Patent classifications
C07C409/16
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.
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.
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.
Additive composition
The invention relates to a composition obtained by the adsorption of a liquid peroxide onto granules comprising an antioxidant and an acid scavenger, for example wherein the adsorption of the liquid peroxide onto the granules is performed by a process which can be performed at room temperature (23° C.) and the process does not require heating.
Additive composition
The invention relates to a composition obtained by the adsorption of a liquid peroxide onto granules comprising an antioxidant and an acid scavenger, for example wherein the adsorption of the liquid peroxide onto the granules is performed by a process which can be performed at room temperature (23° C.) and the process does not require heating.
ADDITIVE COMPOSITION
The invention relates to a composition obtained by the adsorption of a liquid peroxide onto granules comprising an antioxidant and an acid scavenger, for example wherein the adsorption of the liquid peroxide onto the granules is performed by a process which can be performed at room temperature (23° C.) and the process does not require heating.
ADDITIVE COMPOSITION
The invention relates to a composition obtained by the adsorption of a liquid peroxide onto granules comprising an antioxidant and an acid scavenger, for example wherein the adsorption of the liquid peroxide onto the granules is performed by a process which can be performed at room temperature (23° C.) and the process does not require heating.
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.
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.
PROCESS FOR THE PREPARATION OF FLUORINATED PEROXIDES
The present invention relates to the preparation of perfluorinated or partially fluorinated peroxides which avoids the use of carbonyl fluoride (COF.sub.2).