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Group 7 metal-promoted oxidations epoxidation by salen manganese complexes

Group 7 metal-promoted oxidations epoxidation by salen manganese complexes [Pg.17]

Preparation of (1S,2/7)-1,2-epoxy-1,2,3,4 tetrahycb onaphthaiene (Structure 16). Asymmetric epoxidation using NaOCl catalysed by Jacobsen s chiral manganese salen complex (Structure 17), [Pg.17]

Caution Employ the standard precautions outlined in the introduction to this chapter for this reaction. [Pg.17]

Clean all glassware sequentially in soap solution, water, and acetone. Allow the acetone to evaporate and then dry the glassware in an electric oven (105 0 for at least 1 h. [Pg.18]

Place 13 mL of sodium hypochlorite solution (NaOCI, ca. 0.8 M) in a 50 mL Erlenmeyer flask. Buffer this by adding 5 mL of sodium phosphate (Na2HP04) solution (0.05 M) and adjust the pH of the solution to about 11 using a few drops of 1 M NaOH. Cool the solution in an ice-water bath. [Pg.18]




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Complex groups, oxides

Complex metal oxides

Complexation by metals

Epoxidation oxidant

Epoxide group

Epoxide oxidation

Epoxides complex

Epoxides metalation

Epoxides oxidation

Group 5 metal complex

Group oxides

Manganese complexes

Manganese complexes oxidation

Manganese complexes oxides

Manganese complexing

Manganese epoxidation

Manganese oxidation

Manganese oxidation epoxidation

Manganese oxidation metal oxides

Manganese promoted

Manganese-oxidizing

Manganese-salen complex

Metal epoxidations

Metallated epoxides

Metals manganese

Oxidants manganese

Oxides group 14 metals

Oxidizing group

Promoter complex

Promoters oxidation

Salen

Salen complexes

Salen metalated

Salens

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