SEARCH Articles Figures Tables 1.3- Oxazine, dihydroreaction with carbonyl compounds two-carbon homologation A-Carbon of carbonyl compounds Addition of Carbon Nucleophiles to Carbonyl Groups Addition to carbon monoxide and metal carbonyls Aliphatic carbonyl carbon Alkane picosecond carbon-hydrogen bond cleavage at the iridium carbonyl center Alkylating the a-Carbon of Carbonyl Compounds Allyl carbonates carbonylation Bridging carbonyls, carbon monoxide adsorbed C2OS3 Carbon disulfide - carbonyl sulfide C3O4S2 Carbon dioxide - carbonyl sulfide C3O5S Carbon dioxide - carbonyl sulfide Carbon 13 chemical shifts carbonyls Carbon Monoxide and Metal Carbonyls Carbon carbonyl chloride Carbon carbonylation with organoboranes Carbon dioxide Carbonyl sulfide Carbon dioxide, supercritical carbonylation Carbon exchange with carbonyls Carbon monoxide Carbonyls Carbon monoxide carbonyl difluoride Carbon monoxide carbonyl-phosphine rhodium Carbon monoxide carbonylation Carbon monoxide double carbonylation Carbon monoxide metal carbonyls Carbon monoxide methanol carbonylation Carbon monoxide nickel carbonyl formation Carbon monoxide s. a. Carbonylation) Carbon monoxide: carbonyl synthon Carbon of carbonyl groups Carbon photoinitiated carbonylations Carbon reaction with, carbonyl difluoride Carbon rhodium carbonyl clusters Carbon steel Carbonyl sulfide Carbon-13 chemical shifts of carbonyl group Carbon-heteroatom bond formation carbonyl compounds Carbon-nitrogen bond formation carbonyl compounds Carbon-phosphorus bond formation carbonyl compounds Carbonate synthesis, alcohol oxidative carbonylations, palladium Carbonic acid Carbonyl complexes Carbonic anhydrases zinc-carbonyl mechanism Carbonyl carbon Carbonyl carbon Carbonyl carbon atom Carbonyl carbon centers, nucleophilic Carbonyl carbon centers, nucleophilic reactions Carbonyl carbon group Carbonyl carbon kinetic isotope effects Carbonyl carbon, formation, deep Carbonyl carbon, nucleophilicity Carbonyl carbon, nucleophilicity order Carbonyl carbon/oxygen double bonds Carbonyl carbons, nucleophilic substitution Carbonyl complexes from carbon monoxide Carbonyl compounds 3-carbon Carbonyl compounds carbon disulfide Carbonyl compounds carbon-centred radicals Carbonyl compounds carbon-chlorine bond formation Carbonyl compounds carbon-oxygen bond cleavage Carbonyl difluoride carbon dioxide Carbonyl group carbon—oxygen bond length Carbonyl groups carbon-13 chemical shifts Carbonyl stabilised carbon anions Carbonyl sulfide/carbon disulfide Carbonyl sulfide/carbon disulfide sulfur recovery) Dimethyl carbonate oxidation carbonylation Dimethyl carbonate reductive carbonylation Electrophilicity of the carbonyl carbon atom Heterogeneous catalysis carbonylation with carbon Ketene chemistry carbonyl carbon Metal-activated carbon catalysts carbonylation Microwave-Promoted Carbonylations Using Reaction Vessels Prepressurized with Carbon Monoxide Microwave-Promoted Carbonylations Using the Solvent as a Source of Carbon Monoxide Migrations to Carbonyl Carbon Nucleophilic Substitution at Carbonyl Carbon Other Reactions at the Carbonyl Carbon Atom Oxidative Carbonylation Diphenyl Carbonate Oxidative Carbonylation of Alcohols to Carbonates, Oxalates, and Carbamates Propargyl carbonates carbonylation Propargylic carbonate carbonylation Reaction of Carbon Nucleophiles with Carbonyl Groups Reactions at Carbonyl Carbon Reactions at the Carbonyl Carbon of Acid Derivatives Reactions at the Carbonyl Group—Adding or Removing One Carbon Atom Reactions at the a Carbon of Carbonyl Compounds Enols and Enolates Reactions of Carbonyl Compounds with Other Carbon Nucleophiles Rhodium complex-catalyzed carbonylation carbon Selectivity in the Reduction of Carbonyl Derivatives Containing a Chiral Carbon Substitution Reactions of Carbonyl Compounds at the a Carbon Substitution in Carbonyls Carbon Monoxide Replacement Sulphur gases Carbonyl sulphide, Carbon Synthesis of carbonyl difluoride from carbon