2000 - Fellow of Alfred P. Sloan Foundation
K. A. Woerpel mostly deals with Stereochemistry, Oxocarbenium, Nucleophilic substitution, Stereoselectivity and Organic chemistry. His biological study spans a wide range of topics, including Suzuki reaction, Palladium, Stille reaction, Computational chemistry and Nucleophile. His studies deal with areas such as Substituent, Steric effects, Alkoxy group and Ring as well as Oxocarbenium.
In his work, Heteroatom is strongly intertwined with Conformational isomerism, which is a subfield of Substituent. His Nucleophilic substitution study is concerned with Medicinal chemistry in general. The concepts of his Stereoselectivity study are interwoven with issues in Diol, Organic reaction, Stereospecificity and Lithium.
Organic chemistry, Medicinal chemistry, Catalysis, Stereochemistry and Stereoselectivity are his primary areas of study. The various areas that K. A. Woerpel examines in his Medicinal chemistry study include Oxonium ion, Ring, Photochemistry, Reactivity and Nucleophile. He has researched Catalysis in several fields, including Metal, Polymer chemistry and Silylene.
His study in Stereochemistry is interdisciplinary in nature, drawing from both Nucleophilic substitution, Stereocenter, Lewis acids and bases and Oxocarbenium. His work is dedicated to discovering how Oxocarbenium, Substituent are connected with Alkoxy group and other disciplines. His Stereoselectivity research includes themes of Formamides and Organic synthesis.
His primary areas of study are Medicinal chemistry, Ring, Catalysis, Reactivity and Reagent. His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Group, Adduct, Allylic rearrangement and Diastereomer. His Ring research incorporates themes from Stereochemistry, Nucleophile and Concerted reaction.
K. A. Woerpel studies Nucleophile, focusing on Oxocarbenium in particular. His Catalysis research integrates issues from Cobalt and Photochemistry. His Alkyl study is concerned with the larger field of Organic chemistry.
His main research concerns Oxidative stress, Cancer cell, Reactivity, Medicinal chemistry and Ring. His Oxidative stress study combines topics from a wide range of disciplines, such as Apoptosis, Programmed cell death and Cell biology. K. A. Woerpel focuses mostly in the field of Reactivity, narrowing it down to matters related to Cycloaddition and, in some cases, Photochemistry, Ring strain, Cycloheptene and Nucleophile.
His Medicinal chemistry research includes elements of Hydroboration, Alkene and Halide. His study in Stereochemistry extends to Ring with its themes. K. A. Woerpel does research in Stereochemistry, focusing on Steric effects specifically.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease
Brent R. Stockwell;José Pedro Friedmann Angeli;Hülya Bayir;Ashley I. Bush.
Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins
David A. Evans;Keith A. Woerpel;Mira M. Hinman;Margaret M. Faul.
Journal of the American Chemical Society (1991)
Stereochemistry of Nucleophilic Substitution Reactions Depending upon Substituent: Evidence for Electrostatic Stabilization of Pseudoaxial Conformers of Oxocarbenium Ions by Heteroatom Substituents
Leticia Ayala;Claudia G Lucero;Jan Antoinette C Romero;Sarah A Tabacco.
Journal of the American Chemical Society (2003)
FINO2 initiates ferroptosis through GPX4 inactivation and iron oxidation.
Michael M. Gaschler;Alexander A. Andia;Hengrui Liu;Joleen M. Csuka.
Nature Chemical Biology (2018)
A Stereoelectronic Model To Explain the Highly Stereoselective Reactions of Nucleophiles with Five-Membered-Ring Oxocarbenium Ions
Catharine H. Larsen;Brian H. Ridgway;Jared T. Shaw;K. A. Woerpel.
Journal of the American Chemical Society (1999)
Stereochemical Reversal of Nucleophilic Substitution Reactions Depending upon Substituent: Reactions of Heteroatom-Substituted Six-Membered-Ring Oxocarbenium Ions through Pseudoaxial Conformers
Jan Antoinette C. Romero;Sarah A. Tabacco;K. A. Woerpel.
Journal of the American Chemical Society (2000)
‘Bis(oxazolines)’ as Ligands for Self‐Assembling Chiral Coordination Polymers— Structure of a Copper(I) Catalyst for the Enantioselective Cyclopropanation of Olefins
David A. Evans;Keith A. Woerpel;Michael J. Scott.
Angewandte Chemie (1992)
Stereoselective C-Glycosylation Reactions of Ribose Derivatives: Electronic Effects of Five-Membered Ring Oxocarbenium Ions
Catharine H. Larsen;Brian H. Ridgway;Jared T. Shaw;Deborah M. Smith.
Journal of the American Chemical Society (2005)
An Improved Procedure for the Preparation of 2,2-Bis[2-[4(S)- tert-butyl-1,3-oxazolinyl]]propane [(S,S)-tert-Butylbis(oxazoline)] and Derived Copper(II) Complexes
David A. Evans;Gretchen S. Peterson;Jeffrey S. Johnson;David M. Barnes.
Journal of Organic Chemistry (1998)
Stereoselective C-glycosylation reactions of pyranoses: the conformational preference and reactions of the mannosyl cation.
Claudia G. Lucero;K. A. Woerpel.
Journal of Organic Chemistry (2006)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: