Chemical Synthesis

Methyl Methanesulfonate

Methyl Methanesulfonate

Methyl Methanesulfonate

Methyl Methanesulfonate

Methyl Methanesulfonate

Methyl Methanesulfonate

As a co-catalyst with L-proline improved both yield and enantioselectivity of an asymmetric aldol condensation between dioxanones and aldehydes.Efficient catalyst for the preparation of tetrahydropyranyl ethers.

As a co-catalyst with L-proline improved both yield and enantioselectivity of an asymmetric aldol condensation between dioxanones and aldehydes.Efficient catalyst for the preparation of tetrahydropyranyl ethers.

As a co-catalyst with L-proline improved both yield and enantioselectivity of an asymmetric aldol condensation between dioxanones and aldehydes.Efficient catalyst for the preparation of tetrahydropyranyl ethers.

As a co-catalyst with L-proline improved both yield and enantioselectivity of an asymmetric aldol condensation between dioxanones and aldehydes.Efficient catalyst for the preparation of tetrahydropyranyl ethers.

Stannous bromide acts a lewis acid. It is used to prepare alkyl tin compounds and in the spectrophotometric determination of iridium. It is involved in regioselective mono-etherfications of vicinal diols with diazo compounds. It acts as a catalyst

Stannous bromide acts a lewis acid. It is used to prepare alkyl tin compounds and in the spectrophotometric determination of iridium. It is involved in regioselective mono-etherfications of vicinal diols with diazo compounds. It acts as a catalyst