Year |
Citation |
Score |
2023 |
Maji A, Soutar CP, Zhang J, Lewandowska A, Uno BE, Yan S, Shelke Y, Murhade G, Nimerovsky E, Borcik CG, Arango AS, Lange JD, Marin-Toledo JP, Lyu Y, Bailey KL, et al. Tuning sterol extraction kinetics yields a renal-sparing polyene antifungal. Nature. PMID 37938782 DOI: 10.1038/s41586-023-06710-4 |
0.54 |
|
2022 |
Nicolaou KC, Pan S, Shelke Y, Rigol S, Bao R, Das D, Ye Q. A unified strategy for the total syntheses of eribulin and a macrolactam analogue of halichondrin B. Proceedings of the National Academy of Sciences of the United States of America. 119: e2208938119. PMID 35930662 DOI: 10.1073/pnas.2208938119 |
0.745 |
|
2021 |
Nicolaou KC, Pan S, Shelke Y, Ye Q, Das D, Rigol S. A Highly Convergent Total Synthesis of Norhalichondrin B. Journal of the American Chemical Society. PMID 34851106 DOI: 10.1021/jacs.1c10539 |
0.752 |
|
2021 |
Hande PE, Shelke YG, Datta A, Gharpure SJ. Recent Advances in Small Molecule-Based Intracellular pH Probes. Chembiochem : a European Journal of Chemical Biology. PMID 34695287 DOI: 10.1002/cbic.202100448 |
0.527 |
|
2021 |
Shelke YG, Hande PE, Gharpure SJ. Recent advances in the synthesis of pyrrolo[1,2-]indoles and their derivatives. Organic & Biomolecular Chemistry. 19: 7544-7574. PMID 34524330 DOI: 10.1039/d1ob01103k |
0.651 |
|
2021 |
Nicolaou KC, Pan S, Shelke Y, Das D, Ye Q, Lu Y, Sau S, Bao R, Rigol S. A Reverse Approach to the Total Synthesis of Halichondrin B. Journal of the American Chemical Society. PMID 34105959 DOI: 10.1021/jacs.1c05270 |
0.759 |
|
2020 |
Nicolaou KC, Shelke YG, Dherange BD, Kempema A, Lin B, Gu C, Sandoval J, Hammond M, Aujay M, Gavrilyuk J. Design, Synthesis, and Biological Investigation of Epothilone B Analogues Featuring Lactone, Lactam, and Carbocyclic Macrocycles, Epoxide, Aziridine, and 1,1-Difluorocyclopropane and Other Fluorine Residues. The Journal of Organic Chemistry. PMID 32065746 DOI: 10.1021/Acs.Joc.0C00123 |
0.748 |
|
2018 |
Gharpure SJ, Padmaja, Prasath V, Shelke YG. Cascade Radical Cyclization on Alkynyl Vinylogous Carbonates for the Divergent Synthesis of Tetrasubstituted Furans and Dihydrofurans. Organic Letters. PMID 30582819 DOI: 10.1021/Acs.Orglett.8B03668 |
0.658 |
|
2018 |
Kapdi A, Shelke YG, Yashmeen A, Gholap AVA, Gharpure SJ. Homogeneous Catalysis: Powerful Technology for the Modification of Important Bio Molecules. Chemistry, An Asian Journal. PMID 30063286 DOI: 10.1002/Asia.201801020 |
0.629 |
|
2017 |
Gharpure SJ, Shelke YG. Lewis Acid Mediated Cascade Friedel-Craft/Alkyne Indol-2-yl Cation Cyclization/Vinyl Cation Trapping for the Synthesis of N-Fused Indole Derivatives. Organic Letters. 19: 5406-5409. PMID 28937768 DOI: 10.1021/Acs.Orglett.7B02680 |
0.67 |
|
2017 |
Gharpure SJ, Shelke YG. Cascade Radical Cyclization of N-Propargylindoles: Substituents Dictate Stereoselective Formation of N-Fused Indolines versus Indoles. Organic Letters. 19: 5022-5025. PMID 28902520 DOI: 10.1021/Acs.Orglett.7B02005 |
0.668 |
|
2017 |
Gharpure SJ, Nanda SK, Padmaja, Shelke YG. Metal-free Hydroalkoxylation-Formal [4+2] Cycloaddition Cascade for the Synthesis of Ketals. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 10007-10012. PMID 28521074 DOI: 10.1002/Chem.201701659 |
0.632 |
|
2017 |
Gharpure SJ, Nanda SK, Adate PA, Shelke YG. Lewis Acid Promoted Oxonium Ion Driven Carboamination of Alkynes for the Synthesis of 4-Alkoxy Quinolines. The Journal of Organic Chemistry. 82: 2067-2080. PMID 28106403 DOI: 10.1021/Acs.Joc.6B02896 |
0.669 |
|
2015 |
Gharpure SJ, Shelke YG, Kumar DP. Counter-ion-dependent alkyne iminium ion cyclization for divergent synthesis of N-fused indolylidine, indole, and indoline derivatives promoted by the Lewis/Bronsted acid. Organic Letters. 17: 1926-9. PMID 25815709 DOI: 10.1021/Acs.Orglett.5B00615 |
0.632 |
|
2014 |
Gharpure SJ, Shelke YG, Reddy SRB. Synthesis of isochromene derivatives using an intramolecular benzylic C(sp3)–C(sp2) bond forming Heck reaction on vinylogous carbonates Rsc Advances. 4: 46962-46965. DOI: 10.1039/C4Ra08421G |
0.641 |
|
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