methoxide

Sodium methoxide is produced on an industrial scale and available from a number of chemical companies.

Sodium methoxide as catalyst produced a rate ratio of 73:1.

Treatment of either 25a or25b with sodium methoxide results cleanly in N2-deacylation to give compound 26.

These compounds, treated with sodium methoxide, lead to 3,4-fluorinated pyrroles.

The methoxide/methanol treatment of the 4-trichloroacetylated intermediate leads to methyl 2-formylpyrrole-4-carboxylate.

The most widely used base is sodium methoxide.

None of the epoxides examined in this study reacted with magnesium methoxide.

The (R)-dipentanoate is hydrolysed in a second step with sodium methoxide.

The reaction mechanism starts with an attack on the carbonyl group by a strong base, such as methoxide ion.

A methoxide group attacks the boron atom giving a borate complex which fragments.

This represents the rapid expulsion of methoxide from the conjugate base of 5.

Treatment of the title compound, 2, with excess sodium methoxide produced an unsaturated secondary alcohol, 3.

Freshly prepared sodium methoxide in methanol is commonly used to effect rearrangement without opening.

The structure, and hence its basicity, of sodium methoxide in solution depends on the solvent.

Upon treatment with a standard base, complexes with a weak contribution convert to a metal methoxide.

Under these excess conditions, methoxide also causes a faster rate of displacement than does tert-butoxide as nucleophile.

The cellulosate was prepared insitu from microcrystalline cellulose and sodium methoxide.

The Grob fragmentation to 6 takes place with sodium methoxide in methanol at reflux.

Anhydrous base such as sodium methoxide in methanol.

This transformation is catalyzed by sodium methoxide.

Potassium methoxide is commonly used as a catalyst for transesterification in the production of biodiesel.

Sodium methoxide is added to generate Hagemann's ester.

Alkylation of the enol with sodium methoxide and 3-dimethylaminopropyl chloride gives benzydamine.

Sodium methoxide is prepared by carefully treating methanol with sodium:

Upon treated with sodium methoxide, it releases CCl.