☰

cached image

Anita E. Mattson - Publications

Affiliations: 
Chemistry and Biochemistry Ohio State University, Columbus, Columbus, OH 
Area:
Synthetic Methods
Website:
http://chemistry.osu.edu/faculty/mattson
Tree Info Similar researchers PubMed Report error

44 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Attard JW, Noel JR, Guan Y, Mattson AE. Enantioselective Access to Tetrahydroxanthones via Copper-(oxazoline)-Catalyzed [4 + 2] Cycloaddition. Organic Letters. PMID 37018061 DOI: 10.1021/acs.orglett.3c00612  0.305
2022 Guan Y, Buivydas T, Lalisse RF, Ali R, Hadad C, Mattson AE. Enantioselective Dearomative Alkynylation of Chromanones: Opportunities and Obstacles. Synthesis. 54: 4210-4219. PMID 36744023 DOI: 10.1055/a-1811-8075  0.321
2022 Leveille AN, Allegrezza MM, Laybourn K, Mattson AE. Dearomatization of benzopyrylium triflates with sulfoxonium ylides. Chemical Communications (Cambridge, England). 58: 12600-12603. PMID 36285765 DOI: 10.1039/d2cc02023h  0.42
2021 Leveille AN, Echemendía R, Mattson AE, Burtoloso ACB. Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides. Organic Letters. 23: 9446-9450. PMID 34854689 DOI: 10.1021/acs.orglett.1c03627  0.381
2020 Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S-H Insertion Reactions of α-Carbonyl Sulfoxonium Ylides. Angewandte Chemie (International Ed. in English). PMID 32352184 DOI: 10.1002/Anie.202005563  0.331
2019 Guan Y, Attard J, Mattson AE. Copper Bis(oxazoline)-Catalyzed Enantioselective Alkynylation of Benzopyrylium Ions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31867810 DOI: 10.1002/chem.201904822  0.307
2018 Guan Y, Attard JW, Visco MD, Fisher TJ, Mattson AE. Enantioselective Catalyst Systems from Copper(II) Triflate and BINOL-Silanediol. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29575279 DOI: 10.1002/chem.201801304  0.406
2017 Visco MD, Attard J, Guan Y, Mattson AE. Anion-binding catalyst designs for enantioselective synthesis Tetrahedron Letters. 58: 2623-2628. DOI: 10.1016/j.tetlet.2017.05.045  0.321
2016 Hardman-Baldwin AM, Visco MD, Wieting JM, Stern C, Kondo SI, Mattson AE. Silanediol-Catalyzed Chromenone Functionalization. Organic Letters. PMID 27453257 DOI: 10.1021/Acs.Orglett.6B01783  0.419
2016 Visco MD, Wieting JM, Mattson AE. Carbon-Silicon Bond Formation in the Synthesis of Benzylic Silanes. Organic Letters. PMID 27255675 DOI: 10.1021/Acs.Orglett.6B01223  0.463
2016 Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent Roles of Urea and Phosphoric Acid Derived Catalysts in Reactions of Diazo Compounds Synthesis (Germany). 48: 677-686. DOI: 10.1055/S-0035-1561061  0.784
2016 Visco MD, Reeves JT, Marsini MA, Volchkov I, Busacca CA, Mattson AE, Senanayake CH. Triisopropyl borate mediated N-sulfinyl imine formation Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2016.03.063  0.444
2016 Sieber JD, Angeles-Dunham VV, Chennamadhavuni D, Fandrick DR, Haddad N, Grinberg N, Kurouski D, Lee H, Song JJ, Yee NK, Mattson AE, Senanayake CH. Rhodium-Catalyzed Asymmetric Allenylation of Sulfonylimines and Application to the Stereospecific Allylic Allenylation Advanced Synthesis and Catalysis. 358: 3062-3068. DOI: 10.1002/Adsc.201600686  0.517
2015 Reeves JT, Visco MD, Marsini MA, Grinberg N, Busacca CA, Mattson AE, Senanayake CH. A General Method for Imine Formation Using B(OCH2CF3)3. Organic Letters. 17: 2442-5. PMID 25906082 DOI: 10.1021/Acs.Orglett.5B00949  0.328
2015 Wieting JM, Fisher TJ, Schafer AG, Visco MD, Gallucci JC, Mattson AE. Preparation and catalytic activity of BINOL-derived silanediols European Journal of Organic Chemistry. 2015: 525-533. DOI: 10.1002/Ejoc.201403441  0.687
2014 Angeles-Dunham VV, Nickerson DM, Ray DM, Mattson AE. Nitrimines as reagents for metal-free formal C(sp(2) )-C(sp(2) ) cross-coupling reactions. Angewandte Chemie (International Ed. in English). 53: 14538-41. PMID 25365926 DOI: 10.1002/Anie.201408613  0.65
2014 Hardman-Baldwin AM, Mattson AE. Silanediol-catalyzed carbon dioxide fixation. Chemsuschem. 7: 3275-8. PMID 25328125 DOI: 10.1002/Cssc.201402783  0.326
2014 Fisher TJ, Mattson AE. Synthesis of α-peroxyesters via organocatalyzed O-H insertion of hydroperoxides and aryl diazoesters. Organic Letters. 16: 5316-9. PMID 25265196 DOI: 10.1021/Ol502494H  0.412
2014 Couch ED, Auvil TJ, Mattson AE. Urea-induced acid amplification: a new approach for metal-free insertion chemistry. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8283-7. PMID 24889759 DOI: 10.1002/Chem.201403283  0.779
2014 So SS, Oottikkal S, Badji? JD, Hadad CM, Mattson AE. Urea-catalyzed N-H insertion-arylation reactions of nitrodiazoesters. The Journal of Organic Chemistry. 79: 4832-42. PMID 24797352 DOI: 10.1021/Jo500698Q  0.708
2014 Auvil TJ, Schafer AG, Mattson AE. Design Strategies for Enhanced Hydrogen-Bond Donor Catalysts (Eur. J. Org. Chem. 13/2014) European Journal of Organic Chemistry. 2014: n/a-n/a. DOI: 10.1002/Ejoc.201490033  0.78
2014 Auvil TJ, Schafer AG, Mattson AE. Design strategies for enhanced hydrogen-bond donor catalysts European Journal of Organic Chemistry. 2014: 2633-2646. DOI: 10.1002/Ejoc.201400035  0.797
2014 So SS, Mattson AE. Stereoselective N-H insertion-arylation reactions of nitrodiazoesters Asian Journal of Organic Chemistry. 3: 425-428. DOI: 10.1002/Ajoc.201300285  0.704
2013 Nickerson DM, Angeles VV, Mattson AE. Urea activation of nitrimines: a mild, metal-free approach to sterically hindered enamines. Organic Letters. 15: 5000-3. PMID 24070092 DOI: 10.1021/Ol402310B  0.726
2013 Schafer AG, Wieting JM, Fisher TJ, Mattson AE. Chiral silanediols in anion-binding catalysis. Angewandte Chemie (International Ed. in English). 52: 11321-4. PMID 24039105 DOI: 10.1002/Anie.201305496  0.658
2013 Auvil TJ, So SS, Mattson AE. Arylation of diazoesters by a transient N-H insertion organocascade. Angewandte Chemie (International Ed. in English). 52: 11317-20. PMID 24038873 DOI: 10.1002/Anie.201304921  0.779
2013 Hardman AM, So SS, Mattson AE. Urea-catalyzed construction of oxazinanes. Organic & Biomolecular Chemistry. 11: 5793-7. PMID 23907178 DOI: 10.1039/C3Ob41517A  0.671
2013 Nickerson DM, Angeles VV, Auvil TJ, So SS, Mattson AE. Internal Lewis acid assisted ureas: tunable hydrogen bond donor catalysts. Chemical Communications (Cambridge, England). 49: 4289-91. PMID 23198283 DOI: 10.1039/C2Cc37073E  0.784
2012 Nickerson DM, Mattson AE. Transition metal and hydrogen bond donor hybrids: catalysts for the activation of alkylidene malonates. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 8310-4. PMID 22692954 DOI: 10.1002/Chem.201201206  0.691
2012 So SS, Mattson AE. Urea activation of α-nitrodiazoesters: an organocatalytic approach to N-H insertion reactions. Journal of the American Chemical Society. 134: 8798-801. PMID 22568726 DOI: 10.1021/Ja3031054  0.688
2012 So SS, Auvil TJ, Garza VJ, Mattson AE. Boronate urea activation of nitrocyclopropane carboxylates. Organic Letters. 14: 444-7. PMID 22208166 DOI: 10.1021/Ol202873D  0.803
2012 Auvil TJ, Mattson AE. Internal Lewis acid assisted benzoic acid catalysis Synthesis (Germany). 44: 2173-2180. DOI: 10.1055/S-0031-1291048  0.782
2011 Schafer AG, Wieting JM, Mattson AE. Silanediols: a new class of hydrogen bond donor catalysts. Organic Letters. 13: 5228-31. PMID 21894881 DOI: 10.1021/Ol2021115  0.712
2011 So SS, Burkett JA, Mattson AE. Internal Lewis acid assisted hydrogen bond donor catalysis. Organic Letters. 13: 716-9. PMID 21226464 DOI: 10.1021/Ol102899Y  0.708
2011 Gu C, Mahasenan KV, Auvil T, Joshi K, Gupta S, Mattson A, Li C, Nakano I. Abstract 3298: Structure-based computer-aided drug design to discover novel small molecules that target brain tumor stem cells Cancer Research. 71: 3298-3298. DOI: 10.1158/1538-7445.Am2011-3298  0.71
2010 Crimmins MT, Shamszad M, Mattson AE. A highly convergent approach toward (-)-brevenal. Organic Letters. 12: 2614-7. PMID 20446718 DOI: 10.1021/Ol1008203  0.757
2009 Mathies AK, Mattson AE, Scheidt KA. Intermolecular Cross-Acyloin Reactions by Fluoride-Promoted Additions of O-Silyl Thiazolium Carbinols. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2009: 377-383. PMID 21132061 DOI: 10.1055/S-0028-1087555  0.771
2007 Mattson AE, Scheidt KA. Nucleophilic acylation of o-quinone methides: an umpolung strategy for the synthesis of alpha-aryl ketones and benzofurans. Journal of the American Chemical Society. 129: 4508-9. PMID 17378561 DOI: 10.1021/Ja068189N  0.621
2006 Mattson AE, Bharadwaj AR, Zuhl AM, Scheidt KA. Thiazolium-catalyzed additions of acylsilanes: a general strategy for acyl anion addition reactions. The Journal of Organic Chemistry. 71: 5715-24. PMID 16839153 DOI: 10.1021/Jo060699C  0.738
2006 Mattson AE, Zuhl AM, Reynolds TE, Scheidt KA. Direct nucleophilic acylation of nitroalkenes promoted by a fluoride anion/thiourea combination. Journal of the American Chemical Society. 128: 4932-3. PMID 16608309 DOI: 10.1021/Ja056565I  0.756
2006 Scheidt K, Mattson A, Zuhl A, Reynolds T. Direct Nucleophilic Acylation of Nitroalkenes Synfacts. 2006: 0616-0616. DOI: 10.1055/S-2006-941785  0.703
2004 Mattson AE, Scheidt KA. Catalytic additions of acylsilanes to imines: an acyl anion strategy for the direct synthesis of alpha-amino ketones. Organic Letters. 6: 4363-6. PMID 15524484 DOI: 10.1021/Ol0481129  0.641
2004 Mattson AE, Bharadwaj AR, Scheidt KA. The thiazolium-catalyzed Sila-Stetter reaction: conjugate addition of acylsilanes to unsaturated esters and ketones. Journal of the American Chemical Society. 126: 2314-5. PMID 14982429 DOI: 10.1021/Ja0318380  0.767
2004 Mattson AE, Scheidt KA. Catalytic additions of acylsilanes to imines: An acyl anion strategy for the direct synthesis of α-amino ketones Organic Letters. 6: 4363-4366.  0.582
Show low-probability matches.