Jeremy T Starr

发表

Binding site elucidation and structure guided design of macrocyclic IL-17A antagonists

Li Xing, Guoyun Bai, Atli Thorarensen, 2016, Scientific Reports.

Scalable, Electrochemical Oxidation of Unactivated C–H Bonds

Phil S Baran, Jinshan Chen, P. Baran, 2017, Journal of the American Chemical Society.

Electrochemically Enabled, Nickel-Catalyzed Amination.

Julien C. Vantourout, Ming Yan, P. Baran, 2017, Angewandte Chemie.

Novel monobactams utilizing a siderophore uptake mechanism for the treatment of gram-negative infections.

V. Shanmugasundaram, M. Huband, T. Harris, 2012, Bioorganic & medicinal chemistry letters.

Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications.

David P. Hickey, Julien C. Vantourout, N. Sach, 2019, Journal of the American Chemical Society.

Hydropyridylation of Olefins by Intramolecular Minisci Reaction.

S. Bordi, Jeremy T Starr, 2017, Organic letters.

Process Development for the Synthesis of Monocyclic β-Lactam Core 17

Jeremy T Starr, Matthew F Brown, M. Lall, 2018 .

One-pot synthesis of N-arylpyrazoles from arylhalides.

Jeremy T Starr, Mark R. Rauckhorst, Brian S. Gerstenberger, 2009, Organic letters.

The synthesis and biological evaluation of novel series of nitrile-containing fluoroquinolones as antibacterial agents.

W. Denny, S. Hagen, J. Smaill, 2007, Bioorganic & medicinal chemistry letters.

One-pot oxidation and rearrangement of propargylamines and in situ pyrazole synthesis.

J. Chen, Jennifer A Young, Jeremy T Starr, 2014, Organic letters.

Pyridone-conjugated monobactam antibiotics with gram-negative activity.

V. Shanmugasundaram, M. Huband, T. Harris, 2013, Journal of medicinal chemistry.

Synthesis of PEG-Functionalized Amines Using Ruthenium-Catalyzed Hydrogen Borrowing.

Jennifer A Young, Jeremy T Starr, Daniel P. Uccello, 2020, Organic letters.

An Improved Oxidation Method for the Synthesis of Azodicarbonyl Compounds

Jeremy T Starr, B. McNelis, H. Dang, 1997 .

Enantioselective Synthesis of the Cyclopentyl Core of the Axinellamines

E. Carreira, G. Koch, Jeremy T Starr, 2000 .

5-(2-Pyrimidinyl)-imidazo[1,2-a]pyridines are antibacterial agents targeting the ATPase domains of DNA gyrase and topoisomerase IV.

R. M. Owen, M. Huband, Huifen Chen, 2009, Bioorganic & medicinal chemistry letters.

A cycloaddition cascade approach to the total synthesis of (-)-FR182877.

Davidr . Evans, Jeremy T Starr, D. A. Evans, 2003, Journal of the American Chemical Society.

A cascade cycloaddition strategy leading to the total synthesis of (-)-FR182877.

Davidr . Evans, Jeremy T Starr, D. A. Evans, 2002, Angewandte Chemie.

Siderophore receptor-mediated uptake of lactivicin analogues in gram-negative bacteria.

V. Shanmugasundaram, M. Huband, Ye Che, 2014, Journal of medicinal chemistry.

Nucleophilic additions to a spiro[2,4]hepta-4,6-diene 4-nitrile: Synthesis of 1,2-disubstituted cyclopentenes

E. Carreira, Jeremy T Starr, A. Baudat, 1998 .

Delineating the role of cooperativity in the design of potent PROTACs for BTK

Graham M. West, James Smith, V. Shanmugasundaram, 2018, Proceedings of the National Academy of Sciences.

Late Stage Lead Diversification (LSLD) Coupled with Quantitative NMR Spectroscopy to Identify New SAR Vectors at Nanomole Scale Synthesis: Application to Loratadine a Human Histamine H1 Receptor Inverse Agonist.

G. S. Walker, R. Obach, N. Sach, 2020, Journal of medicinal chemistry.

Structure guided development of novel thymidine mimetics targeting Pseudomonas aeruginosa thymidylate kinase: from hit to lead generation.

W. Roush, Jeremy T Starr, J. Choi, 2012, Journal of medicinal chemistry.

Intrinsic reactivity profile of electrophilic moieties to guide covalent drug design: N-α-acetyl-L-lysine as an amine nucleophile

R. Obach, A. Gilbert, M. Flanagan, 2016 .

Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitors.

G. S. Walker, V. Shanmugasundaram, R. Obach, 2014, Journal of medicinal chemistry.

Discovery of Dap-3 polymyxin analogues for the treatment of multidrug-resistant Gram-negative nosocomial infections.

Bryan M. Li, A. Stepan, J. Aubrecht, 2013, Journal of medicinal chemistry.

Discovery of a Selective Covalent Inhibitor of Lysophospholipase-like 1 (LYPLAL1) as a Tool to Evaluate the Role of this Serine Hydrolase in Metabolism.

K. Fennell, J. Pandit, K. Parris, 2016, ACS chemical biology.

Chemical and computational methods for the characterization of covalent reactive groups for the prospective design of irreversible inhibitors.

G. S. Walker, V. Shanmugasundaram, M. Hayward, 2014, Journal of medicinal chemistry.

Novel Methods for Prioritizing "Close-In" Analogs from Structure-Activity Relationship Matrices

Christopher S. Poss, V. Shanmugasundaram, Kjell Johnson, 2017, J. Chem. Inf. Model..

Electrochemically Enabled, Nickel-Catalyzed Amination.

Julien C. Vantourout, Ming Yan, P. Baran, 2017, Angewandte Chemie.