Dr. Jeffrey B Johnson MD
Doctor
2500 W Higgins Rd Suite 470 Schaumburg IL, 60195Rating
5/5
About
Dr. Jeffrey B Johnson MD is a top Doctor in Schaumburg, IL. With a passion for the field and an unwavering commitment to their specialty, Dr. Jeffrey B Johnson MD is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Dr. Jeffrey B Johnson MD is a prime example of a true leader in health care. As a leader and expert in their field, Dr. Jeffrey B Johnson MD is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In Schaumburg, IL, Dr. Jeffrey B Johnson MD is a true asset to their field and dedicated to the profession of medicine.
Education and Training
Loyola University Chicago Stritch School of Medicine 1967
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Kinetic isotope effect evidence for a concerted hydrogen transfer mechanism in transfer hydrogenations catalyzed by [p-(Me2CH)C6H4Me]Ru- (NHCHPhCHPhNSO2C6H4-p-CH3).
- Mechanism of ruthenium-catalyzed hydrogen transfer reactions. Concerted transfer of OH and CH hydrogens from an alcohol to a (Cyclopentadienone)ruthenium complex.
- Isomerization and deuterium scrambling evidence for a change in the rate-limiting step during imine hydrogenation by Shvo's hydroxycyclopentadienyl ruthenium hydride.
- Hydrogen elimination from a hydroxycyclopentadienyl ruthenium(II) hydride: study of hydrogen activation in a ligand-metal bifunctional hydrogenation catalyst.
- Selective substituent transfer from mixed zinc reagents in Ni-catalyzed anhydride alkylation.
- More than bystanders: the effect of olefins on transition-metal-catalyzed cross-coupling reactions.
- Spectroscopic determination of hydrogenation rates and intermediates during carbonyl hydrogenation catalyzed by Shvo's hydroxycyclopentadienyl diruthenium hydride agrees with kinetic modeling based on independently measured rates of elementary reacti
- Enantioselective cross-coupling of anhydrides with organozinc reagents: the
- Nickel-catalyzed reductive carboxylation of styrenes using CO2.
- Long-period earthquakes and co-eruptive dome inflation seen with particle image velocimetry.
- Chain mechanism for exchange of D2 with a ruthenium hydride.
- Rhodium-catalyzed acylation with quinolinyl ketones: carbon-carbon single bond activation as the turnover-limiting step of catalysis.
- Nickel-mediated decarbonylative cross-coupling of phthalimides with in situ generated diorganozinc reagents.
- Rate-limiting step of the Rh-catalyzed carboacylation of alkenes: C-C bond
- Steric and electronic effects influencing β-aryl elimination in the Pd-catalyzed carbon-carbon single bond activation of triarylmethanols.
Treatments
- Pregnancy
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