Year |
Citation |
Score |
2022 |
Dyadyuk A, Vershinin V, Shalit H, Shalev H, More NY, Pappo D. A Chiral Iron Disulfonate Catalyst for the Enantioselective Synthesis of 2-Amino-2'-hydroxy-1,1'-binaphthyls (NOBINs). Journal of the American Chemical Society. 144: 3676-3684. PMID 35167756 DOI: 10.1021/jacs.1c13020 |
0.332 |
|
2021 |
Mintz T, More NY, Gaster E, Pappo D. Iron-Catalyzed Oxidative Cross-Coupling of Phenols and Tyrosine Derivatives with 3-Alkyloxindoles. The Journal of Organic Chemistry. 86: 18164-18178. PMID 34881564 DOI: 10.1021/acs.joc.1c02435 |
0.364 |
|
2021 |
Vershinin V, Forkosh H, Ben-Lulu M, Libman A, Pappo D. Mechanistic Insights into the FeCl-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes. The Journal of Organic Chemistry. 86: 79-90. PMID 33296193 DOI: 10.1021/acs.joc.0c00874 |
0.326 |
|
2020 |
Solel E, Pappo D, Reany O, Mejuch T, Gershoni-Poranne R, Botoshansky M, Stanger A, Keinan E. Flat corannulene: when a transition state becomes a stable molecule. Chemical Science. 11: 13015-13025. PMID 34094486 DOI: 10.1039/d0sc04566g |
0.456 |
|
2020 |
Ben-Lulu M, Gaster E, Libman A, Pappo D. Corrigendum: Synthesis of Biaryl-Bridged Cyclic Peptides via Catalytic Oxidative Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). 59: 14722. PMID 33645006 DOI: 10.1002/anie.202009345 |
0.36 |
|
2020 |
Ben-Lulu M, Gaster E, Libman A, Pappo D. Synthesis of Biaryl-Bridged Cyclic Peptides via Catalytic Oxidative Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). 59: 4835-4839. PMID 31800136 DOI: 10.1002/anie.201913305 |
0.324 |
|
2020 |
Ben‐Lulu M, Gaster E, Libman A, Pappo D. Berichtigung: Synthesis of Biaryl‐Bridged Cyclic Peptides via Catalytic Oxidative Cross‐Coupling Reactions Angewandte Chemie. 132: 14831-14831. DOI: 10.1002/ange.202009345 |
0.309 |
|
2019 |
Shalit H, Dyadyuk A, Pappo D. Selective Oxidative Phenol Coupling by Iron Catalysis. The Journal of Organic Chemistry. 84: 1677-1686. PMID 30657316 DOI: 10.1021/acs.joc.8b03084 |
0.314 |
|
2018 |
Forkosh H, Vershinin V, Reiss H, Pappo D. Stereoselective Synthesis of Optically Pure 2-Amino-2'-hydroxy-1,1'-binaphthyls. Organic Letters. PMID 29608314 DOI: 10.1021/acs.orglett.8b00800 |
0.344 |
|
2018 |
Parnes R, Reiss H, Pappo D. Cu(OTf)-Catalyzed Pummerer Coupling of β-Ketosulfoxides. The Journal of Organic Chemistry. 83: 723-732. PMID 29293340 DOI: 10.1021/acs.joc.7b02708 |
0.324 |
|
2018 |
Keinan E, Pappo D. Organic Synthesis: From Glorious Past to Brilliant Future Israel Journal of Chemistry. 58: 7-10. DOI: 10.1002/Ijch.201800012 |
0.502 |
|
2017 |
Shalit H, Libman A, Pappo D. meso-Tetraphenylporphyrin Iron Chloride Catalyzed Selective Oxidative Cross-Coupling of Phenols. Journal of the American Chemical Society. PMID 28862442 DOI: 10.1021/jacs.7b05898 |
0.319 |
|
2017 |
Narute S, Pappo D. Iron Phosphate Catalyzed Asymmetric Cross-Dehydrogenative Coupling of 2-Naphthols with β-Ketoesters. Organic Letters. 19: 2917-2920. PMID 28498665 DOI: 10.1021/acs.orglett.7b01152 |
0.313 |
|
2017 |
Pappo D, Narute S, Parnes R, Toste F. Iron-Catalyzed Enantioselective Synthesis of BINOLs Synfacts. 13: 561-561. DOI: 10.1055/s-0036-1590380 |
0.313 |
|
2016 |
Narute S, Parnes R, Toste FD, Pappo D. Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes. Journal of the American Chemical Society. PMID 27959518 DOI: 10.1021/Jacs.6B11198 |
0.36 |
|
2016 |
Dyadyuk A, Sudheendran K, Vainer Y, Vershinin V, Shames AI, Pappo D. Direct Synthesis of Polyaryls by Consecutive Oxidative Cross-Coupling of Phenols with Arenes. Organic Letters. PMID 27529128 DOI: 10.1021/acs.orglett.6b02064 |
0.366 |
|
2015 |
Parnes R, Pappo D. Reductive Alkylation of Arenes by a Thiol-Based Multicomponent Reaction. Organic Letters. 17: 2924-7. PMID 26031511 DOI: 10.1021/acs.orglett.5b01142 |
0.34 |
|
2015 |
Gaster E, Vainer Y, Regev A, Narute S, Sudheendran K, Werbeloff A, Shalit H, Pappo D. Significant enhancement in the efficiency and selectivity of iron-catalyzed oxidative cross-coupling of phenols by fluoroalcohols. Angewandte Chemie (International Ed. in English). 54: 4198-202. PMID 25655277 DOI: 10.1002/anie.201409694 |
0.391 |
|
2015 |
Pappo D, Regev A, Shalit H. Iron-Catalyzed Oxidative C–C and C–O Coupling of Halophenols to α-Substituted β-Keto Esters Synthesis. 47: 1716-1725. DOI: 10.1055/S-0034-1380360 |
0.312 |
|
2014 |
Parnes R, Narute S, Pappo D. Thiol-promoted selective addition of ketones to aldehydes. Organic Letters. 16: 5922-5. PMID 25376009 DOI: 10.1021/ol502937n |
0.365 |
|
2014 |
Parvari G, Annamalai S, Borovoi I, Chechik H, Botoshansky M, Pappo D, Keinan E. Multifarenes: new modular cavitands. Chemical Communications (Cambridge, England). 50: 2494-7. PMID 24457352 DOI: 10.1039/C3Cc48284G |
0.477 |
|
2013 |
Kshirsagar UA, Parnes R, Goldshtein H, Ofir R, Zarivach R, Pappo D. Aerobic iron-based cross-dehydrogenative coupling enables efficient diversity-oriented synthesis of coumestrol-based selective estrogen receptor modulators. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13575-83. PMID 23946113 DOI: 10.1002/chem.201300389 |
0.659 |
|
2013 |
Kshirsagar UA, Regev C, Parnes R, Pappo D. Iron-catalyzed oxidative cross-coupling of phenols and alkenes. Organic Letters. 15: 3174-7. PMID 23758172 DOI: 10.1021/ol401532a |
0.666 |
|
2012 |
Parnes R, Kshirsagar UA, Werbeloff A, Regev C, Pappo D. Ligand-controlled iron-catalyzed coupling of α-substituted β-ketoesters with phenols. Organic Letters. 14: 3324-7. PMID 22694055 DOI: 10.1021/Ol301297K |
0.687 |
|
2012 |
Pogoreltsev A, Solel E, Pappo D, Keinan E. Deca-heterosubstituted corannulenes. Chemical Communications (Cambridge, England). 48: 5425-7. PMID 22543307 DOI: 10.1039/C2Cc31801F |
0.502 |
|
2009 |
Gershoni-Poranne R, Pappo D, Solel E, Keinan E. Corannulene ethers via Ullmann condensation. Organic Letters. 11: 5146-9. PMID 19905024 DOI: 10.1021/Ol902352K |
0.576 |
|
2009 |
Pappo D, Mejuch T, Reany O, Solel E, Gurram M, Keinan E. Diverse functionalization of corannulene: easy access to pentagonal superstructure. Organic Letters. 11: 1063-6. PMID 19193048 DOI: 10.1021/Ol8028127 |
0.558 |
|
2009 |
Goren L, Pappo D, Goldberg I, Kashman Y. Acyclic and cyclic thioenamino peptides: solution- and solid-phase synthesis Tetrahedron Letters. 50: 1048-1050. DOI: 10.1016/J.Tetlet.2008.12.072 |
0.468 |
|
2009 |
Kogon Y, Goren L, Pappo D, Rudi A, Kashman Y. Cyclic endiamino peptides: A new synthesis of imidazopyrazines European Journal of Organic Chemistry. 1852-1854. DOI: 10.1002/ejoc.200900008 |
0.521 |
|
2008 |
Nicolaou KC, Pappo D, Tsang KY, Gibe R, Chen DY. A chiral pool based synthesis of platensimycin. Angewandte Chemie (International Ed. in English). 47: 944-6. PMID 18176919 DOI: 10.1002/Anie.200705080 |
0.464 |
|
2007 |
Nicolaou KC, Li H, Nold AL, Pappo D, Lenzen A. Total synthesis of kinamycins C, F, and J. Journal of the American Chemical Society. 129: 10356-7. PMID 17676854 DOI: 10.1021/Ja074297D |
0.439 |
|
2007 |
Kashman Y, Rudi A, Pappo D. Recent heterocyclic compounds from marine invertebrates: Structure and synthesis Pure and Applied Chemistry. 79: 491-505. DOI: 10.1351/pac200779040491 |
0.485 |
|
2007 |
Nicolaou KC, Li H, Nold AL, Pappo D, Lenzen A. Synthesis of Kinamycin C Synfacts. 2007: 344-344. DOI: 10.1055/S-2007-968285 |
0.386 |
|
2006 |
Pappo D, Kashman Y. beta-turn mimetic: synthesis of cyclic thioenamino peptides. Organic Letters. 8: 1177-9. PMID 16524297 DOI: 10.1021/ol060075t |
0.484 |
|
2005 |
Pappo D, Vartanian M, Lang S, Kashman Y. Synthesis of cyclic endiamino peptides. Journal of the American Chemical Society. 127: 7682-3. PMID 15913350 DOI: 10.1021/ja050299r |
0.494 |
|
2005 |
Pappo D, Shimony S, Kashman Y. Synthesis of 9-substituted tetrahydrodiazepinopurines: studies toward the total synthesis of asmarines. The Journal of Organic Chemistry. 70: 199-206. PMID 15624923 DOI: 10.1021/jo048622g |
0.517 |
|
2003 |
Pappo D, Kashman Y. Synthesis of 9-substituted tetrahydrodiazepinopurines—asmarine A analogues Tetrahedron. 59: 6493-6501. DOI: 10.1016/S0040-4020(03)01058-5 |
0.575 |
|
2003 |
Pappo D, Kashman Y. Synthesis of 9-Substituted Tetrahydrodiazepinopurines—Asmarine A Analogues. Cheminform. 34. DOI: 10.1002/CHIN.200349196 |
0.575 |
|
2001 |
Pappo D, Rudi A, Kashman Y. A synthetic approach towards the synthesis of asmarine analogues Tetrahedron Letters. 42: 5941-5943. DOI: 10.1016/S0040-4039(01)01111-X |
0.529 |
|
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