Skip to main content

Richard Nagorski

Professor, Organic Chemistry Associate Chair of Graduate Programs
Office
SLB Science Laboratory Building 205
Office Hours
Tues. 11-12 p.m. & Thurs. 9-10 a.m. or by appointment
  • About
  • Education
  • Awards & Honors
  • Selected Research

Research Interests & Areas

Areas of Current Research Interest The area of general interest within our group is the mechanisms and rate constants of reaction of biologically important molecules in water. In general, we prefer to observe the reaction of simple molecular analogs of the biological molecules of interest and extend our observations to the more complex biological molecules as our understanding of the system increases. There are two areas of current interest within the group. The first is the investigation of the stability constants and specifically, the mechanism of breakdown of carbinolamides. The general structure of carbinolamides is as shown in Scheme 1, and allows for great diversity of groups given the three possible positions of substitution. We are interested in these compounds because it has been shown that carbinolamides are intermediates in the enzyme mediated synthesis of a-amidated peptides. However, very little systematic work on the reaction of carbinolamides has been completed and even less is known about methods to catalyze the breakdown of these compounds. We propose the study of the reaction of various carbinolamides under aqueous conditions and the factors that catalyze their breakdown. The second area of current interest is the electrophilicity of amides, that is, how susceptible are amides to nucleophilic attack by a carbanion. Shown in Scheme 2 is the general reaction in which we are interested. The reaction proceeds by the formation of an enolate which can then nucleophilically attack the amide to form 2. Compound 2 will then undergo breakdown to form products. There are many interesting aspects to this reaction, the first of which is the reaction itself. We are familiar with similar reactions of this type (eg. Aldol, Claisen, Dieckmann) but this particular reaction has itself received little or no attention. Secondly, by investigating this reaction we will generate data that will allow us to make conclusions about the electrophilicity of amides that may eventually allow a better understanding of resonance. We propose the study of the mixed-Claisen condensation reaction above to determine the nature of this reaction and gain insight into the electrophilicity of amides. In addition, by changing the R groups on nitrogen we may be able to measure changes in the electrophilicity of the amide. Skills and Techniques of Importance: Students (undergraduate and graduate) who work in my labs will receive a variety of experiences: synthesis and purification of organic compounds learn the proper techniques for the determination and analysis of kinetic data and then put these techniques to use learn the operation of analytical instrumentation for the purposes of isolation and identification of reaction products spectral identification of organic compounds and become familiar with methods of obtaining said spectra

Ph D Organic Chemistry

University of Alberta
Edmonton, AB, Canada

BS Science

Brandon University
Brandon, MB, Canada

NSERC Post-Graduate Scholarship

1989

University of Alberta Graduate Faculty Fellowship

1989

NSERC Post-Graduate Scholarship

1988

University of Alberta Graduate Faculty Fellowship

1988

Grants and Contracts

Carbinolamides and N-(Hydroxybenzyl)urea Derivatives: Structure/Reactivity Correlations and Catalysis of the Aqueous Reaction
Richard Nagorski.
National Science Foundation. July 2005 - July 2011
Ring Strain and Antiaromaticity: Their Effect on the Generation and Reactivity of Enolates in Small-Ringed Ketones
Richard Nagorski.
American Chemical Society-Petroleum Research Fund, Type B. May 1 2004 - August 31 2008
Determination of the pKa of Benzocyclobutenone
Richard Nagorski.
Summer Faculty Fellowship (Illinois State University). July 1 2002 - June 30 2003
Metal-Ion and General Buffer Catalysis of the Aqueous Reaction of N- (Hydroxymethyl)benzamide as a Model for Enzymatic Catalysis
Richard Nagorski.
Research Cooporation. May 15 2002 - May 14 2004
Carbinolamides: Reaction and Catalytic Studies in Water
Richard Nagorski.
Pre-tenure Faculty Initiative Grant (Illinois State University). 2001 - 2002
Structure/Reactivity Correlations and Catalysis of the Aqueous Reaction of N-(Hydroxybenzyl) Carbinolamides
Richard Nagorski.
American Chemical Society-Petroleum Research Fund. September 1 2001 - August 31 2004
Carbinolamides: Structure/Reactivity Relationships in an Aqueous Environment
Richard Nagorski.
Research Corporation. May 2000 - May 2002

Journal Article

Determination of the pKa of Cyclobutanone: Bronsted Correlation of the General-Base Catalyzed Enolization in Aqueous Solution and the Effect of Ring-Strain
Steven M. Cope, Dishant Tailor, Richard Nagorski.
J. Org. Chem., 76, 380-390, (2011)
Solvent-free synthesis of monoacylaminals from the reaction of amides and aminals as precursors in carbinolamide synthesis
Matthew F. Sansone, Takaoki Koyanagi, David E. Przybyla, Richard Nagorski.
Tetrahedron Lett., 51, 6031-6033, (2010)
Rapid Amidic Hydrolysis: A Competitive Reaction Pathway Under Basic Conditions for N- (Hydroxymethyl)benzamide Derivatives Bearing Electron-Donating Groups
John L. Murphy, William J. Tenn III, Joseph J. Labuda, Richard Nagorski.
Tetrahedron Lett., 50, 7358-7361, (2009)
Rate of Formation of N-(Hydroxymethyl)benzamide Derivatives in Water as a Function of pH and Their Equilibrium Constants
Ramana V. Ankem, John L. Murphy, Richard Nagorski.
Tetrahedron Lett., 49, 6547-6549, (2008)
Amidates as Leaving Groups: Structure/Reactivity Correlation of the Hydroxide Dependent E1cB-Like Breakdown of Carbinolamides in Aqueous Solution
William J. Tenn III, John L. Murphy, Jessica K. Bim-Merle, Jason A. Brown, Adam J. Junia, Malea A. Price, Richard Nagorski.
J. Org. Chem., 72, 6075-6083, (2007)
General-Buffer Catalysis of the Reaction of N-(Hydroxymethyl)benzamide: A New Pathway for the Aqueous Reaction of Carbinolamides
A. G. Mennenga, A. L. Johnson, Richard Nagorski.
Tetrahedron Lett., 46, 3079-3083, (2005)
Ring Strain and Its Effect on the Rate of the General-Base Catalyzed Enolization of Cyclobutanone
R. J. Cantlin, J. Drake, Richard Nagorski.
Org. Lett., 4, 2433-2436, (2002)
The Reversible Formation of the Enolate of Benzocyclobutenone Under Aqueous Conditions
A. D. DeAtley, K. M. Broadus, Richard Nagorski.
J.Am.Chem.Soc., 123, 8428-8429, (2002)
Effect of Electron Withdrawing Groups on the Aqueous Reaction of N- (Hydroxymethyl)benzamide Derivatives
W. J. Tenn III, N. L. French, Richard Nagorski.
Org. Lett., 3, 75-78, (2001)
Mechanistic Imperatives for Aldose-Ketose Isomerization in Water: Specific, General Base and Metal Ion Catalyzed Isomerization of Glyceraldehyde with Proton and Hydride Transfer
Richard Nagorski, J. P. Richard.
J. Am. Chem. Soc., 123, 794-802, (2001)
The Reversible Formation of the Enolate of Benzocyclobutenone Under Aqueous Conditions
Richard Nagorski, A. D. DeAtley, K. M. Broadus.
J. Am. Chem. Soc., 123, 8428-8429, (2001)
Mechanistic Imperatives for Catalysis of Aldol Addition Reactions: Partitioning of the Enolate Intermediate Between Reaction with Bronsted Acids and the Carbonyl Group
Richard Nagorski, J. P. Richard.
J. Am. Chem. Soc., 121, 4763-4770, (1999)
Imperatives for Enzymatic Catalysis of Isomerization of Sugars and Sugar Phosphates
J. P. Richard, J. Crugeiras, Richard Nagorski.
J. Phys. Org. Chem., 11, 512-518, (1998)
Mechanistic Imperatives for Enzymatic Catalysis of Aldose-Ketose Isomerization: Isomerization of Glyceraldehyde in Weakly Alkaline Aqueous Solution with Intramolecular Transfer of a Hydride Ion
Richard Nagorski, J. P. Richard.
J. Am. Chem. Soc., 118, 7432-7433, (1996)
Absolute and Relative Electrophilicities of a Carbonyl Group and Tertiary Ammonium Ions toward a Simple Enolate Ion
Richard Nagorski, T. Mizerski, J. P. Richard.
J. Am. Chem. Soc., 117, 4718-4719, (1995)
Electrophilic Bromination of 7-Norbornylidene-7-Norborane. The Observation of An Unusually Large Inverse Deuterium Kinetic Isotope Effect
H. Slebocka-Tilk, S. Motellebi, Richard Nagorski, P. Turner, R. S. Brown, R. McDonald.
J. Am. Chem. Soc., 117, 8769-8776, (1995)
The Nucleofugality and Nucleophilicity of the Benzotriazole Group in Solvolysis
J. P. Richard, Richard Nagorski, S. Rudich, T. L. Amyes, A. R. Katritzky, A. P. Wells.
J. Org. Chem., 60, 5989-5991, (1995)
Observation of an Unusually Large Inverse Secondary Isotope Effect for the Reaction of a Sterically Congested Olefin with Br2
Richard Nagorski, H. Slebocka-Tilk, R. S. Brown.
J. Am. Chem. Soc., 116, 419-420, (1994)
Stable Bromonium and Iodonium Ions of the Hindered Olefins Adamantylideneadamantane and Bicyclo[3.3.1]nonane. X-Ray Structure, Transfer of Positive Halogens to Acceptor Olefins, and ab Intio Studies
R. S. Brown, Richard Nagorski, A. J. Bennet, R.E.D. McClung, G.H.M. Aarts, M. Klowbukowski, R. McDonald, B. D. Santarsiero.
J. Am. Chem. Soc., 116, 2448-2456, (1994)
Reversible Formation of Bromonium Ions. The Bromonium Ion Produced from the Solvolysis of the trans-2-Bromotriflate of Cyclohexane in MeOH or HOAc Containing Added Bromide Preferentially Reacts with Br- on Br+
C. Y. Zheng, H. Slebocka-Tilk, Richard Nagorski, L. Alvardo, R. S. Brown.
J. Org. Chem., 58, 2122-2127, (1993)
Electrophilic Addition of Br2 to Olefins in the Presence of Nucleophilic Trapping Anions. Implications for the Lifetimes of Bromonium Ion Intermediates Produced from Electrophilic Bromination of Olefins in Methanol
Richard Nagorski, R. S. Brown.
J. Am. Chem. Soc., 114, 7773-7779, (1992)

Presentations

N-(Hydroxybenzyl)benzamides: pH-Rate Profiles and Zn2+ Catalysis of their Breakdown in H2O
P. M. Siena, T. Koyanagi, Richard Nagorski.
42nd Meeting of the American Chemical Society Central Region, Indiana University-Purdue University Indianapolis, IN, June 5, 2011
Non-linear Hammett Correlation for the Hydroxide-Dependent Breakdown of Aromatic Substituted N-(Hydroxybenzyl)acetamides
Richard Nagorski.
42nd Meeting of the American Chemical Society Central Region, Indiana University-Purdue University Indianapolis, IN, June 5, 2011
Synthesis of N-(-Alkoxybenzyl)amide Derivatives and Initial pH-Dependent Rate Studies in H2O
S. C. Stewart, Richard Nagorski.
42nd Meeting of the American Chemical Society Central Region, Indiana University-Purdue University Indianapolis, IN, June 5, 2011
-Hydroxyhippuric Acid Derivatives: pH-Dependent Aqueous Kinetics and Buffer Catalysis
K. Feken, J. A. Brown, L. N. Skelton, Richard Nagorski.
42nd Meeting of the American Chemical Society Central Region, Indiana University-Purdue University Indianapolis, IN, June 5, 2011
The Synthesis and Characterization of N-(- Alkoxybenzyl)acetamides
S. Stewart, Richard Nagorski.
Illinois State University Undergraduate Research Symposium, Normal, IL, March 25, 2011
The Synthesis and Characterization of N-(Alkoxybenzyl)acetamide Derivatives
S. Schauff, Richard Nagorski.
Illinois State University Undergraduate Research Symposium, Normal, IL, April 16, 2010
N-(Hydroxybenzyl)benzamide Derivatives: Hydroxide- Dependent Breakdown and Correlation to the pH-Rate Profiles
P. Siena, T. Koyanagi, Richard Nagorski.
Illinois State University Research Symposium, Normal, IL, March 26, 2010
Ring Strain and Its Effect on the Rate of Enolization of Strained and Unstrained Cyclic Ketones and the Correlation of the Brønsted - value to the Ring Size
D. Tailor, B. E. Blank, R. S. Yarbrough, Richard Nagorski.
Illinois State University Research Symposium, Normal, IL, March 26, 2010
The Synthesis and Characterization of N- (Alkoxybenzyl)acetamide Derivatives
S. C. Schauff, Richard Nagorski.
Illinois State University Chemistry Club Spring Research Symposium, Normal, IL, March 23, 2010
Comparison of Enolization Rates of Strained and Unstrained Cyclic Ketones to 3-Pentanone
D. Tailor, B. E. Bank, R. S. Yarbrough, Richard Nagorski.
Department of Chemistry Research Symposium, Normal, IL, , 2009
Comparison of Enolization Rates of Strained and Unstrained Cyclic Ketones to 3-Pentanone
D. Tailor, B. E. Blank, R. S. Yarbrough, Richard Nagorski.
Graduate Research Symposium, Normal, IL, , 2009
Synthesis of N-(Hydroxy-4-(trifluoromethyl)benzyl)acetamide and Initial Kinetic Studies
K. M. Reschak, Richard Nagorski.
Undergraduate Research Symposium, Normal, IL, , 2009
The Synthesis and Characterization of N- (Alkoxybenzyl)acetamide Derivatives
S. C. Schauff, Richard Nagorski.
Undergraduate Research Symposium, Normal, IL, , 2009
Amidic Hydrolysis: A Competitive Reaction for the Breakdown of Some N- (Hydroxymethyl)benzamide Derivatives Under Basic Conditions
Richard Nagorski.
37th Ontario-Quebec Physical Organic Mini-Symposium, Buffalo, NY, November 15, 2009
Enolization Rates of Cyclic Ketones and the Apparent Insensitivity of the Bronsted Beta-Value to Ring Size
Dishant Tailor, Richard Nagorski.
37th Ontario-Quebec Physical Organic Mini-Symposium, Buffalo, NY, November 15, 2009
The Synthesis and Characterization of N- (Alkoxybenzyl)acetamide Derivatives
S. C. Schauff, Richard Nagorski.
Illinois Heartland Local Section of the American Chemical Society 2009 Student Poster Session, ISU-Normal, IL, September 21, 2009
Carbinolamides: A New Competing Hydrolytic Mechanism Leading to a Nonlinear Hammett Correlation for the Hydroxide-Dependent Breakdown
Richard Nagorski.
238th ACS National Meeting, Washington, D.C., August 20, 2009
Enolization Rates of Strained and Unstrained Cyclic Ketones and 3- Pentanone: Trends and Predicted pKa’s
Dishant Tailor, Richard Nagorski.
238th ACS National Meeting, Washington, D.C., August 20, 2009
Comparison of Enolization Rates of Strained and Unstrained Cyclic Ketones to 3-Pentanone
Dishant Tailor, B. E. Blank, R. S. Yarbrough, Richard Nagorski.
38th Great Lakes Regional ACS Meeting, Lincolnshire Marriott Resort, Lincolnshire, IL, May 13, 2009
Nonlinear Hammett Correlation for the Hydroxide-Dependent Reaction of Carbinolamides: Amide Hydrolysis?
John L. Murphy, Jr., William J. Tenn III, Joseph J. Labuda, Richard Nagorski.
38th Great Lakes Regional ACS Meeting, Lincolnshire Marriott Resort, Lincolnshire, IL, May 13, 2009
Progress towards the synthesis of 2-(2’-oxopropyl)-N,Ndimethylbenzamide
B. M. Knight, Richard Nagorski.
ACS-SEED Student Symposium, ISU-Normal, IL, July, 2008
Determination of the pKa of alpha-Hydrogens in cyclohexanone by deuterium incorporation studies
B. E. Blank, S. M. Cope, Richard Nagorski.
Undergraduate Research Symposium, Normal, IL, , 2007
Solvent-free synthesis of monoacylaminals and hydrolysis to form carbinolamides
T. Koyanagi, Richard Nagorski.
Undergraduate Research Symposium, Normal, IL, , 2007
Organic Synthesis during the Summer of 2007
E. Williams, Richard Nagorski.
ACS-SEED Student Symposium, ISU-Normal, IL, July, 2007
N-(Hydroxymethyl)benzamides: Rates of Formation as a Function of pH and Equilibrium Constants in Water
Richard Nagorski, R. V. Ankem.
2007 Gordon Research Conference on Physical Organic Chemistry, Holderness, NH, June 29, 2007