4-ethenyloxane

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OsO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OsO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure

Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil. was added After stirring for 60 minutes the mixture was stirred overnight to warm to ambient temperature the layers were separated The aqueous layer was extracted with CH2Cl2 (3×30 mL) the combined organic layers were dried over Na2SO4 filtered concentrated under reduced pressure