The Hieber anion [Fe(CO)₃(NO)]^-

Keyphrases

• Anions 100%
• Allylic Substitution 100%
• Allyl 80%
• Alcohol 60%
• Nucleophile 60%
• Stereochemistry 60%
• Transesterification 60%
• Allyl Carbonate 60%
• Ipso-substitution 60%
• Ionomycin 40%
• Mesylate 40%
• Acyl 40%
• Carbonylation 40%
• Hydrides 40%
• NHC Ligands 40%
• Thioester 40%
• Ph3P 40%
• Moisture 20%
• Methanol 20%
• Ketones 20%
• Carbon Dioxide 20%
• Elevated Temperature 20%
• Molecular Sieve 20%
• Mechanism-based 20%
• Alkylation 20%
• Product Basis 20%
• Carbonate 20%
• Piperidine 20%
• Aldehydes 20%
• Beneficial Effects 20%
• Esters 20%
• Thioesterification 20%
• Methyl Ester 20%
• Dipeptide 20%
• Aryl 20%
• Methoxide 20%
• Native Chemical Ligation 20%
• Alkyl Halides 20%
• Hydrosilylation 20%
• Phenyl Ester 20%
• Polyketide Natural Products 20%
• Subsequent Reactions 20%
• Secondary Alkyl Halides 20%
• Phosphine Ligands 20%
• O-nucleophiles 20%
• Allyl Phenyl Ether 20%
• Sulfonation 20%
• Selective Formation 20%
• Polymethylhydrosiloxane 20%
• C-nucleophiles 20%
• Chlorophenyl 20%
• Organocuprates 20%
• Excellent Yields 20%
• Carbonyl Compounds 20%
• O-allylation 20%
• Advanced Intermediates 20%
• Stoichiometric Reaction 20%
• Allyl Complexes 20%
• N-nucleophiles 20%
• S-nucleophiles 20%
• Allylic Amination 20%
• Vinyl Acetate 20%
• CO Insertion 20%
• Sodium Sulfinates 20%
• Diastereoisomers 20%
• Crystallization Reaction 20%
• Sulfenylation 20%
• β-hydride Elimination 20%
• Acyl Donor 20%
• Acylate 20%
• Enantiopure 20%
• Branched Products 20%

Chemistry

• Nucleophile 100%
• Stereochemistry 42%
• Transesterification 42%
• Thioester 28%
• Carbonylation 28%
• Halide 28%
• Ionomycin 28%
• Vinyl Acetate 14%
• Ketones 14%
• Methoxide 14%
• Carbonyl Compound 14%
• Enantiopurity 14%
• Dipeptide 14%
• Methyl Ester 14%
• Piperidine 14%
• Absorbent 14%
• Sodium 14%
• Hydrosilylation 14%
• Polyketide 14%
• Acyl Donor 14%
• Sulfinate 14%
• Allylic Amination 14%
• Sulfenylation 14%
• Carbon Monoxide 14%
• formation 14%
• Natural Product 14%
• Alkylation 14%
• sulfonation 14%
• O-allylation of phenols 14%