Year |
Citation |
Score |
2024 |
Sahu S, Emenike B, Beusch CM, Bagchi P, Gordon DE, Raj M. Copper(I)-nitrene platform for chemoproteomic profiling of methionine. Nature Communications. 15: 4243. PMID 38762540 DOI: 10.1038/s41467-024-48403-0 |
0.301 |
|
2024 |
Emenike B, Czabala P, Farhi J, Swaminathan J, Anslyn EV, Spangle J, Raj M. Tertiary Amine Coupling by Oxidation for Selective Labeling of Dimethyl Lysine Post-Translational Modifications. Journal of the American Chemical Society. 146: 10621-10631. PMID 38584362 DOI: 10.1021/jacs.4c00253 |
0.371 |
|
2024 |
Wills R, Shirke R, Hrncir H, Talbott JM, Sad K, Spangle JM, Gracz AD, Raj M. Tunable fluorescent probes for detecting aldehydes in living systems. Chemical Science. 15: 4763-4769. PMID 38550703 DOI: 10.1039/d4sc00391h |
0.728 |
|
2024 |
Emenike B, Shahin S, Raj M. Bioinspired Synthesis of Allysine for Late-Stage Functionalization of Peptides. Angewandte Chemie (International Ed. in English). e202403215. PMID 38529755 DOI: 10.1002/anie.202403215 |
0.842 |
|
2024 |
Bruce A, Adebomi V, Czabala P, Palmer J, Bhardwaj G, Raj M, McFadden WM, Lorson ZC, Slack RL, Sarafianos SG. A Tag-Free Platform for Synthesis and Screening of Cyclic Peptide Libraries. Angewandte Chemie (International Ed. in English). e202320045. PMID 38529717 DOI: 10.1002/anie.202320045 |
0.719 |
|
2023 |
Prosser LC, Talbott JM, Garrity RP, Raj M. Correction to "C-Terminal Arginine-Selective Cleavage of Peptides as a Method for Mimicking Carboxypeptidase B". Organic Letters. 25: 7457-7458. PMID 37791669 DOI: 10.1021/acs.orglett.3c02915 |
0.827 |
|
2023 |
Brimble MA, Ackermann L, Li YM, Raj M. Chemoselective Methods for Labeling and Modification of Peptides and Proteins. Organic Letters. 25: 6605-6606. PMID 37711046 DOI: 10.1021/acs.orglett.3c02630 |
0.551 |
|
2023 |
Prosser LC, Talbott JM, Garrity RP, Raj M. C-Terminal Arginine-Selective Cleavage of Peptides as a Method for Mimicking Carboxypeptidase B. Organic Letters. 25: 6206-6210. PMID 37585337 DOI: 10.1021/acs.orglett.3c02418 |
0.834 |
|
2023 |
Wills R, Farhi J, Czabala P, Shahin S, M Spangle J, Raj M. Chemical sensors for imaging total cellular aliphatic aldehydes in live cells. Chemical Science. 14: 8305-8314. PMID 37564401 DOI: 10.1039/d3sc02025h |
0.763 |
|
2023 |
Emenike B, Donovan J, Raj M. Multicomponent Oxidative Nitrile Thiazolidination Reaction for Selective Modification of N-terminal Dimethylation Posttranslational Modification. Journal of the American Chemical Society. 145: 16417-16428. PMID 37486086 DOI: 10.1021/jacs.3c02369 |
0.406 |
|
2023 |
Shao H, Adebomi V, Bruce A, Raj M, Houk KN. Intramolecular Hydrogen Bonding Enables a Zwitterionic Mechanism for Macrocyclic Peptide Formation: Computational Mechanistic Studies of CyClick Chemistry. Angewandte Chemie (International Ed. in English). e202307210. PMID 37475575 DOI: 10.1002/anie.202307210 |
0.844 |
|
2023 |
Wang Y, Czabala P, Raj M. Bioinspired one-pot furan-thiol-amine multicomponent reaction for making heterocycles and its applications. Nature Communications. 14: 4086. PMID 37429878 DOI: 10.1038/s41467-023-39708-7 |
0.546 |
|
2023 |
Negi RC, Machhan P, Raj M, Barwal VK, Chander S, Thakur S, Mokta J. Clinical Profile and Outcome of Snake Bite Patients from Tertiary Healthcare Center: In Sub-Himalayan Region: A Medical College-based Study. The Journal of the Association of Physicians of India. 71: 11-12. PMID 37355819 DOI: 10.5005/japi-11001-0228 |
0.195 |
|
2022 |
Wills R, Adebomi V, Spancake C, Cohen RD, Raj M. Synthesis of L-cyclic tetrapeptides by backbone amide activation CyClick strategy. Tetrahedron. 126. PMID 37994371 DOI: 10.1016/j.tet.2022.133071 |
0.833 |
|
2022 |
Adebomi V, Wang Y, Sriram M, Raj M. Selective Conversion of Unactivated C-N Amide Bond to C-C bond via Steric and Electronic Resonance Destabilization. Organic Letters. PMID 36067532 DOI: 10.1021/acs.orglett.2c02420 |
0.785 |
|
2022 |
Chen G, Raj M, Yudin A. Introduction to 'Synthesis and chemical biology of macrocycles'. Rsc Chemical Biology. 3: 993. PMID 35975002 DOI: 10.1039/d2cb90018a |
0.342 |
|
2022 |
Emenike B, Nwajiobi O, Raj M. Covalent Chemical Tools for Profiling Post-Translational Modifications. Frontiers in Chemistry. 10: 868773. PMID 35860626 DOI: 10.3389/fchem.2022.868773 |
0.802 |
|
2022 |
Nwajiobi O, Verma AK, Raj M. Rapid Arene Triazene Chemistry for Macrocyclization. Journal of the American Chemical Society. 144: 4633-4641. PMID 35232021 DOI: 10.1021/jacs.2c00464 |
0.861 |
|
2021 |
Tang KC, Maddox SM, Backus KM, Raj M. Tunable heteroaromatic azoline thioethers (HATs) for cysteine profiling. Chemical Science. 13: 763-774. PMID 35173941 DOI: 10.1039/d1sc04139h |
0.835 |
|
2021 |
McFadden WM, Snyder AA, Kirby KA, Tedbury PR, Raj M, Wang Z, Sarafianos SG. Rotten to the core: antivirals targeting the HIV-1 capsid core. Retrovirology. 18: 41. PMID 34937567 DOI: 10.1186/s12977-021-00583-z |
0.218 |
|
2021 |
Raj M, Tang KC, Cao J, Boatner LM, Li L, Farhi J, Houk KN, Spangle J, Backus KM. Tunable Amine-Reactive Electrophiles for Selective Profiling of Lysine. Angewandte Chemie (International Ed. in English). PMID 34762358 DOI: 10.1002/anie.202112107 |
0.391 |
|
2021 |
Adebomi V, Sriram M, Streety X, Raj M. Metal-Free Selective Modification of Secondary Amides: Application in Late-Stage Diversification of Peptides. Organic Letters. PMID 34251828 DOI: 10.1021/acs.orglett.1c01622 |
0.841 |
|
2020 |
Raj M, Nwajiobi O, Mahesh S, Streety X. Triazenation Unable Selective Reaction of Secondary Amines (TrUSS) for Tagging Monomethyl Lysine PTMs. Angewandte Chemie (International Ed. in English). PMID 33354813 DOI: 10.1002/anie.202013997 |
0.81 |
|
2020 |
Raj M, Tang KC. One Step Azolation strategy for site- and chemo-selective labeling of proteins with mass sensitive probes. Angewandte Chemie (International Ed. in English). PMID 33047860 DOI: 10.1002/anie.202007608 |
0.795 |
|
2020 |
Raj M, Wills R, Adebomi V. Site Selective Peptide Macrocyclization. Chembiochem : a European Journal of Chemical Biology. PMID 32794268 DOI: 10.1002/cbic.202000398 |
0.841 |
|
2020 |
Sim YE, Nwajiobi O, Mahesh S, Cohen RD, Reibarkh MY, Raj M. Secondary amine selective Petasis (SASP) bioconjugation. Chemical Science. 11: 53-61. PMID 32110356 DOI: 10.1039/C9Sc04697F |
0.825 |
|
2020 |
Wills RD, Adebomi VT, Raj M. Peptide Cyclization at High Concentration Synlett. DOI: 10.1055/S-0040-1707165 |
0.623 |
|
2019 |
Raj M, Mahesh S, Adebomi V, Muneeswaran Z. Bioinspired Nitroalkylation for Selective Protein Modification and Peptide Stapling. Angewandte Chemie (International Ed. in English). PMID 31774930 DOI: 10.1002/Anie.201908593 |
0.841 |
|
2019 |
Raj M, Cohen RD, Adebomi V, Wills R, Martin G, Chavers H. CyClick Chemistry for Synthesis of Cyclic Peptides. Angewandte Chemie (International Ed. in English). PMID 31617285 DOI: 10.1002/Anie.201911900 |
0.846 |
|
2018 |
Mahesh S, Tang KC, Raj M. Amide Bond Activation of Biological Molecules. Molecules (Basel, Switzerland). 23. PMID 30322008 DOI: 10.3390/Molecules23102615 |
0.823 |
|
2018 |
Howard TS, Cohen RD, Nwajiobi O, Muneeswaran ZP, Sim YE, Lahankar NN, Yeh JT, Raj M. Amino-Acid-Catalyzed Direct Aldol Bioconjugation. Organic Letters. PMID 30125118 DOI: 10.1021/Acs.Orglett.8B02265 |
0.732 |
|
2018 |
Elashal HE, Cohen RD, Elashal HE, Zong C, Link AJ, Raj M. Cyclic and Lasso Peptides: Sequence Determination, Topology Analysis, and Rotaxane Formation. Angewandte Chemie (International Ed. in English). PMID 29645322 DOI: 10.1002/Anie.201801299 |
0.846 |
|
2018 |
Elashal HE, Cohen RD, Elashal HE, Raj M. Oxazolidinone-Mediated Sequence Determination of One-Bead One-Compound Cyclic Peptide Libraries. Organic Letters. PMID 29617143 DOI: 10.1021/Acs.Orglett.8B00717 |
0.846 |
|
2018 |
Zong C, Cheung-Lee WL, Elashal HE, Raj M, Link AJ. Albusnodin: an acetylated lasso peptide from Streptomyces albus. Chemical Communications (Cambridge, England). PMID 29350227 DOI: 10.1039/C7Cc08620B |
0.848 |
|
2018 |
Nwajiobi O, Raj M. SYNTHESIS OF FUNCTIONALIZED MACROCYCLIC PEPTIDES Frontiers in Chemistry. 6. DOI: 10.3389/Conf.Fchem.2018.01.00051 |
0.843 |
|
2017 |
Wu H, Handoko, Raj M, Arora PS. Iterative Design of a Biomimetic Catalyst for Amino Acid Thioester Condensation. Organic Letters. PMID 28891652 DOI: 10.1021/Acs.Orglett.7B02412 |
0.72 |
|
2017 |
Elashal HE, Sim YE, Raj M. Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation. Chemical Science. 8: 117-123. PMID 28451155 DOI: 10.1039/C6Sc02162J |
0.868 |
|
2016 |
Elashal HE, Cohen RD, Raj M. Fmoc solid-phase synthesis of C-terminal modified peptides by formation of a backbone cyclic urethane moiety. Chemical Communications (Cambridge, England). PMID 27407005 DOI: 10.1039/C6Cc04245G |
0.842 |
|
2016 |
Elashal HE, Raj M. Site-selective chemical cleavage of peptide bonds. Chemical Communications (Cambridge, England). 52: 6304-7. PMID 27087443 DOI: 10.1039/C6Cc01509C |
0.873 |
|
2016 |
Nalbone JM, Lahankar N, Buissereth L, Raj M. Glutamic Acid Selective Chemical Cleavage of Peptide Bonds. Organic Letters. 18: 1186-9. PMID 26866465 DOI: 10.1021/Acs.Orglett.6B00317 |
0.8 |
|
2015 |
Raj M, Wu H, Blosser SL, Vittoria MA, Arora PS. Aldehyde capture ligation for synthesis of native Peptide bonds. Journal of the American Chemical Society. 137: 6932-40. PMID 25966041 DOI: 10.1021/Jacs.5B03538 |
0.751 |
|
2013 |
Raj M, Bullock BN, Arora PS. Plucking the high hanging fruit: a systematic approach for targeting protein-protein interactions. Bioorganic & Medicinal Chemistry. 21: 4051-7. PMID 23267671 DOI: 10.1016/J.Bmc.2012.11.023 |
0.774 |
|
2011 |
Kaur J, Raj M, Cooperman BS. Fluorescent labeling of tRNA dihydrouridine residues: Mechanism and distribution. Rna (New York, N.Y.). 17: 1393-400. PMID 21628433 DOI: 10.1261/Rna.2670811 |
0.694 |
|
2010 |
Raj M, Veerasamy N, Singh VK. Highly enantioselective synthesis of 3-cycloalkanone-3-hydroxy-2-oxindoles, potential anticonvulsants Tetrahedron Letters. 51: 2157-2159. DOI: 10.1016/J.Tetlet.2010.02.082 |
0.548 |
|
2009 |
Raj M, Singh VK. Organocatalytic reactions in water. Chemical Communications (Cambridge, England). 6687-703. PMID 19885454 DOI: 10.1039/B910861K |
0.521 |
|
2009 |
Raj M, Parashari G, Singh V. Highly Enantioselective Organocatalyticsyn- andanti-Aldol Reactions in Aqueous Medium Advanced Synthesis & Catalysis. 351: 1284-1288. DOI: 10.1002/Adsc.200900122 |
0.549 |
|
2007 |
Maya V, Raj M, Singh VK. Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. Organic Letters. 9: 2593-5. PMID 17518481 DOI: 10.1021/Ol071013L |
0.479 |
|
2006 |
Raj M, Vishnumaya V, Ginotra SK, Singh VK. Highly enantioselective direct aldol reaction catalyzed by organic molecules. Organic Letters. 8: 4097-9. PMID 16928083 DOI: 10.1021/Ol0616081 |
0.531 |
|
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