Activation of carbonhydrogen bonds by metal complexes: Mechanistic, kinetic and thermodynamic considerations
Reference (65)
Adv. Organomet. Chem.
(1977)- et al.
Coord. Chem. Rev.
(1977) J. Organomet. Chem.
(1972)J. Catal.
(1962)- et al.
Inorg. Chim. Acta
(1983) Adv. Chem. Ser.
(1966)Discuss. Faraday Soc.
(1968)Acc. Chem. Res.
(1975)Catalysis
(1977)Pure Appl. Chem.
(1978)
Science
J. Am. Chem. Soc.
J. Am. Chem. Soc.
Organometallics
J. Am. Chem. Soc.
J. Am. Chem. Soc.
J. Am. Chem. Soc.
Organometallics
J. Am. Chem. Soc.
Chemtech
Organometallics
J. Chem. Soc., Chem. Commun.
J. Chem. Soc., Chem. Commun.
J. Chem. Soc., Chem. Commun.
J. Chem. Soc., Chem. Commun.
Acc. Chem. Res.
Annu. Rev. Phys. Chem.
Acc. Chem. Res.
Acc. Chem. Res.
Pure Appl. Chem.
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