C07C11/12

Ligand for forming ruthenium complex, ruthenium complex catalyst, production method therefor and use thereof

The present invention relates to a novel ligand for forming a ruthenium complex, a ruthenium complex catalyst, a production method therefor and a use thereof. The ligand for forming a ruthenium complex and the ruthenium complex catalyst, according to the present invention, exhibit high catalytic activity, high selectivity, and stability.

Ligand for forming ruthenium complex, ruthenium complex catalyst, production method therefor and use thereof

The present invention relates to a novel ligand for forming a ruthenium complex, a ruthenium complex catalyst, a production method therefor and a use thereof. The ligand for forming a ruthenium complex and the ruthenium complex catalyst, according to the present invention, exhibit high catalytic activity, high selectivity, and stability.

METHOD FOR PRODUCING SPECIFIC ALPHA, BETA-UNSATURATED ALDEHYDES

The present invention relates to an improved method for producing specific α, β-unsaturated aldehydes.

METHOD FOR PRODUCING SPECIFIC ALPHA, BETA-UNSATURATED ALDEHYDES

The present invention relates to an improved method for producing specific α, β-unsaturated aldehydes.

SELECTIVE PARTIAL HYDROGENATION OF BETA-FARNESENE

Process for preparing an olefinic product comprising partially hydrogenated β-farnesene in two stages. In the first stage, reaction conditions are controlled to favor the hydrogenation of β-farnesene over auto dimerization and polymerization of β-farnesene. In the second stage, reaction conditions are controlled to favor the hydrogenation of dihydro-β-farnesene and tetrahydro-β-farnesene to form hexahydro-β-hydrofarnesene over the hydrogenation of hexahydro-β-hydrofarnesene to form farnesane.

SELECTIVE PARTIAL HYDROGENATION OF BETA-FARNESENE

Process for preparing an olefinic product comprising partially hydrogenated β-farnesene in two stages. In the first stage, reaction conditions are controlled to favor the hydrogenation of β-farnesene over auto dimerization and polymerization of β-farnesene. In the second stage, reaction conditions are controlled to favor the hydrogenation of dihydro-β-farnesene and tetrahydro-β-farnesene to form hexahydro-β-hydrofarnesene over the hydrogenation of hexahydro-β-hydrofarnesene to form farnesane.

SELECTIVE PARTIAL HYDROGENATION OF BETA-FARNESENE

Process for preparing an olefinic product comprising partially hydrogenated β-farnesene in two stages. In the first stage, reaction conditions are controlled to favor the hydrogenation of β-farnesene over auto dimerization and polymerization of β-farnesene. In the second stage, reaction conditions are controlled to favor the hydrogenation of dihydro-β-farnesene and tetrahydro-β-farnesene to form hexahydro-β-hydrofarnesene over the hydrogenation of hexahydro-β-hydrofarnesene to form farnesane.

Hydrocarbon conversion process

The invention relates to a process for converting hydrocarbons into products containing aldehydes and/or alcohols. The invention also relates to producing olefins from the aldehyde and alcohol, to polymerizing the olefins, and to equipment useful for these processes.

Hydrocarbon conversion process

The invention relates to a process for converting hydrocarbons into products containing aldehydes and/or alcohols. The invention also relates to producing olefins from the aldehyde and alcohol, to polymerizing the olefins, and to equipment useful for these processes.

SITE-SPECIFIC ISOTOPIC LABELING OF 1,4-DIENE SYSTEMS

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.