; dmap; hydrogen; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ja010222c
Guidance literature:
Multi-step reaction with 9 steps
1: 60 percent / EDAC*HCl; DMAP / CH2Cl2 / 0 - 20 °C
2: 100 percent / Pd(PPh3)4; morpholine / tetrahydrofuran / 20 °C
3: Pyr / CH2Cl2
4: 79 percent / DIEA; DMAP / CH2Cl2 / 0 - 20 °C
5: MgBr2*Et2O / CH2Cl2 / -15 - 0 °C
6: H2 / Pd/C / ethyl acetate; methanol / 20 °C
7: HATU; DIEA / dimethylformamide / 20 °C
8: HCl(g) / ethyl acetate / -30 - 0 °C
9: 0.0065 g / DEPBT; DIEA / CH2Cl2 / 15 h / 20 °C
With morpholine; pyridine; hydrogenchloride; dmap; tetrakis(triphenylphosphine) palladium(0); hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ja010222c
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