Technology Process of C36H33N3O7
There total 8 articles about C36H33N3O7 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
osmium(VIII) oxide; 4-methylmorpholine N-oxide;
In
water; acetone; tert-butyl alcohol;
for 16h;
DOI:10.1021/ja971304x
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 89 percent / LiBH4 / tetrahydrofuran / 0.33 h
2: 71 percent / pyridinium trifluoroacetate, 1,3-dicyclohexylcarbodiimide / benzene; dimethylsulfoxide / 9 h / Ambient temperature
3: 85 percent / BF3*OEt2 / diethyl ether / 24 h / 25 - 30 °C
4: 95 percent / NaBH4 / methanol; CH2Cl2; CHCl3 / 0.08 h
5: 1.) NaH / 1) THF, 25 min; 2) THF, 50 min
6: 88 percent / Martin's sulfurane / CDCl3 / 0.33 h
7: 84 percent / 4-methylmorpholine-N-oxide, OsO4 / 2-methyl-propan-2-ol; acetone; H2O / 16 h
With
sodium tetrahydroborate; osmium(VIII) oxide; lithium borohydride; Martins sulfurane; boron trifluoride diethyl etherate; pyridinium trifluroacetate; sodium hydride; 4-methylmorpholine N-oxide; dicyclohexyl-carbodiimide;
In
tetrahydrofuran; methanol; diethyl ether; chloroform-d1; dichloromethane; chloroform; water; dimethyl sulfoxide; acetone; tert-butyl alcohol; benzene;
DOI:10.1021/ja971304x
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 71 percent / pyridinium trifluoroacetate, 1,3-dicyclohexylcarbodiimide / benzene; dimethylsulfoxide / 9 h / Ambient temperature
2: 85 percent / BF3*OEt2 / diethyl ether / 24 h / 25 - 30 °C
3: 95 percent / NaBH4 / methanol; CH2Cl2; CHCl3 / 0.08 h
4: 1.) NaH / 1) THF, 25 min; 2) THF, 50 min
5: 88 percent / Martin's sulfurane / CDCl3 / 0.33 h
6: 84 percent / 4-methylmorpholine-N-oxide, OsO4 / 2-methyl-propan-2-ol; acetone; H2O / 16 h
With
sodium tetrahydroborate; osmium(VIII) oxide; Martins sulfurane; boron trifluoride diethyl etherate; pyridinium trifluroacetate; sodium hydride; 4-methylmorpholine N-oxide; dicyclohexyl-carbodiimide;
In
methanol; diethyl ether; chloroform-d1; dichloromethane; chloroform; water; dimethyl sulfoxide; acetone; tert-butyl alcohol; benzene;
DOI:10.1021/ja971304x