R. W. Nagorski

发表

Absolute and relative electrophilicities of a carbonyl group and tertiary ammonium ions toward a simple enolate ion

John P. Richard, R. W. Nagorski, Tadeusz Mizerski, 1995 .

IMPERATIVES FOR ENZYMATIC CATALYSIS OF ISOMERIZATION OF SUGARS AND SUGAR PHOSPHATES

R. W. Nagorski, J. Richard, J. Crugeiras, 1998 .

Carbinol Derivatives of N ‐(α‐Hydroxybenzyl)benzamide: Acid and Base‐Dependent Kinetics in Water and the Mechanistic Implications for Carbinolamide Reactivity

R. W. Nagorski, K. S. Tyminski, Sarah C. Stewart, 2021, ChemistrySelect.

Observation of an unusually large inverse secondary deuterium kinetic isotope effect for the reaction of a sterically congested olefin with bromine

R. W. Nagorski, R. S. Brown, H. Ślebocka-tilk, 1994 .

N-(Hydroxybenzyl)benzamide Derivatives: Aqueous pH-Dependent Kinetics and Mechanistic Implications for the Aqueous Reactivity of Carbinolamides.

R. W. Nagorski, Takaoki Koyanagi, David E. Przybyla, 2019, The Journal of organic chemistry.

Solvent-free synthesis of monoacylaminals from the reaction of amides and aminals as precursors in carbinolamide synthesis

R. W. Nagorski, Takaoki Koyanagi, David E. Przybyla, 2010 .

Rapid amidic hydrolysis: a competitive reaction pathway under basic conditions for N-(hydroxymethyl)benzamide derivatives bearing electron-donating groups

John L. Murphy, R. W. Nagorski, W. Tenn, 2009 .

Rate of formation of N-(hydroxymethyl)benzamide derivatives in water as a function of pH and their equilibrium constants

John L. Murphy, R. W. Nagorski, Ramana V. Ankem, 2008 .

Kinetic dependence of the aqueous reaction of N-(hydroxymethyl)benzamide derivatives upon addition of electron-withdrawing groups.

R. W. Nagorski, W. Tenn, N. French, 2001, Organic letters.

Mechanistic Imperatives for Catalysis of Aldol Addition Reactions: Partitioning of the Enolate Intermediate between Reaction with Brønsted Acids and the Carbonyl Group

R. W. Nagorski, J. Richard, 1999 .

General-buffer catalysis of the reaction of N-(hydroxymethyl)benzamide: a new pathway for the aqueous reaction of carbinolamides

R. W. Nagorski, Amanda G. Mennenga, Amy L. Johnson, 2005 .

Ring strain and its effect on the rate of the general-base catalyzed enolization of cyclobutanone.

R. W. Nagorski, Ryan J Cantlin, J. Drake, 2002, Organic letters.

Stable Bromonium and Iodonium Ions of the Hindered Olefins Adamantylideneadamantane and Bicyclo[3.3.1]nonylidenebicyclo[3.3.1]nonane. X-Ray Structure, Transfer of Positive Halogens to Acceptor Olefins, and ab Initio Studies

R. W. Nagorski, B. Santarsiero, A. J. Bennet, 1994 .

Reversible formation of bromonium ions. Preferential reaction of Br- on the Br+ of the bromonium ion produced from the solvolysis of trans-2-bromocyclohexyl triflate in methanol or acetic acid containing added bromide

R. W. Nagorski, L. Alvarado, R. S. Brown, 1993 .

Mechanistic imperatives for aldose-ketose isomerization in water: specific, general base- and metal ion-catalyzed isomerization of glyceraldehyde with proton and hydride transfer.

R. W. Nagorski, J. Richard, R. Nagorski, 2001, Journal of the American Chemical Society.

Electrophilic Bromination of 7-Norbornylidene-7'-Norbornane. The Observation of an Unusually Large Inverse Deuterium Kinetic Isotope Effect

R. W. Nagorski, R. Mcdonald, R. S. Brown, 1995 .

Mechanistic Imperatives for Enzymatic Catalysis of Aldose−Ketose Isomerization: Isomerization of Glyceraldehyde in Weakly Alkaline Aqueous Solution Occurs with Intramolecular Transfer of a Hydride Ion

R. W. Nagorski, J. Richard, 1996 .

Phosphodianion Activation of Enzymes for Catalysis of Central Metabolic Reactions

R. W. Nagorski, J. Richard, T. L. Amyes, 2021, Journal of the American Chemical Society.