Year |
Citation |
Score |
2023 |
Chauhan P, V R, Kumar M, Molla R, Mishra SD, Basa S, Rai V. Chemical technology principles for selective bioconjugation of proteins and antibodies. Chemical Society Reviews. PMID 38095227 DOI: 10.1039/d3cs00715d |
0.853 |
|
2023 |
Molla R, Joshi PN, Reddy NC, Biswas D, Rai V. Protein-Protein Interaction in Multicomponent Reaction Enables Chemoselective, Site-Selective, and Modular Labeling of Native Proteins. Organic Letters. PMID 37603545 DOI: 10.1021/acs.orglett.3c02405 |
0.864 |
|
2023 |
Chauhan P, V R, Kumar M, Molla R, V B U, Rai V. istegrate (DIN) Theory Enabling Precision Engineering of Proteins. Acs Central Science. 9: 137-150. PMID 36844488 DOI: 10.1021/acscentsci.2c01455 |
0.816 |
|
2022 |
Thakur K, T K S, Singh SK, V R, Rawale DG, Adusumalli SR, Kalra N, Shukla S, Mishra RK, Rai V. Human Behavior-Inspired Linchpin-Directed Catalysis for Traceless Precision Labeling of Lysine in Native Proteins. Bioconjugate Chemistry. PMID 36383773 DOI: 10.1021/acs.bioconjchem.2c00454 |
0.838 |
|
2022 |
Sahu T, Kumar M, T K S, Joshi M, Mishra RK, Rai V. Residue-specific N-terminal glycine to aldehyde transformation renders analytically pure single-site labeled proteins. Chemical Communications (Cambridge, England). PMID 36278269 DOI: 10.1039/d2cc04196k |
0.805 |
|
2022 |
Reddy NC, Molla R, Joshi PN, T K S, Basu I, Kawadkar J, Kalra N, Mishra RK, Chakrabarty S, Shukla S, Rai V. Traceless cysteine-linchpin enables precision engineering of lysine in native proteins. Nature Communications. 13: 6038. PMID 36229616 DOI: 10.1038/s41467-022-33772-1 |
0.864 |
|
2022 |
Bal A, Singh SK, Kashyap T, Rai V. Linchpin-directed precise labeling of lysine in native proteins, purification, and analysis. Methods in Enzymology. 675: 383-396. PMID 36220278 DOI: 10.1016/bs.mie.2022.07.016 |
0.748 |
|
2022 |
Sahu T, Chilamari M, Rai V. Protein inspired chemically orthogonal imines for linchpin directed precise and modular labeling of lysine in proteins. Chemical Communications (Cambridge, England). PMID 35037678 DOI: 10.1039/d1cc05559c |
0.868 |
|
2021 |
Adakkattil R, Thakur K, Rai V. Reactivity and Selectivity Principles in Native Protein Bioconjugation. Chemical Record (New York, N.Y.). PMID 34184826 DOI: 10.1002/tcr.202100108 |
0.868 |
|
2021 |
Kumar M, Reddy NC, Rai V. Chemical technologies for precise protein bioconjugation interfacing biology and medicine. Chemical Communications (Cambridge, England). PMID 34180471 DOI: 10.1039/d1cc02268g |
0.838 |
|
2021 |
Rawale DG, Thakur K, Sreekumar P, T K S, A R, Adusumalli SR, Mishra RK, Rai V. Linchpins empower promiscuous electrophiles to enable site-selective modification of histidine and aspartic acid in proteins. Chemical Science. 12: 6732-6736. PMID 34040749 DOI: 10.1039/d1sc00335f |
0.854 |
|
2020 |
Purushottam L, V B U, Rawale DG, Gujrati M, Mishra SD, T K S, Reddy NC, Adusumalli SR, Mishra RK, Rai V. A single amino acid Gly-tag enables metal-free protein purification. Chemical Science. 11: 13137-13142. PMID 34094495 DOI: 10.1039/d0sc01153c |
0.792 |
|
2020 |
Reddy NC, Kumar M, Molla R, Rai V. Chemical methods for modification of proteins. Organic & Biomolecular Chemistry. PMID 32538424 DOI: 10.1039/D0Ob00857E |
0.842 |
|
2020 |
Adusumalli SR, Rawale DG, Thakur K, Purushottam L, Reddy NC, Kalra N, Shukla S, Rai V. Chemoselective and Site-Selective Lysine-Directed Lysine Modification Enables Single-Site Labeling of Native Proteins. Angewandte Chemie (International Ed. in English). PMID 32171045 DOI: 10.1002/Anie.202000062 |
0.827 |
|
2020 |
Rai V, Upmanyu V, Mohd G, Kumar R, Koppad S, Sachdeva HS, Ansari A, Nautiyal S, Bora DP, Pandey AB, Dhar P, Tiwari AK. Comparing the efficiency of different Escherichia coli strains in producing recombinant capsid protein of porcine circovirus type 2. Molecular and Cellular Probes. 101556. PMID 32126262 DOI: 10.1016/j.mcp.2020.101556 |
0.331 |
|
2020 |
Gupta N, Ansari A, Dhoke GV, Chilamari M, Sivaccumar J, Kumari S, Chatterjee S, Goyal R, Dutta PK, Samarla M, Mukherjee M, Sarkar A, Mandal SK, Rai V, Biswas G, et al. Author Correction: Computationally designed antibody-drug conjugates self-assembled via affinity ligands. Nature Biomedical Engineering. PMID 31900467 DOI: 10.1038/S41551-019-0511-3 |
0.763 |
|
2019 |
Gupta N, Ansari A, Dhoke GV, Chilamari M, Sivaccumar J, Kumari S, Chatterjee S, Goyal R, Dutta PK, Samarla M, Mukherjee M, Sarkar A, Mandal SK, Rai V, Biswas G, et al. Computationally designed antibody-drug conjugates self-assembled via affinity ligands. Nature Biomedical Engineering. PMID 31686001 DOI: 10.1038/S41551-019-0470-8 |
0.787 |
|
2019 |
Singudas R, Reddy NC, Rai V. Sensitivity booster for mass detection enables unambiguous analysis of peptides, proteins, antibodies, and protein bioconjugates. Chemical Communications (Cambridge, England). PMID 31367719 DOI: 10.1039/C9Cc03424B |
0.792 |
|
2019 |
Purushottam L, Adusumalli SR, Singh U, Unnikrishnan VB, Rawale DG, Gujrati M, Mishra RK, Rai V. Single-site glycine-specific labeling of proteins. Nature Communications. 10: 2539. PMID 31182711 DOI: 10.1038/S41467-019-10503-7 |
0.853 |
|
2019 |
Joshi PN, Rai V. Single-site labeling of histidine in proteins, on-demand reversibility, and traceless metal-free protein purification. Chemical Communications (Cambridge, England). PMID 30620346 DOI: 10.1039/C8Cc08733D |
0.822 |
|
2019 |
Rawale DG, Thakur K, Adusumalli SR, Rai V. Chemical Methods for Selective Labeling of Proteins European Journal of Organic Chemistry. 2019: 6749-6763. DOI: 10.1002/Ejoc.201900801 |
0.838 |
|
2018 |
Adusumalli SR, Rawale DG, Rai V. Aldehydes can switch the chemoselectivity of electrophiles in protein labeling. Organic & Biomolecular Chemistry. 16: 9377-9381. PMID 30516786 DOI: 10.1039/C8Ob02897D |
0.866 |
|
2018 |
Adusumalli SR, Rawale DG, Singh U, Tripathi P, Paul R, Kalra N, Mishra RK, Shukla S, Rai V. Single-site labeling of native proteins enabled by a chemoselective and site-selective chemical technology. Journal of the American Chemical Society. PMID 30336012 DOI: 10.1021/Jacs.8B10490 |
0.82 |
|
2018 |
Chilamari M, Kalra N, Shukla S, Rai V. Single-site labeling of lysine in proteins through a metal-free multicomponent approach. Chemical Communications (Cambridge, England). PMID 29904775 DOI: 10.1039/C8Cc03311K |
0.847 |
|
2017 |
Chilamari M, Purushottam L, Rai V. Site-selective labeling of native proteins by a multicomponent approach. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28177162 DOI: 10.1002/Chem.201605938 |
0.85 |
|
2017 |
Purushottam L, Adusumalli SR, Chilamari M, Rai V. Chemoselective and site-selective peptide and native protein modification enabled by aldehyde auto-oxidation. Chemical Communications (Cambridge, England). PMID 28044167 DOI: 10.1039/C6Cc09555K |
0.814 |
|
2015 |
Zaretsky S, Rai V, Gish G, Forbes MW, Kofler M, Yu JC, Tan J, Hickey JL, Pawson T, Yudin AK. Twisted amide electrophiles enable cyclic peptide sequencing. Organic & Biomolecular Chemistry. PMID 26077966 DOI: 10.1039/C5Ob01050K |
0.567 |
|
2015 |
Singudas R, Adusumalli SR, Joshi PN, Rai V. A phthalimidation protocol that follows protein defined parameters. Chemical Communications (Cambridge, England). 51: 473-6. PMID 25429646 DOI: 10.1039/C4Cc08503E |
0.802 |
|
2015 |
Joshi PN, Purushottam L, Das NK, Mukherjee S, Rai V. Protein self-assembly induces promiscuous nucleophilic biocatalysis in Morita-Baylis-Hillman (MBH) reaction Rsc Advances. 6: 208-211. DOI: 10.1039/C5Ra23949D |
0.754 |
|
2014 |
Rotstein BH, Zaretsky S, Rai V, Yudin AK. Small heterocycles in multicomponent reactions. Chemical Reviews. 114: 8323-59. PMID 25032909 DOI: 10.1021/Cr400615V |
0.707 |
|
2012 |
Scully CC, Rai V, Poda G, Zaretsky S, Burns DC, Houliston RS, Lou T, Yudin AK. Bending rigid molecular rods: formation of oligoproline macrocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15612-7. PMID 23124621 DOI: 10.1002/Chem.201203266 |
0.536 |
|
2010 |
Rotstein BH, Rai V, Hili R, Yudin AK. Synthesis of peptide macrocycles using unprotected amino aldehydes. Nature Protocols. 5: 1813-22. PMID 21030956 DOI: 10.1038/Nprot.2010.127 |
0.738 |
|
2010 |
Jebrail MJ, Ng AH, Rai V, Hili R, Yudin AK, Wheeler AR. Synchronized synthesis of peptide-based macrocycles by digital microfluidics. Angewandte Chemie (International Ed. in English). 49: 8625-9. PMID 20715231 DOI: 10.1002/Anie.201001604 |
0.591 |
|
2010 |
Hili R, Rai V, Yudin AK. Macrocyclization of linear peptides enabled by amphoteric molecules. Journal of the American Chemical Society. 132: 2889-91. PMID 20155938 DOI: 10.1021/Ja910544P |
0.593 |
|
2010 |
Jebrail MJ, Ng AHC, Rai V, Hili R, Yudin AK, Wheeler AR. Inside Cover: Synchronized Synthesis of Peptide-Based Macrocycles by Digital Microfluidics (Angew. Chem. Int. Ed. 46/2010) Angewandte Chemie International Edition. 49: 8536-8536. DOI: 10.1002/Anie.201004588 |
0.537 |
|
2010 |
Jebrail MJ, Ng AHC, Rai V, Hili R, Yudin AK, Wheeler AR. Innentitelbild: Synchronized Synthesis of Peptide-Based Macrocycles by Digital Microfluidics (Angew. Chem. 46/2010) Angewandte Chemie. 122: 8716-8716. DOI: 10.1002/Ange.201004588 |
0.532 |
|
2009 |
Jebrail MJ, Ng A, Rai V, Hili R, Yudin AK, Wheeler AR. Synchronized synthesis of cyclic peptides by digital microfluidics Proceedings of Conference, Microtas 2009 - the 13th International Conference On Miniaturized Systems For Chemistry and Life Sciences. 1297-1299. |
0.471 |
|
2008 |
Rai V, Namboothiri IN. Enantioselective conjugate addition of dialkyl phosphites to nitroalkenes Tetrahedron: Asymmetry. 19: 2335-2338. DOI: 10.1016/J.Tetasy.2008.10.010 |
0.346 |
|
2008 |
Rai V, Namboothiri IN. Effect of achiral and mixed chiral ligands on the asymmetric synthesis of γ-nitrophosphonates via Michael addition Tetrahedron: Asymmetry. 19: 767-772. DOI: 10.1016/J.Tetasy.2008.03.006 |
0.388 |
|
2007 |
Rai V, Mobin SM, Namboothiri IN. Cinchonine catalyzed diastereo- and enantioselective Michael addition of α-lithiated phosphonates to nitroalkenes Tetrahedron: Asymmetry. 18: 2719-2726. DOI: 10.1016/J.Tetasy.2007.11.001 |
0.342 |
|
2006 |
Rai V, Namboothiri INN. A Theoretical Evaluation of the Michael-Acceptor Ability of Conjugated Nitroalkenes European Journal of Organic Chemistry. 2006: 4693-4703. DOI: 10.1002/Ejoc.200600505 |
0.4 |
|
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