Year |
Citation |
Score |
2024 |
Youmans DD, Moore AM, Stanley LM. Synthesis of Highly Substituted Oxaboroles from Oxaboranes via a Selective Petasis Borono-Mannich Reaction. Organic Letters. PMID 39172524 DOI: 10.1021/acs.orglett.4c02260 |
0.373 |
|
2022 |
Moore AS, Stanley LM. Nickel-Catalyzed Formation of α-Substituted γ-Amino Ketones via Alkene Carboacylation. Organic Letters. PMID 36460050 DOI: 10.1021/acs.orglett.2c03413 |
0.426 |
|
2022 |
Koeritz MT, Banovetz HK, Prell SA, Stanley LM. Synthesis of oxaboranes nickel-catalyzed dearylative cyclocondensation. Chemical Science. 13: 7790-7795. PMID 35865885 DOI: 10.1039/d2sc01840c |
0.438 |
|
2022 |
Tran HN, Stanley LM. Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes. Organic Letters. 24: 395-399. PMID 34905379 DOI: 10.1021/acs.orglett.1c04073 |
0.492 |
|
2021 |
Kadam AA, Metz TL, David CM, Koeritz MT, Stanley LM. Palladium-Catalyzed Intermolecular Acylative Heck Reactions with Imides as Acyl Electrophiles. The Journal of Organic Chemistry. PMID 33881868 DOI: 10.1021/acs.joc.1c00087 |
0.417 |
|
2021 |
Banovetz HK, Vickerman KL, David CM, Alkan M, Stanley LM. Palladium-Catalyzed Intermolecular Alkene Carboacylation via Ester C-O Bond Activation. Organic Letters. PMID 33843239 DOI: 10.1021/acs.orglett.1c00940 |
0.468 |
|
2021 |
Tran HN, Burgett RW, Stanley LM. Nickel-Catalyzed Asymmetric Hydroarylation of Vinylarenes: Direct Enantioselective Synthesis of Chiral 1,1-Diarylethanes. The Journal of Organic Chemistry. PMID 33576628 DOI: 10.1021/acs.joc.0c02556 |
0.522 |
|
2020 |
Koeritz MT, Burgett RW, Kadam AA, Stanley LM. Ni-Catalyzed Intermolecular Carboacylation of Internal Alkynes via Amide C-N Bond Activation. Organic Letters. 22: 5731-5736. PMID 32790418 DOI: 10.1021/Acs.Orglett.0C01607 |
0.552 |
|
2019 |
Kadam AA, Metz TL, Qian Y, Stanley LM. Ni-Catalyzed Three-Component Alkene Carboacylation Initiated by Amide C–N Bond Activation Acs Catalysis. 9: 5651-5656. DOI: 10.1021/Acscatal.9B01620 |
0.56 |
|
2019 |
Heintz PM, Schumacher BP, Chen M, Huang W, Stanley LM. A Pd(II)‐Functionalized Covalent Organic Framework for Catalytic Conjugate Additions of Arylboronic Acids to β,β‐Disubstituted Enones Chemcatchem. 11: 4286-4290. DOI: 10.1002/Cctc.201900894 |
0.326 |
|
2018 |
Metz TL, Lutovsky GA, Stanley LM. An Acid-Catalyzed Addition and Dehydration Sequence for the Synthesis of Heteroarylated Steroidal Dienes. The Journal of Organic Chemistry. PMID 29298060 DOI: 10.1021/Acs.Joc.7B03045 |
0.493 |
|
2018 |
Metz TL, Leng M, Evans J, Stanley LM. Synthesis of heteroarylated ketones via bismuth(III) triflate-promoted regioselective 1,4- and 1,6-additions of electron-rich heteroarenes to cyclic enones and dienones Tetrahedron. 74: 3283-3292. DOI: 10.1016/J.Tet.2018.04.002 |
0.387 |
|
2017 |
Li X, Zhang B, Tang L, Goh TW, Qi S, Volkov A, Pei Y, Qi Z, Tsung CK, Stanley L, Huang W. Cooperative Multifunctional Catalysts for Nitrone Synthesis: Platinum Nanoclusters in Amine-Functionalized Metal-Organic Frameworks. Angewandte Chemie (International Ed. in English). PMID 29065244 DOI: 10.1002/Anie.201710164 |
0.34 |
|
2017 |
Vickerman KL, Stanley LM. Catalytic, Enantioselective Synthesis of Polycyclic Nitrogen, Oxygen, and Sulfur Heterocycles via Rh-Catalyzed Alkene Hydroacylation. Organic Letters. PMID 28933168 DOI: 10.1021/Acs.Orglett.7B02230 |
0.551 |
|
2017 |
Kadam AA, Ellern A, Stanley LM. Enantioselective, Palladium-Catalyzed Conjugate Additions of Arylboronic Acids to Form Bis-benzylic Quaternary Stereocenters. Organic Letters. PMID 28737030 DOI: 10.1021/Acs.Orglett.7B01825 |
0.461 |
|
2017 |
Walker JA, Vickerman KL, Humke JN, Stanley LM. Nickel-Catalyzed Alkene Carboacylation via Activation of Amide C-N Bonds. Journal of the American Chemical Society. PMID 28708388 DOI: 10.1021/Jacs.7B06191 |
0.708 |
|
2017 |
Metz TL, Evans J, Stanley LM. Catalytic Conjugate Addition of Electron-Rich Heteroarenes to β,β-Disubstituted Enones. Organic Letters. PMID 28650646 DOI: 10.1021/Acs.Orglett.7B01402 |
0.389 |
|
2016 |
Walker JA, Stanley LM. N-Heterocyclic carbene-catalysed intramolecular hydroacylation to form basic nitrogen-containing heterocycles. Organic & Biomolecular Chemistry. PMID 27722422 DOI: 10.1039/C6Ob01956K |
0.468 |
|
2016 |
Johnson KF, Schneider EA, Schumacher BP, Ellern A, Scanlon JD, Stanley L. Rhodium-Catalyzed, Enantioselective Intramolecular Hydroacylation of Trisubstituted Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27572933 DOI: 10.1002/Chem.201603880 |
0.561 |
|
2016 |
Ghosh A, Bainbridge DT, Stanley LM. An Enantioselective Model Synthesis and Progress toward the Putative Structure of Yuremamine. The Journal of Organic Chemistry. PMID 27494137 DOI: 10.1021/Acs.Joc.6B01730 |
0.459 |
|
2016 |
Van Zeeland R, Li X, Huang W, Stanley LM. MOF-253-Pd(OAc)2: a recyclable MOF for transition-metal catalysis in water Rsc Advances. 6: 56330-56334. DOI: 10.1039/C6Ra12746K |
0.346 |
|
2016 |
Ghosh A, Johnson KF, Vickerman KL, Walker JA, Stanley LM. Recent advances in transition metal-catalysed hydroacylation of alkenes and alkynes Organic Chemistry Frontiers. 3: 639-644. DOI: 10.1039/C6Qo00023A |
0.404 |
|
2016 |
Gerten AL, Stanley LM. Enantioselective dearomative [3 + 2] cycloadditions of indoles with azomethine ylides derived from alanine imino esters Organic Chemistry Frontiers. 3: 339-343. DOI: 10.1039/C5Qo00346F |
0.527 |
|
2016 |
Li X, Van Zeeland R, Maligal-Ganesh RV, Pei Y, Power G, Stanley L, Huang W. Impact of Linker Engineering on the Catalytic Activity of Metal-Organic Frameworks Containing Pd(II)-Bipyridine Complexes Acs Catalysis. 6: 6324-6328. DOI: 10.1021/Acscatal.6B01753 |
0.381 |
|
2016 |
Ghosh A, Walker JA, Ellern A, Stanley LM. Coupling Catalytic Alkene Hydroacylation and α-Arylation: Enantioselective Synthesis of Heterocyclic Ketones with α-Chiral Quaternary Stereocenters Acs Catalysis. 6: 2673-2680. DOI: 10.1021/Acscatal.6B00365 |
0.531 |
|
2016 |
Gerten AL, Stanley LM. Palladium-catalyzed conjugate addition of arylboronic acids to 2-substituted chromones in aqueous media Tetrahedron Letters. 57: 5460-5463. DOI: 10.1016/J.Tetlet.2016.10.084 |
0.514 |
|
2016 |
Gerten AL, Stanley LM. ChemInform Abstract: Enantioselective Dearomative [3 + 2] Cycloadditions of Indoles with Azomethine Ylides Derived from Alanine Imino Esters. Cheminform. 47. DOI: 10.1002/chin.201627148 |
0.422 |
|
2015 |
Johnson KF, Schmidt AC, Stanley LM. Rhodium-Catalyzed, Enantioselective Hydroacylation of ortho-Allylbenzaldehydes. Organic Letters. PMID 26398100 DOI: 10.1021/Acs.Orglett.5B02559 |
0.539 |
|
2015 |
Du XW, Stanley LM. Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives. Organic Letters. PMID 26098453 DOI: 10.1021/Acs.Orglett.5B01447 |
0.564 |
|
2015 |
Van Zeeland R, Stanley LM. Palladium-Catalyzed Conjugate Addition of Arylboronic Acids to β,β-Disubstituted Enones in Aqueous Media: Formation of Bis-benzylic and ortho-Substituted Benzylic Quaternary Centers Acs Catalysis. 5: 5203-5206. DOI: 10.1021/Acscatal.5B01272 |
0.464 |
|
2014 |
Du XW, Ghosh A, Stanley LM. Enantioselective synthesis of polycyclic nitrogen heterocycles by Rh-catalyzed alkene hydroacylation: constructing six-membered rings in the absence of chelation assistance. Organic Letters. 16: 4036-9. PMID 25020184 DOI: 10.1021/Ol501869S |
0.524 |
|
2014 |
Ghosh A, Stanley LM. Enantioselective hydroacylation of N-vinylindole-2-carboxaldehydes. Chemical Communications (Cambridge, England). 50: 2765-8. PMID 24481054 DOI: 10.1039/C4Cc00210E |
0.561 |
|
2013 |
Gerten AL, Slade MC, Pugh KM, Stanley LM. Catalytic, enantioselective 1,3-dipolar cycloadditions of nitrile imines with methyleneindolinones. Organic & Biomolecular Chemistry. 11: 7834-7. PMID 24132663 DOI: 10.1039/C3Ob41815D |
0.55 |
|
2013 |
Johnson KF, Van Zeeland R, Stanley LM. Palladium-catalyzed synthesis of N-tert-prenylindoles. Organic Letters. 15: 2798-801. PMID 23714013 DOI: 10.1021/Ol4011344 |
0.455 |
|
2013 |
Johnson KF, Van Zeeland R, Stanley LM. ChemInform Abstract: Palladium-Catalyzed Synthesis of N-tert-Prenylindoles. Cheminform. 44: no-no. DOI: 10.1002/chin.201340110 |
0.372 |
|
2011 |
Liao X, Stanley LM, Hartwig JF. Enantioselective total syntheses of (-)-taiwaniaquinone H and (-)-taiwaniaquinol B by iridium-catalyzed borylation and palladium-catalyzed asymmetric α-arylation. Journal of the American Chemical Society. 133: 2088-91. PMID 21268578 DOI: 10.1021/Ja110215B |
0.538 |
|
2011 |
Stanley LM, Sibi MP. Chiral Bisoxazoline Ligands Privileged Chiral Ligands and Catalysts. 171-219. DOI: 10.1002/9783527635207.ch5 |
0.526 |
|
2010 |
Hartwig JF, Stanley LM. Mechanistically driven development of iridium catalysts for asymmetric allylic substitution. Accounts of Chemical Research. 43: 1461-75. PMID 20873839 DOI: 10.1021/Ar100047X |
0.557 |
|
2010 |
Stanley LM, Bai C, Ueda M, Hartwig JF. Iridium-catalyzed kinetic asymmetric transformations of racemic allylic benzoates. Journal of the American Chemical Society. 132: 8918-20. PMID 20552969 DOI: 10.1021/Ja103779E |
0.582 |
|
2010 |
Hartwig J, Stanley L, Bai C, Ueda M. Kinetic Asymmetric Substitution of Racemic Allylic Esters Synfacts. 2010: 1163-1163. DOI: 10.1055/s-0030-1258643 |
0.448 |
|
2010 |
Sibi MP, Cruzjr W, Stanley LM. Enantioselective diels-alder cycloadditions with -substituted pyrazolidinone propiolimides Synlett. 889-892. DOI: 10.1055/S-0029-1219538 |
0.717 |
|
2009 |
Stanley LM, Hartwig JF. Iridium-catalyzed regio- and enantioselective N-allylation of indoles. Angewandte Chemie (International Ed. in English). 48: 7841-4. PMID 19760689 DOI: 10.1002/Anie.200904338 |
0.54 |
|
2009 |
Pouy MJ, Stanley LM, Hartwig JF. Enantioselective, iridium-catalyzed monoallylation of ammonia. Journal of the American Chemical Society. 131: 11312-3. PMID 19722644 DOI: 10.1021/Ja905059R |
0.545 |
|
2009 |
Sibi MP, Kawashima K, Stanley LM. Diels-Alder cycloaddition strategy for kinetic resolution of chiral pyrazolidinones. Organic Letters. 11: 3894-7. PMID 19650642 DOI: 10.1021/Ol901504P |
0.659 |
|
2009 |
Stanley LM, Hartwig JF. Regio- and enantioselective N-allylations of imidazole, benzimidazole, and purine heterocycles catalyzed by single-component metallacyclic iridium complexes. Journal of the American Chemical Society. 131: 8971-83. PMID 19480431 DOI: 10.1021/Ja902243S |
0.548 |
|
2009 |
Sibi M, Kawashima K, Stanley L. Kinetic Resolution of Pyrazolidinones by a Cu(II)-Catalyzed Diels-Alder Reaction Synfacts. 2009: 1367-1367. DOI: 10.1055/s-0029-1218314 |
0.561 |
|
2009 |
Sibi M, Coulomb J, Stanley L. Enantioselective Protonation of Friedel-Crafts Intermediates Synfacts. 2009: 0302-0302. DOI: 10.1055/s-0028-1087773 |
0.563 |
|
2009 |
Sibi MP, Kawashima K, Stanley LM. Diels-alder cycloaddition strategy for kinetic resolution of chiral pyrazolidinones Organic Letters. 11: 3894-3897. DOI: 10.1021/ol901504p |
0.584 |
|
2008 |
Sibi MP, Coulomb J, Stanley LM. Enantioselective enolate protonations: Friedel-Crafts reactions with alpha-substituted acrylates. Angewandte Chemie (International Ed. in English). 47: 9913-5. PMID 19016291 DOI: 10.1002/Anie.200804221 |
0.611 |
|
2008 |
Stanley LM, Sibi MP. Enantioselective copper-catalyzed 1,3-dipolar cycloadditions Chemical Reviews. 108: 2887-2902. PMID 18613728 DOI: 10.1021/Cr078371M |
0.644 |
|
2008 |
Sibi MP, Rane D, Stanley LM, Soeta T. Copper(II)-catalyzed exo and enantioselective cycloadditions of azomethine imines. Organic Letters. 10: 2971-4. PMID 18549218 DOI: 10.1021/Ol800904T |
0.77 |
|
2008 |
Sibi MP, Nie X, Shackleford JP, Stanley LM, Bouret F. Exo- and enantioselective Diels-Alder reactions: Pyrazolidinone auxiliaries as a means to enhanced exo selectivity Synlett. 2655-2658. DOI: 10.1055/S-0028-1083438 |
0.705 |
|
2008 |
Sibi MP, Rane D, Stanley LM, Soeta T. Copper(II)-catalyzed exo and enantioselective cycloadditions of azomethine imines Organic Letters. 10: 2971-2974. DOI: 10.1021/ol800904t |
0.587 |
|
2008 |
Sibi MP, Coulomb J, Stanley LM. Enantioselective enolate protonations: Friedel-crafts reactions with α-substituted acrylates Angewandte Chemie - International Edition. 47: 9913-9915. DOI: 10.1002/anie.200804221 |
0.609 |
|
2007 |
Sibi MP, Stanley LM, Soeta T. Enantioselective 1,3-dipolar cycloadditions of diazoacetates with electron-deficient olefins Organic Letters. 9: 1553-1556. PMID 17367154 DOI: 10.1021/Ol070364X |
0.569 |
|
2007 |
Sibi MP, Stanley LM, Nie X, Venkatraman L, Liu M, Jasperse CP. The role of achiral pyrazolidinone templates in enantioselective Diels-Alder reactions: Scope, limitations, and conformational insights Journal of the American Chemical Society. 129: 395-405. PMID 17212420 DOI: 10.1021/Ja066425O |
0.707 |
|
2007 |
Sibi M, Chen J, Stanley L. Effect of Achiral Templates in Enantioselective Diels-Alder Reactions Synfacts. 2007: 0401-0401. DOI: 10.1055/s-2007-968383 |
0.609 |
|
2007 |
Sibi MP, Chen J, Stanley L. Enantioselective diels-alder reactions: Effect of the achiral template on reactivity and selectivity Synlett. 298-302. DOI: 10.1055/S-2007-968014 |
0.668 |
|
2007 |
Sibi M, Stanley L, Soeta T. Chiral Dihydropyrazoles via Mg(II)-Catalyzed Nitrile Imine Cycloaddition Synfacts. 2007: 0175-0175. DOI: 10.1055/S-2006-955852 |
0.567 |
|
2007 |
Sibi MP, Chen J, Stanley L. Enantioselective Diels—Alder Reactions: Effect of the Achiral Template on Reactivity and Selectivity. Cheminform. 38. DOI: 10.1002/chin.200725056 |
0.388 |
|
2006 |
Sibi MP, Stanley LM, Soeta T. Enantioselective 1,3-dipolar cycloaddition of nitrile imines to α-substituted and α,β-disubstituted α,β-unsaturated carbonyl substrates: A method for synthesizing dihydropyrazoles bearing a chiral quaternary center Advanced Synthesis and Catalysis. 348: 2371-2375. DOI: 10.1002/Adsc.200600307 |
0.583 |
|
2005 |
Sibi MP, Stanley LM, Jasperse CP. An entry to a chiral dihydropyrazole scaffold: enantioselective [3 + 2] cycloaddition of nitrile imines. Journal of the American Chemical Society. 127: 8276-7. PMID 15941248 DOI: 10.1021/Ja051650B |
0.676 |
|
2005 |
Sibi MP, Stanley LM, Jasperse CP. An entry to a chiral dihydropyrazole scaffold: Enantioselective [3 + 2] cycloaddition of nitrile imines Journal of the American Chemical Society. 127: 8276-8277. DOI: 10.1021/ja051650b |
0.623 |
|
2004 |
Sibi MP, Stanley LM. Enantioselective diethylzinc additions to aldehydes catalyzed by chiral relay ligands Tetrahedron Asymmetry. 15: 3353-3356. DOI: 10.1016/J.Tetasy.2004.09.006 |
0.633 |
|
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