Patent classifications
C07C29/00
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.
METHOD, APPARATUS, AND SYSTEM FOR PROVIDING AN INTEGRATED BIOENERGY COMPLEX TO PROCESS MIXED SOLID WASTE
An approach is provided for processing mixed solid waste using an integrated bioenergy complex. The approach, for instance, involves receiving the mixed solid waste at the integrated bioenergy complex, the integrated bioenergy complex including an organic conversion processing center and an inorganic conversion processing center. The approach also involves separating the mixed solid waste into recyclables, an organic waste stream, and an inorganic waste stream. The approach further involves feeding the organic waste stream to the organic conversion processing center to produce organic conversion products and an organic residual, and feeding the organic residual and the inorganic waste stream to the inorganic conversion processing center to produce inorganic conversion products, electric power, and a residual waste. The electric power is used to partially or fully power the organic conversion processing center, and residual waste is less than a target percentage of the received mixed solid waste.
METHOD, APPARATUS, AND SYSTEM FOR PROVIDING AN INTEGRATED BIOENERGY COMPLEX TO PROCESS MIXED SOLID WASTE
An approach is provided for processing mixed solid waste using an integrated bioenergy complex. The approach, for instance, involves receiving the mixed solid waste at the integrated bioenergy complex, the integrated bioenergy complex including an organic conversion processing center and an inorganic conversion processing center. The approach also involves separating the mixed solid waste into recyclables, an organic waste stream, and an inorganic waste stream. The approach further involves feeding the organic waste stream to the organic conversion processing center to produce organic conversion products and an organic residual, and feeding the organic residual and the inorganic waste stream to the inorganic conversion processing center to produce inorganic conversion products, electric power, and a residual waste. The electric power is used to partially or fully power the organic conversion processing center, and residual waste is less than a target percentage of the received mixed solid waste.
Recyclable metathesis catalysts
Highly active, recoverable and recyclable transition metal-based metathesis catalysts and their organometallic complexes including dendrimeric complexes are disclosed, including a Ru complex bearing a 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene and styrenyl ether ligand. The heterocyclic ligand significantly enhances the catalytic activity, and the styrenyl ether allows for the easy recovery of the Ru complex. Derivatized catalysts capable of being immobilized on substrate surfaces are also disclosed. The present catalysts can be used to catalyze ring-closing metathesis (RCM), ring-opening (ROM) and cross metatheses (CM) reactions, and promote the efficient formation of various trisubstituted olefins at ambient temperature in high yield.
Recyclable metathesis catalysts
Highly active, recoverable and recyclable transition metal-based metathesis catalysts and their organometallic complexes including dendrimeric complexes are disclosed, including a Ru complex bearing a 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene and styrenyl ether ligand. The heterocyclic ligand significantly enhances the catalytic activity, and the styrenyl ether allows for the easy recovery of the Ru complex. Derivatized catalysts capable of being immobilized on substrate surfaces are also disclosed. The present catalysts can be used to catalyze ring-closing metathesis (RCM), ring-opening (ROM) and cross metatheses (CM) reactions, and promote the efficient formation of various trisubstituted olefins at ambient temperature in high yield.
Recyclable metathesis catalysts
Highly active, recoverable and recyclable transition metal-based metathesis catalysts and their organometallic complexes including dendrimeric complexes are disclosed, including a Ru complex bearing a 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene and styrenyl ether ligand. The heterocyclic ligand significantly enhances the catalytic activity, and the styrenyl ether allows for the easy recovery of the Ru complex. Derivatized catalysts capable of being immobilized on substrate surfaces are also disclosed. The present catalysts can be used to catalyze ring-closing metathesis (RCM), ring-opening (ROM) and cross metatheses (CM) reactions, and promote the efficient formation of various trisubstituted olefins at ambient temperature in high yield.
Neo-alcohol compounds, processes for making same and use thereof
This disclosure relates to neo-alcohol compounds derivable from neo-acids, use of such neo-alcohol compounds, and processes for making neo-alcohol products.
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.