Year |
Citation |
Score |
2022 |
Dixon GJ, Rodriguez MR, Chong TG, Kim KY, Downey CW. Synthesis of β,β-Disubstituted Styrenes via Trimethylsilyl Trifluoromethanesulfonate-Promoted Aldehyde-Aldehyde Aldol Coupling-Elimination. The Journal of Organic Chemistry. PMID 36239694 DOI: 10.1021/acs.joc.2c01458 |
0.337 |
|
2021 |
Oracheff ZZ, Xia HL, Poff CD, Isaacson SE, Downey CW. Friedel-Crafts Addition of Indoles to Nitrones Promoted by Trimethylsilyl Trifluoromethanesulfonate. The Journal of Organic Chemistry. PMID 34780184 DOI: 10.1021/acs.joc.1c01551 |
0.85 |
|
2020 |
Downey CW, Glist HM, Takashima A, Bottum SR, Dixon GJ. Corrigendum to “Chalcone and cinnamate synthesis via one-pot enol silane formation-Mukaiyama aldol reactions of ketones and acetate esters” [Tetrahedron Lett. 59(32) (2018) 3080–3083] Tetrahedron Letters. 61: 152669. DOI: 10.1016/j.tetlet.2020.152669 |
0.62 |
|
2020 |
Downey CW, Robertson GAL, Santa J, Flicker KR, Stith WM. One-pot silyl ketene imine formation-nucleophilic addition reactions of acetonitrile with acetals and nitrones Tetrahedron Letters. 61: 151537. DOI: 10.1016/j.tetlet.2019.151537 |
0.841 |
|
2019 |
Downey CW, Dixon GJ, Ingersoll JA, Fuller CN, MacCormac KW, Takashima A, Sediqui R. One-pot enol silane formation-Mukaiyama aldol reactions: Crossed aldehyde-aldehyde coupling, thioester substrates, and reactions in ester solvents Tetrahedron Letters. 60: 151192. DOI: 10.1016/j.tetlet.2019.151192 |
0.824 |
|
2018 |
Downey CW, Confair DN, Liu Y, Heafner ED. One-Pot Enol Silane Formation-Alkylation of Ketones with Propargyl Carboxylates Promoted by Trimethylsilyl Trifluoromethanesulfonate. The Journal of Organic Chemistry. PMID 30248260 DOI: 10.1021/acs.joc.8b01997 |
0.832 |
|
2018 |
Downey CW, Glist HM, Takashima A, Bottum SR, Dixon GJ. Chalcone and cinnamate synthesis via one-pot enol silane formation-Mukaiyama aldol reactions of ketones and acetate esters Tetrahedron Letters. 59: 3080-3083. DOI: 10.1016/j.tetlet.2018.06.066 |
0.852 |
|
2018 |
Downey CW, Johnson MW. Corrigendum to “A tandem enol silane Formation-Mukaiyama aldol reaction mediated by TMSOTf” [Tetrahedron Lett. 48 (2007) 3559–3562] Tetrahedron Letters. 59: 1268. DOI: 10.1016/J.Tetlet.2018.01.088 |
0.845 |
|
2017 |
Downey CW, Lee AY, Goodin JR, Botelho CJ, Stith WM. Mukaiyama addition of (trimethylsilyl)acetonitrile to dimethyl acetals mediated by trimethylsilyl trifluoromethanesulfonate Tetrahedron Letters. 58: 3496-3499. DOI: 10.1016/j.tetlet.2017.07.082 |
0.762 |
|
2016 |
Downey CW, Ingersoll JA, Glist HM, Dombrowski CM, Barnett AT. ChemInform Abstract: One-Pot Silyl Ketene Acetal-Formation Mukaiyama-Mannich Additions to Imines Mediated by Trimethylsilyl Trifluoromethanesulfonate. Cheminform. 47: no-no. DOI: 10.1002/chin.201615079 |
0.797 |
|
2015 |
Downey CW, Poff CD, Nizinski AN. Friedel-Crafts Hydroxyalkylation of Indoles Mediated by Trimethylsilyl Trifluoromethanesulfonate. The Journal of Organic Chemistry. 80: 10364-9. PMID 26393376 DOI: 10.1021/acs.joc.5b01681 |
0.808 |
|
2014 |
van Loon AA, Holton MK, Downey CR, White TM, Rolph CE, Bruening SR, Li G, Delaney KM, Pelkey SJ, Pelkey ET. Preparation of dibenzo[e,g]isoindol-1-ones via Scholl-type oxidative cyclization reactions. The Journal of Organic Chemistry. 79: 8049-58. PMID 25138638 DOI: 10.1021/jo501185f |
0.335 |
|
2014 |
Downey CW, Covington SE, Obenschain DC, Halliday E, Rague JT, Confair DN. Silyl trifluoromethanesulfonate-activated para-methoxybenzyl methyl ether as an alkylating agent for thiols and aryl ketones Tetrahedron Letters. 55: 5213-5215. DOI: 10.1016/j.tetlet.2014.07.068 |
0.736 |
|
2014 |
Downey CW, Maxwell EN, Confair DN. Silyl triflate-accelerated additions of catalytically generated zinc acetylides to N-phenyl nitrones Tetrahedron Letters. 4959-4961. DOI: 10.1016/j.tetlet.2014.07.015 |
0.736 |
|
2013 |
Downey CW, Dombrowski CM, Maxwell EN, Safran CL, Akomah OA. One-pot enol silane formation/mukaiyama-mannich addition of ketones, amides, and thioesters to nitrones in the presence of trialkylsilyl trifluoromethanesulfonates European Journal of Organic Chemistry. 5716-5720. DOI: 10.1002/ejoc.201300691 |
0.808 |
|
2013 |
Downey CW, Craciun S, Neferu AM, Vivelo CA, Mueller CJ, Southall BC, Corsi S, Etchill EW, Sault R. ChemInform Abstract: One-Pot Synthesis of (Z)-β-Sulfonyl Enoates from Ethyl Propiolate. Cheminform. 44: no-no. DOI: 10.1002/chin.201304053 |
0.716 |
|
2013 |
Downey CW, Craciun S, Vivelo CA, Neferu AM, Mueller CJ, Corsi S. ChemInform Abstract: One-Pot Three-Step Thioconjugate Addition-Oxidation-Diels-Alder Reactions of Ethyl Propiolate. Cheminform. 44: no-no. DOI: 10.1002/chin.201303073 |
0.799 |
|
2012 |
Downey CW, Craciun S, Vivelo CA, Neferu AM, Mueller CJ, Corsi S. One-pot three-step thioconjugate addition-oxidation-Diels-Alder reactions of ethyl propiolate Tetrahedron Letters. 53: 5766-5768. DOI: 10.1016/j.tetlet.2012.08.054 |
0.792 |
|
2012 |
Downey CW, Craciun S, Neferu AM, Vivelo CA, Mueller CJ, Southall BC, Corsi S, Etchill EW, Sault RJ. One-pot synthesis of (Z)-β-sulfonyl enoates from ethyl propiolate Tetrahedron Letters. 53: 5763-5765. DOI: 10.1016/j.tetlet.2012.08.051 |
0.707 |
|
2011 |
Greger JG, Yoon-Miller SJ, Bechtold NR, Flewelling SA, MacDonald JP, Downey CR, Cohen EA, Pelkey ET. Synthesis of unsymmetrical 3,4-diaryl-3-pyrrolin-2-ones utilizing pyrrole Weinreb amides. The Journal of Organic Chemistry. 76: 8203-14. PMID 21913662 DOI: 10.1021/jo2013516 |
0.547 |
|
2011 |
Greger JG, Yoon-Miller SJ, Bechtold NR, Flewelling SA, MacDonald JP, Downey CR, Cohen EA, Pelkey ET. Synthesis of unsymmetrical 3,4-diaryl-3-pyrrolin-2-ones utilizing pyrrole Weinreb amides. The Journal of Organic Chemistry. 76: 8203-14. PMID 21913662 DOI: 10.1021/jo2013516 |
0.547 |
|
2011 |
Downey CW, Fleisher AS, Rague JT, Safran CL, Venable ME, Pike RD. Synthesis of N-acyl-N,O-acetals from N-aryl amides and acetals in the presence of TMSOTf Tetrahedron Letters. 52: 4756-4759. DOI: 10.1016/J.Tetlet.2011.07.023 |
0.795 |
|
2010 |
Downey CW, Johnson MW, Lawrence DH, Fleisher AS, Tracy KJ. Acetic acid aldol reactions in the presence of trimethylsilyl trifluoromethanesulfonate. The Journal of Organic Chemistry. 75: 5351-4. PMID 20590083 DOI: 10.1021/Jo100828C |
0.837 |
|
2010 |
Evans DA, Tedrow JS, Shaw JT, Downey CW. ChemInform Abstract: Diastereoselective Magnesium Halide-Catalyzed anti-Aldol Reactions of Chiral N-Acyloxazolidinones. Cheminform. 33: no-no. DOI: 10.1002/chin.200226034 |
0.846 |
|
2010 |
Evans DA, Scheidt KA, Downey CW. ChemInform Abstract: Synthesis of (-)-Epibatidine Cheminform. 33: no-no. DOI: 10.1002/chin.200204220 |
0.803 |
|
2009 |
Downey CW, Mahoney BD, Lipari VR. Trimethylsilyl trifluoromethanesulfonate-accelerated addition of catalytically generated zinc acetylides to aldehydes. The Journal of Organic Chemistry. 74: 2904-6. PMID 19260695 DOI: 10.1021/jo900102w |
0.804 |
|
2008 |
Downey CW, Johnson MW, Tracy KJ. One-pot enol silane formation-Mukaiyama aldol-type addition to dimethyl acetals mediated by TMSOTf. The Journal of Organic Chemistry. 73: 3299-302. PMID 18335962 DOI: 10.1021/Jo8001084 |
0.875 |
|
2008 |
O'Halloran N, James JP, Downey CA, O'Malley P, Duff T, Bertrand S. Inter-and intra-molecular cyclisation reactions of azoacetates derived from aryl hydrazones of ethyl acetoacetate and acetoacetanilides Heterocycles. 75: 2681-2701. DOI: 10.3987/COM-08-11433 |
0.528 |
|
2007 |
Downey CW, Johnson MW. A tandem enol silane formation-Mukaiyama aldol reaction mediated by TMSOTf Tetrahedron Letters. 48: 3559-3562. DOI: 10.1016/J.Tetlet.2007.03.088 |
0.87 |
|
2007 |
Downey CW, Johnson MW. A Tandem Enol Silane Formation—Mukaiyama Aldol Reaction Mediated by TMSOTf. Cheminform. 38. DOI: 10.1002/chin.200735102 |
0.747 |
|
2005 |
Suárez A, Downey CW, Fu GC. Kinetic resolutions of azomethine imines via copper-catalyzed [3 + 2] cycloadditions. Journal of the American Chemical Society. 127: 11244-5. PMID 16089444 DOI: 10.1021/Ja052876H |
0.822 |
|
2004 |
Smith TE, Djang M, Velander AJ, Downey CW, Carroll KA, Van Alphen S. Versatile asymmetric synthesis of the kavalactones: first synthesis of (+)-kavain. Organic Letters. 6: 2317-20. PMID 15228268 DOI: 10.1021/ol0493960 |
0.853 |
|
2003 |
Evans DA, Seidel D, Rueping M, Lam HW, Shaw JT, Downey CW. A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction. Journal of the American Chemical Society. 125: 12692-3. PMID 14558801 DOI: 10.1021/Ja0373871 |
0.84 |
|
2003 |
Evans DA, Downey CW, Hubbs JL. Ni(II) bis(oxazoline)-catalyzed enantioselective syn aldol reactions of N-propionylthiazolidinethiones in the presence of silyl triflates. Journal of the American Chemical Society. 125: 8706-7. PMID 12862448 DOI: 10.1021/Ja035509J |
0.849 |
|
2003 |
Kosmrlj J, Weigel LO, Evans DA, Downey CW, Wu J. Unfunctionalized, alpha-epimerizable nonracemic ketones and aldehydes can be accessed by crystallization-induced dynamic resolution of imines. Journal of the American Chemical Society. 125: 3208-9. PMID 12630864 DOI: 10.1021/Ja029715N |
0.794 |
|
2002 |
Evans DA, Downey CW, Shaw JT, Tedrow JS. Magnesium halide-catalyzed anti-aldol reactions of chiral N-acylthiazolidinethiones. Organic Letters. 4: 1127-30. PMID 11922799 DOI: 10.1021/Ol025553O |
0.856 |
|
2002 |
Evans DA, Tedrow JS, Shaw JT, Downey CW. Diastereoselective magnesium halide-catalyzed anti-aldol reactions of chiral N-acyloxazolidinones. Journal of the American Chemical Society. 124: 392-3. PMID 11792206 DOI: 10.1021/Ja0119548 |
0.848 |
|
2001 |
Evans DA, Scheidt KA, Downey CW. Synthesis of (-)-epibatidine. Organic Letters. 3: 3009-12. PMID 11554830 DOI: 10.1021/Ol016420Q |
0.86 |
|
2001 |
Evans DA, Rovis T, Kozlowski MC, Downey CW, Tedrow JS. ChemInform Abstract: Enantioselective Lewis Acid Catalyzed Michael Reactions of Alkylidene Malonates. Catalysis by C2-Symmetric Bis(oxazoline) Copper(II) Complexes in the Synthesis of Chiral, Differentiated Glutarate Esters. Cheminform. 32: no-no. DOI: 10.1002/chin.200103030 |
0.839 |
|
2000 |
Evans DA, Rovis T, Kozlowski MC, Downey CW, Tedrow JS. Enantioselective Lewis acid catalyzed Michael reactions of alkylidene malonates. Catalysis by C2-symmetric bis(oxazoline) copper(II) complexes in the synthesis of chiral, differentiated glutarate esters Journal of the American Chemical Society. 122: 9134-9142. DOI: 10.1021/Ja002246+ |
0.826 |
|
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