Year |
Citation |
Score |
2022 |
Kattamuri PV, Zhao J, Das TK, Siitonen JH, Morgan N, Ess DH, Kürti L. -Quasi-Favorskii Reaction: Construction of Highly Substituted Aziridines through a Concerted Multibond Rearrangement Process. Journal of the American Chemical Society. PMID 35674783 DOI: 10.1021/jacs.2c03805 |
0.764 |
|
2021 |
Serna AV, Kürti L, Siitonen JH. Synthesis of (±)-Setigerumine I: Biosynthetic Origins of the Elusive Racemic Papaveraceae Isoxazolidine Alkaloids*. Angewandte Chemie (International Ed. in English). PMID 34706137 DOI: 10.1002/anie.202111049 |
0.754 |
|
2021 |
Zhang J, Kürti L. Multi-layer 3D chirality: its enantioselective synthesis and aggregation-induced emission. National Science Review. 8: nwaa205. PMID 34691558 DOI: 10.1093/nsr/nwaa205 |
0.431 |
|
2021 |
Paudyal MP, Wang M, Siitonen JH, Hu Y, Yousufuddin M, Shen HC, Falck JR, Kürti L. Intramolecular N-Me and N-H aminoetherification for the synthesis of -unprotected 3-amino-O-heterocycles. Organic & Biomolecular Chemistry. PMID 33399609 DOI: 10.1039/d0ob02122a |
0.768 |
|
2020 |
Behnke NE, Siitonen JH, Chamness SA, Kürti L. Synthesis of Highly Substituted Cyclopropanes via the Quasi-Favorskii Rearrangement of α,α-Dichlorocyclobutanols. Organic Letters. PMID 32330043 DOI: 10.1021/Acs.Orglett.0C01229 |
0.771 |
|
2020 |
Lovato K, Bhakta U, Ng YP, Kürti L. O-Cyclopropyl hydroxylamines: gram-scale synthesis and utility as precursors for N-heterocycles. Organic & Biomolecular Chemistry. PMID 32319502 DOI: 10.1039/D0Ob00611D |
0.444 |
|
2020 |
Siitonen JH, Kattamuri PV, Yousufuddin M, Kürti L. Arylboronic Acid-Catalyzed -Allylation of Unprotected Oximes: Total Synthesis of -Me-Euphococcine. Organic Letters. PMID 32159964 DOI: 10.1021/Acs.Orglett.0C00727 |
0.799 |
|
2020 |
Siitonen JH, Lira S, Yousufuddin M, Kürti L. Total synthesis of isatindigotindoline C. Organic & Biomolecular Chemistry. PMID 32141462 DOI: 10.1039/D0Ob00270D |
0.772 |
|
2020 |
Zhang J, Kürti L. Multi-layer 3D chirality: its enantioselective synthesis and aggregation-induced emission (AIE) National Science Review. DOI: 10.1093/Nsr/Nwaa205 |
0.496 |
|
2020 |
Hilario-Martínez JC, Murillo F, Garcia-Mendez J, Dzib E, Sandoval-Ramírez J, Muñoz M, Bernès S, Kurti L, Duarte F, Fernández-Herrera MA, Merino G. trans-Hydroboration-Oxidation products in Δ5-steroids via a hydroboration-retro-hydroboration mechanism Chemical Science. DOI: 10.1039/D0Sc01701A |
0.327 |
|
2019 |
Bhakta U, Kattamuri PV, Siitonen JH, Alemany LB, Kürti L. Enantioselective Catalytic Allylation of Acyclic Ketiminoesters: Synthesis of α-Fully-Substituted Amino Esters. Organic Letters. PMID 31663756 DOI: 10.1021/Acs.Orglett.9B03574 |
0.768 |
|
2019 |
Behnke NE, Lovato K, Yousufuddin M, Kürti L. Ti-Mediated Synthesis of Spirocyclic NH-Azetidines from Oxime Ethers. Angewandte Chemie (International Ed. in English). PMID 31381840 DOI: 10.1002/Anie.201909151 |
0.478 |
|
2019 |
Lu S, Ng SVH, Lovato K, Ong JY, Poh SB, Ng XQ, Kürti L, Zhao Y. Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation. Nature Communications. 10: 3061. PMID 31296858 DOI: 10.1038/S41467-019-10940-4 |
0.427 |
|
2019 |
Kattamuri PV, Bhakta U, Siriwongsup S, Kwon DH, Alemany LB, Yousufuddin M, Ess DH, Kürti L. Synthesis of Structurally Diverse 3-, 4-, 5- and 6-Membered Heterocycles from Diisopropyl Iminomalonates and Soft C-Nucleophiles. The Journal of Organic Chemistry. PMID 31009563 DOI: 10.1021/Acs.Joc.9B00681 |
0.44 |
|
2019 |
Guo L, Liu F, Wang L, Yuan H, Feng L, Kürti L, Gao H. Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines. Organic Letters. PMID 30942599 DOI: 10.1021/Acs.Orglett.9B00927 |
0.721 |
|
2019 |
Zhou Z, Cheng QQ, Kürti L. Aza-Rubottom Oxidation: Synthetic Access to Primary α-Aminoketones. Journal of the American Chemical Society. PMID 30696241 DOI: 10.1021/Jacs.8B13818 |
0.507 |
|
2019 |
Zhou Z, Kürti L. Electrophilic Amination: An Update Synlett. 30: 1525-1535. DOI: 10.1055/S-0037-1611861 |
0.593 |
|
2018 |
Behnke NE, Kielawa R, Kwon DH, Ess DH, Kürti L. Direct Primary Amination of Alkylmetals with NH-Oxaziridine. Organic Letters. PMID 30525689 DOI: 10.1021/Acs.Orglett.8B03734 |
0.359 |
|
2018 |
Lovato K, Guo L, Xu QL, Liu F, Yousufuddin M, Ess DH, Kürti L, Gao H. Transition metal-free direct dehydrogenative arylation of activated C(sp)-H bonds: synthetic ambit and DFT reactivity predictions. Chemical Science. 9: 7992-7999. PMID 30450183 DOI: 10.1039/C8Sc02758G |
0.682 |
|
2018 |
Zhou Z, Behnke NE, Kürti L. Copper-Catalyzed Synthesis of Hindered Ethers from α-Bromo Carbonyl Compounds. Organic Letters. PMID 30113173 DOI: 10.1021/Acs.Orglett.8B02371 |
0.546 |
|
2017 |
Kattamuri PV, Yin J, Siriwongsup S, Kwon DH, Ess DH, Li Q, Li G, Yousufuddin M, Richardson PF, Sutton SC, Kürti L. Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon-Nitrogen Bond-Formation. Journal of the American Chemical Society. PMID 28648054 DOI: 10.1021/Jacs.7B05279 |
0.422 |
|
2017 |
Gao H, Zhou Z, Kwon DH, Coombs J, Jones S, Behnke NE, Ess DH, Kürti L. Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds. Nature Chemistry. 9: 681-688. PMID 28644470 DOI: 10.1038/Nchem.2672 |
0.751 |
|
2017 |
Ma Z, Zhou Z, Kürti L. Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids. Angewandte Chemie (International Ed. in English). PMID 28614619 DOI: 10.1002/Anie.201705530 |
0.545 |
|
2016 |
Zhou Z, Ma Z, Behnke NE, Gao H, Kürti L. Non-Deprotonative Primary and Secondary Amination of (Hetero)Arylmetals. Journal of the American Chemical Society. PMID 28004917 DOI: 10.1021/Jacs.6B12712 |
0.7 |
|
2016 |
Paudyal MP, Adebesin AM, Burt SR, Ess DH, Ma Z, Kürti L, Falck JR. Dirhodium-catalyzed C-H arene amination using hydroxylamines. Science (New York, N.Y.). 353: 1144-7. PMID 27609890 DOI: 10.1126/Science.Aaf8713 |
0.579 |
|
2016 |
Wang JZ, Zhou J, Xu C, Sun H, Kürti L, Xu QL. Symmetry in Cascade Chirality-Transfer Processes: A Catalytic Atroposelective Direct Arylation Approach to BINOL Derivatives. Journal of the American Chemical Society. PMID 27052566 DOI: 10.1021/Jacs.6B01458 |
0.483 |
|
2016 |
Frink LA, Berthod A, Xu QL, Gao H, Kurti L, Armstrong DW. Separation of 2-naphthol atropisomers on cyclofructan-based chiral stationary phases Journal of Liquid Chromatography and Related Technologies. 1-8. DOI: 10.1080/10826076.2016.1234395 |
0.633 |
|
2015 |
Breitbach AS, Lim Y, Xu QL, Kürti L, Armstrong DW, Breitbach ZS. Enantiomeric separations of α-aryl ketones with cyclofructan chiral stationary phases via high performance liquid chromatography and supercritical fluid chromatography. Journal of Chromatography. A. PMID 26687164 DOI: 10.1016/J.Chroma.2015.11.069 |
0.347 |
|
2015 |
Gao H, Xu QL, Keene C, Yousufuddin M, Ess DH, Kürti L. Practical Organocatalytic Synthesis of Functionalized Non-C2 -Symmetrical Atropisomeric Biaryls. Angewandte Chemie (International Ed. in English). PMID 26592491 DOI: 10.1002/Anie.201508419 |
0.719 |
|
2015 |
Kürti L. Organic chemistry. Streamlining amine synthesis. Science (New York, N.Y.). 348: 863-4. PMID 25999493 DOI: 10.1126/Science.Aab2812 |
0.359 |
|
2014 |
Gao H, Xu QL, Keene C, Kürti L. Scalable, transition-metal-free direct oxime O-arylation: rapid access to O-arylhydroxylamines and substituted benzo[b]furans. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8883-7. PMID 24953184 DOI: 10.1002/Chem.201403519 |
0.657 |
|
2014 |
Woods RM, Patel DC, Lim Y, Breitbach ZS, Gao H, Keene C, Li G, Kürti L, Armstrong DW. Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases. Journal of Chromatography. A. 1357: 172-81. PMID 24835594 DOI: 10.1016/J.Chroma.2014.04.080 |
0.66 |
|
2014 |
Gao H, Xu QL, Yousufuddin M, Ess DH, Kürti L. Rapid synthesis of fused N-heterocycles by transition-metal-free electrophilic amination of arene C-H bonds. Angewandte Chemie (International Ed. in English). 53: 2701-5. PMID 24481643 DOI: 10.1002/Anie.201309973 |
0.714 |
|
2014 |
Jat JL, Paudyal MP, Gao H, Xu QL, Yousufuddin M, Devarajan D, Ess DH, Kürti L, Falck JR. Direct stereospecific synthesis of unprotected N-H and N-Me aziridines from olefins. Science (New York, N.Y.). 343: 61-5. PMID 24385626 DOI: 10.1126/Science.1245727 |
0.703 |
|
2014 |
Frink LA, Khan MA, Kürti L, Falck JR, Paudyal MP, Jat JL, Armstrong DW. Enantiomeric Separations of N–H/N–Me Aziridines Utilizing GC and HPLC Chromatographia. 77: 1607-1612. DOI: 10.1007/S10337-014-2776-8 |
0.454 |
|
2013 |
Xu QL, Gao H, Yousufuddin M, Ess DH, Kürti L. Aerobic, transition-metal-free, direct, and regiospecific mono-α-arylation of ketones: synthesis and mechanism by DFT calculations. Journal of the American Chemical Society. 135: 14048-51. PMID 24003902 DOI: 10.1021/Ja4074563 |
0.723 |
|
2013 |
Li GQ, Gao H, Keene C, Devonas M, Ess DH, Kürti L. Organocatalytic aryl-aryl bond formation: an atroposelective [3,3]-rearrangement approach to BINAM derivatives. Journal of the American Chemical Society. 135: 7414-7. PMID 23659490 DOI: 10.1021/Ja401709K |
0.724 |
|
2013 |
Gao H, Ess DH, Yousufuddin M, Kürti L. Transition-metal-free direct arylation: synthesis of halogenated 2-amino-2'-hydroxy-1,1'-biaryls and mechanism by DFT calculations. Journal of the American Chemical Society. 135: 7086-9. PMID 23470200 DOI: 10.1021/Ja400897U |
0.71 |
|
2013 |
Keene C, Kürti L. Regiospecific synthesis of novel cyclic nitrostyrenes and 3-substituted 2-nitronaphthalenes Synthesis (Germany). 45: 1719-1729. DOI: 10.1055/S-0033-1338867 |
0.506 |
|
2013 |
Corey EJ, Kurti L. Enantioselective Chemical Synthesis: Methods, Logic, and Practice Enantioselective Chemical Synthesis: Methods, Logic, and Practice. 1-328. |
0.404 |
|
2012 |
Zhu C, Li G, Ess DH, Falck JR, Kürti L. Elusive metal-free primary amination of arylboronic acids: synthetic studies and mechanism by density functional theory. Journal of the American Chemical Society. 134: 18253-6. PMID 23082853 DOI: 10.1021/Ja309637R |
0.558 |
|
2009 |
Kürti L, Blewett MM, Corey EJ. Origin of enantioselectivity in the Jacobsen epoxidation of olefins. Organic Letters. 11: 4592-5. PMID 19754126 DOI: 10.1021/Ol901859D |
0.461 |
|
2009 |
Corey E, Czakó B, Kürti L, Mammoto A, Ingber D. Synthesis of Cortistatin Analogues Synfacts. 2009: 1316-1316. DOI: 10.1055/S-0029-1218326 |
0.479 |
|
2008 |
Kürti L, Czakó B, Corey EJ. A short, scalable synthesis of the carbocyclic core of the anti-angiogenic cortistatins from (+)-estrone by B-ring expansion. Organic Letters. 10: 5247-50. PMID 18959422 DOI: 10.1021/Ol802328N |
0.545 |
|
2008 |
Kürti L, Chein RJ, Corey EJ. Conformational energetics of cationic backbone rearrangements in triterpenoid biosynthesis provide an insight into enzymatic control of product. Journal of the American Chemical Society. 130: 9031-6. PMID 18558677 DOI: 10.1021/Ja800980H |
0.485 |
|
2007 |
Smith AB, Kürti L, Davulcu AH, Cho YS, Ohmoto K. Indole diterpene synthetic studies: development of a second-generation synthetic strategy for (+)-nodulisporic acids A and B. The Journal of Organic Chemistry. 72: 4611-20. PMID 17511508 DOI: 10.1021/Jo062423A |
0.799 |
|
2007 |
Smith AB, Davulcu AH, Cho YS, Ohmoto K, Kürti L, Ishiyama H. Indole diterpene synthetic studies. Total synthesis of (+)-nodulisporic acid F and construction of the heptacyclic cores of (+)-nodulisporic acids A and B and (-)-nodulisporic acid D. The Journal of Organic Chemistry. 72: 4596-610. PMID 17511507 DOI: 10.1021/Jo062422I |
0.787 |
|
2007 |
Smith AB, Kürti L, Davulcu AH, Cho YS. Development of a scalable synthesis of a common eastern tricyclic lactone for construction of the nodulisporic acids Organic Process Research and Development. 11: 19-24. DOI: 10.1021/Op060204L |
0.814 |
|
2006 |
Smith AB, Kürti L, Davulcu AH. A new modular indole synthesis. Construction of the highly strained CDEF parent tetracycle of nodulisporic acids A and B. Organic Letters. 8: 2167-70. PMID 16671808 DOI: 10.1021/Ol0606536 |
0.793 |
|
2006 |
Smith AB, Davulcu AH, Kürti L. Indole diterpenoid synthetic studies. Construction of the heptacyclic core of (-)-nodulisporic acid D. Organic Letters. 8: 1669-72. PMID 16597137 DOI: 10.1021/Ol0602912 |
0.788 |
|
2006 |
Smith AB, Davulcu AH, Kürti L. Indole diterpenoid synthetic studies. The total synthesis of (+)-nodulisporic acid F. Organic Letters. 8: 1665-8. PMID 16597136 DOI: 10.1021/Ol060290+ |
0.797 |
|
2006 |
Smith, III A, Kürti L, Davulcu A. Modular Synthesis of Fused Indole Derivatives Synfacts. 2006: 0889-0889. DOI: 10.1055/s-2006-949206 |
0.794 |
|
2003 |
Kurti L, Papagiannopoulou D, Papadopoulos M, Pirmettis I, Raptopoulou CP, Terzis A, Chiotellis E, Harmata M, Kuntz RR, Pandurangi RS. Synthesis and characterization of novel 99gTc(V) and Re(V) complexes with water-soluble tetraaza diamido dipyridino ligands: single-crystal X-ray structural investigations of mono- and dinuclear complexes. Inorganic Chemistry. 42: 2960-7. PMID 12716188 DOI: 10.1021/Ic020434Q |
0.515 |
|
2002 |
Harmata M, Bohnert G, Kürti L, Barnes CL. Intramolecular 4+3 cycloadditions. A cyclohexenyl cation, its halogenated congener and a quasi-Favorskii rearrangement Tetrahedron Letters. 43: 2347-2349. DOI: 10.1016/S0040-4039(02)00264-2 |
0.801 |
|
2001 |
Harmata M, Barnes CL, Brackley J, Bohnert G, Kirchhoefer P, Kürti L, Rashatasakhon P. Generation of cyclopentadienones from 2-bromocyclopentenones Journal of Organic Chemistry. 66: 5232-5236. PMID 11463277 DOI: 10.1021/Jo015671+ |
0.687 |
|
2000 |
Juhász L, Kürti L, Antus S. Simple synthesis of benzofuranoid neolignans from Myristica fragrans. Journal of Natural Products. 63: 866-70. PMID 10869224 DOI: 10.1021/Np990327H |
0.466 |
|
1999 |
Harmata M, Shao L, Kürti L, Abeywardane A. 4+3 Cycloaddition reactions of halogen-substituted cyclohexenyl oxyallylic cations Tetrahedron Letters. 40: 1075-1078. DOI: 10.1016/S0040-4039(98)02629-X |
0.61 |
|
1999 |
Kürti L, Szilágyi L, Antus S, Nógrádi M. Oxidation of o‐Methoxyphenols with a Hypervalent Iodine Reagent: Improved Synthesis of Asatone and Demethoxyasatone European Journal of Organic Chemistry. 1999: 2579-2581. DOI: 10.1002/(Sici)1099-0690(199910)1999:10<2579::Aid-Ejoc2579>3.0.Co;2-H |
0.339 |
|
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