Tricarbonyl(η5-4-triethylsilyl-1-methylpentadienyl)iron(+1) hexafluorophosphate was prepared by the protonation of γ-endo tricarbonyl (η4-5-triethylsilyl-3,5-hexadien-2-ol)iron with hexafluorophosphoric acid. The cation reacts with H2O, CH3OH, NaBH3CN, PPh3, sodium dimethylmalonate and dimethyl cuprate in a regiospecific fashion by nucleophilic attack at C1. The regioselectivity for nucleophilic attack appears to be predominantly the result of steric control
While (η5 -pentadienyl)iron(1+) cations were first prepared more than 40 years ago, the reactivity o...
The title compounds react with malonate anions by attack at both the substituted and unsubstituted t...
Alkynes add to tricarbony](vinytketene)iron(0) complexes to generate stable 1:1 adducts, the structu...
The title cation 2, prepared by protonation of (5‐methoxy‐3,5‐hexadien‐2‐ol)Fe(CO)3, reacts regio‐ a...
Tricarbonyl(l,2-dimethylpentadienyl)iron(+1) (3a), tricarbonyl(2-methyl- 1-phenylpentadienyl)iron(+l...
The title cation was prepared in two steps from the known (ethyl 3-methyl-6-oxo-2,4-hexadienoate)Fe(...
Tricarbonyl(1-methoxycarbonyl-5-phenylpentadienyl)iron(1+) hexafluorophosphate (7) was prepared in t...
The reactions of 1,2-dimethyl-, 1-phenyl-2-methyl-, 1,4-dimethyl-, and 1-phenyl-4-methyl- substitute...
The use of organoiron complexes has been recognized as a powerful tool in synthetic methodology due ...
The synthesis of (5S,6E,8Z,11Z,14Z)-5-hydroxy-6,8,11, 14-icosatetraenoic acid (5-HETE) methyl ester,...
Summary: Reactions of tricarbonyl(2,4-dimethylpentadienyl)iron(l+) hexafluorophosphate (1) with sodi...
While (η5 -pentadienyl)iron(1+) cations were first prepared more than 40 years ago, the reactivity o...
The title compounds react with alkynyl cuprates via attack at the unsubstituted terminus to afford (...
The use of transition organometallic complexes as reagents for the synthesis of complex organic mole...
In an effort to make diverse molecular complexity from simple hydrocarbons, tricarbonyl(cyclohexadie...
While (η5 -pentadienyl)iron(1+) cations were first prepared more than 40 years ago, the reactivity o...
The title compounds react with malonate anions by attack at both the substituted and unsubstituted t...
Alkynes add to tricarbony](vinytketene)iron(0) complexes to generate stable 1:1 adducts, the structu...
The title cation 2, prepared by protonation of (5‐methoxy‐3,5‐hexadien‐2‐ol)Fe(CO)3, reacts regio‐ a...
Tricarbonyl(l,2-dimethylpentadienyl)iron(+1) (3a), tricarbonyl(2-methyl- 1-phenylpentadienyl)iron(+l...
The title cation was prepared in two steps from the known (ethyl 3-methyl-6-oxo-2,4-hexadienoate)Fe(...
Tricarbonyl(1-methoxycarbonyl-5-phenylpentadienyl)iron(1+) hexafluorophosphate (7) was prepared in t...
The reactions of 1,2-dimethyl-, 1-phenyl-2-methyl-, 1,4-dimethyl-, and 1-phenyl-4-methyl- substitute...
The use of organoiron complexes has been recognized as a powerful tool in synthetic methodology due ...
The synthesis of (5S,6E,8Z,11Z,14Z)-5-hydroxy-6,8,11, 14-icosatetraenoic acid (5-HETE) methyl ester,...
Summary: Reactions of tricarbonyl(2,4-dimethylpentadienyl)iron(l+) hexafluorophosphate (1) with sodi...
While (η5 -pentadienyl)iron(1+) cations were first prepared more than 40 years ago, the reactivity o...
The title compounds react with alkynyl cuprates via attack at the unsubstituted terminus to afford (...
The use of transition organometallic complexes as reagents for the synthesis of complex organic mole...
In an effort to make diverse molecular complexity from simple hydrocarbons, tricarbonyl(cyclohexadie...
While (η5 -pentadienyl)iron(1+) cations were first prepared more than 40 years ago, the reactivity o...
The title compounds react with malonate anions by attack at both the substituted and unsubstituted t...
Alkynes add to tricarbony](vinytketene)iron(0) complexes to generate stable 1:1 adducts, the structu...