{"id":50,"date":"2017-04-04T15:29:17","date_gmt":"2017-04-04T15:29:17","guid":{"rendered":"http:\/\/gustafsongroup.sdsu.edu\/wordpress\/?page_id=50"},"modified":"2026-01-25T23:33:00","modified_gmt":"2026-01-25T23:33:00","slug":"publications","status":"publish","type":"page","link":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\t\t
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Publications as Professor at San Diego State University<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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44) “CySP3-96 enables scalable, streamlined, and low-cost sample preparation for cysteine chemoproteomic applications<\/span>” Shikwana, F.; Heydari, B.; Ofori, S.; Truong, C.; Turmon, A.; Darrouj, J.; Holoidovsky, L; Gustafson, J.; Backus, K. ChemRxiv. <\/i><\/span> <\/span>2024<\/span><\/strong>\u00a0<\/span>(link<\/a>)<\/p>

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43) “Targeting the RET tyrosine kinase in neuroblastoma: A review and application of a novel selective drug design strategy” Steen, E.; Basilaia, M.; Kim, W.; Getz, T.; Gustafson, J. Biochemical Pharmacology. <\/i><\/span> <\/span>2023<\/span><\/strong>, 216<\/span>, 115751<\/span> <\/span>(link<\/a>)<\/p>\n

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42) “A Light-Promoted Innate Trifluoromethylation of Pyridones and Related N-Heteroarenes.” Dang-Nguyen, A.; Legaspi, K. C.; McCarty, C. T.; Smith, D. K.; Gustafson, J. Org. Lett.<\/i><\/span>\u00a0<\/span>2023<\/span><\/strong>, 25<\/span>, 26<\/span>, 4898\u20134902 <\/span>(link<\/a>)<\/p>

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41) “Controlling Ibrutinib’s Conformations about Its Heterobiaryl Axis to Increase BTK Selectivity.” Toenjes, S. T.; Heydari, B. S.; Albright, S. T.; Hazin, R.; Ortiz, M. A.; Piedrafita, J.; Gustafson, J.\u00a0ACS Med. Chem. Lett.<\/i> 2023<\/strong>. 14, 3, 305\u2013311. (link<\/a>)<\/span><\/p>

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40) “Selective Functionalization of Arenes and Heteroarenes via SEAr and Related Transformations” Nguyen, A. D.; Zanolini, R. J,; Gustafson, J.L. Contributed chapter to book published by Wiley titled \u2018Handbook of C-H Functionalization\u2019. 2022.<\/strong> (Link<\/a>)<\/span><\/span><\/p>

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39) “Atropisomerism in the Pharmaceutically Relevant Realm” Basilaia, M.; Chen, H. M.; Secka, J.;\u00a0 Gustafson, J. L. Acc. Chem. Res. <\/em>2022,<\/b> 55, 20, 2904\u20132919<\/em>\u00a0(<\/span>Link<\/a>)<\/span><\/span><\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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38) “Approaches toward Atropisomerically Stable and Conformationally Pure Diarylamines” Vaidya, S. D.; Heydari, B. S.; Toenjes, S. T.;\u00a0 Gustafson, J. L. \u00a0<\/b>J. Org. Chem. <\/em>2022,<\/b> 87, 10, <\/em>6760\u20136768 (<\/span>Link<\/a>)<\/span><\/span><\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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37) “Catalytic Atroposelective Dynamic Kinetic Resolutions and Kinetic Resolutions towards 3-arylquinolines via SNAr ” Cardenas, M. C.; Saputra, M. A.; Gordon, D. A.; Sanchez, A. N.; Yamamoto, N.; Gustafson, J. L. Chem. Comm<\/em>. 2021<\/strong>.\u00a0<\/span><\/span>(<\/span>Link<\/a>)<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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36)\u00a0<\/span>\u201cAsymmetric Synthesis of Nonbiaryl Atropisomers\u201d Saputra, M. A.; Cardenas, M. C.; Gustafson, J. L. Contributed chapter to book published by Wiley titled \u2018Axially Chiral Compounds\u2019. 2021.<\/strong> (Link<\/a>)
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35) “Atropisomerism as Inspiration For New Chemistry” Cardenas, M.; Nguyen, A. D.; Brown, Z.; Heydari, B.; Heydari, B.; Vaidya, S.; Gustafson, J. Arkivoc<\/em>. 2021<\/strong>. i<\/em>. 20-47 (Link)<\/a>
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34) “Leveraging conformational control about a potential atropisomeric axis as a strategy in medical chemistry” Toenjes, Sean T., Mariam Basilaia, and Jeffrey L. Gustafson, Future Med. Chem. 2021<\/strong>, 13(5)<\/em>, 443-446. (Link<\/a>)<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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33) “Catalyst- Controlled Regioselective Chlorination of Phenols and Anilines through a Lewis Basic Selenoether Catalyst” Dinh, A.; Maddox, S.; Vaidya, S.; Saputra, M.; Nalbandian, C.; Gustafson, J. J. Org. Chem.<\/em> 2020<\/strong>, 85(21)<\/em>, 13895-13905 (Link<\/a>)<\/p>

Highlighted in SynFacts! (Link)<\/a>
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32) “Redox-Responsive H-Bonding: Amplifying the Effect of Electron Transfer Using Proton-Coupled Electron Transfer” Choi, H.; Baek, K.; Toenjes, S.; Gustafson, J.; Smith, D.\u00a0J. Am. Chem. Soc.,\u00a0<\/em>2020<\/strong>. (Link<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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31) “A Catalytic Cycle of Discovery: Asymmetric Catalysis Gives Rise to New Chiral Catalyst Scaffolds” Dinh, A. N. and Gustafson, J. L.\u00a0<\/span>Chem<\/em>,\u00a0<\/span>2020<\/strong>,\u00a0<\/span>6\u00a0<\/span><\/em>(4), 919-932. (<\/span>Link<\/a>)<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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30) “Discovery of Cyclic Guanidine-linked Sulfonamides as Inhibitors of LMTK3 kinase” Ortiz M. A.; Michaels, H.; Molina, B.; Toenjes, S.; Davis J.; Marconi G. D.; Hecht D.; Gustafson J. L.; Piedrafita, J. F.; Nefzi, A. Bioorganic & Medicinal Chemistry<\/em> Letters 2020<\/strong>, 30<\/em> (9), 127108. (Link<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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29) “Catalytic Atroposelective Synthesis of N-Aryl Quinoid Compounds” Vaidya, S. D.; Toenjes, S. T.; Yamamoto, N.; Maddox, S. M.; Gustafson J. L. J. Am. Chem. Soc.<\/em>, 2020<\/strong>, 142 <\/em>(5), 2198-2203. (Link<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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28) “Photocatalytic Oxidative C-H Thiolation: Synthesis of Benzothiazoles and Sulfenylated Indoles” Dinh, A. N.; Nguyen, A. D.; Millan Aceves, E.; Albright, S. T.; Cedano, M. R.; Smith, D. K.; Gustafson, J. L.\u00a0Synlett<\/i>\u00a02019<\/b>, 30<\/em> (14), 1648-1655 (Link<\/a>).<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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27) “Leveraging atropisomerism to Obtain a Selective Inhibitor of RET kinase with Secondary Activities towards EGFR Mutants” Toenjes S. T.; Garcia, V.; Maddox, S. M.; Dawson, G.A.; Ortiz, M. A.; Piedrafita, J.; Gustafson, J.L.\u00a0ACS Chem. Biol.<\/em>\u00a02019<\/strong>, 14 <\/em>(9), 1930-1939. (Link<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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26) “Toward a Catalytic Atroposelective Synthesis of Diaryl Ethers Through C(sp2)\u2013H Alkylation with Nitroalkanes” Dinh, A. N.; Noorbehesht, R. R.; Toenjes, S. T.; Jackson, A. C.; Saputra, M. A.; Maddox, S. M.; Gustafson, J. L.\u00a0Synlett<\/em>.\u00a02018<\/strong>. (doi:\u00a0https:\/\/doi.org\/10.1055\/s-0037-1609581<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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25) “Lewis Base\/Bronsted Acid Dual-Catalytic C\u2013H Sulfenylation of Aromatics” Nalbandian, C. J.; Brown, Z. E.; Alvarez, E.; Gustafson, J. L.\u00a0Org Lett<\/em>.\u00a02018<\/strong>,\u00a020<\/em>\u00a0(11), 3211\u20133214. (doi:\u00a0https:\/\/doi.org\/10.1021\/acs.orglett.8b01066<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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24) “Enantioselective Synthesis of Biaryl Atropisomers via the Addition of Thiophenols into Aryl-Naphthoquinones” Maddox, S. M.; Dawson, G. A.; Rochester, N. C.; Ayonon, A. B.; Moore, C. E.; Rheingold, A. L; Gustafson. J. L.\u00a0ACS Catal.<\/em>\u00a02018<\/strong>,\u00a08<\/em>, 5443\u20135447. (doi:\u00a0https:\/\/doi.org\/10.1021\/acscatal.8b00906<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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23) “Enantioselective Synthesis of Pyrrolopyrimidine Scaffolds through Cation-Directed Nucleophilic Aromatic Substitution” Cardenas, M. M.; Toenjes, S. T.; Nalbandian, C. J.; Gustafson, J. L.\u00a0Org. Lett<\/em>.\u00a02018<\/strong>,\u00a020<\/em>, 2037-2041.\u00a0<\/strong>(doi:\u00a0https:\/\/doi.org\/10.1021\/acs.orglett.8b00579<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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22) “Atropisomerism in medicinal chemistry: challenges and opportunities” Toenjes, S. T.; Gustafson, J. L.\u00a0Future Med.<\/em>\u00a0Chem<\/em>.\u00a02018<\/strong>,\u00a010<\/em>(4<\/em>), 409-422. (doi:\u00a0<\/strong>https:\/\/doi.org\/10.4155\/fmc-2017-0152<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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21) “Benzylic bromination catalyzed by triphenylphosphine selenide via Lewis basic activation” Ayonon, A; Nalbandian, C. J.; Guillemard, L.; Gustafson, J. L. Tetrahedron Lett.<\/i>\u00a02017,\u00a0<\/b>58<\/i>, 2940-2943. (doi:\u00a0https:\/\/doi.org\/10.1016\/j.tetlet.2017.06.042<\/a>)<\/span>\u00a0 \u00a0\u00a0<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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20) \u201cA conjugate Lewis base-Br\u00f8nsted acid catalyst for the sulfenylation of nitrogen containing heterocycles under mild conditions\u201d Nalbandian, C. J.; Miller, E. M.; Toenjes, S. T.; Gustafson, J. L.\u00a0Chem. Commun.\u00a0<\/em>2017,\u00a0<\/strong>53<\/em>, 1494-1497. (doi:\u00a0https:\/\/doi.org\/10.1039\/C6CC09998J<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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19)\u00a0\u201cThe Catalyst Controlled Regiodivergent Chlorination of Phenols\u201d Maddox, S. M.; Dinh, A, N.; Armenta, F.; Um, J.; Gustafson, J. L.\u00a0Org. Lett.\u00a0<\/em>2016,\u00a0<\/strong>18<\/em>, 5476. [Highlighted in\u00a0Synfacts,\u00a0<\/em>Jan 2017], (doi:\u00a0https:\/\/doi.org\/10.1021\/acs.orglett.6b02650<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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18) \u201cWater mediated Wittig Reactions of Aldehydes in the teaching laboratory: using sodium Bicarbonate for the in situ formation of stabilized ylides\u201d Kelley, M. J. B.; Fallot, L. B.; Gustafson, J. L.; Bergdahl, B. M.\u00a0J. Chem. Ed.\u00a0<\/em>2016<\/strong>,\u00a093<\/em>, 1631-1636. (doi:\u00a0https:\/\/doi.org\/10.1021\/acs.jchemed.6b00206<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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17) \u00a0\u201cEnhancing the selectivity of kinase inhibitors in oncology: A Chemical Biology Perspective\u201d Maddox, S. M.; Hecht, D. E.; Gustafson, J. L.\u00a0Future Med. Chem.\u00a0<\/em>2016<\/strong>,\u00a08<\/em>, 241-244. (doi:\u00a0https:\/\/doi.org\/10.4155\/fmc.15.193<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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16) \u00a0\u201cThe preorganization of Atropisomers to Increase target Selectivity.\u201d Nalbandian, C. J.; Hecht, D. E.; Gustafson, J. L.;\u00a0Syn. Lett.\u00a0<\/em>2016<\/strong>, 27, 977-983. (doi:\u00a0https:\/\/doi.org\/10.1055\/s-0035-1561314<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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15)\u00a0\u00a0\u201cExploiting Atropisomerism to Increase the Target Selectivity of Kinase Inhibitors\u201d Smith, D. E.; Marquez, I.; Lokensgard, M.; Rheingold, A. L, Hecht, D.;\u00a0Gustafson, Jeffrey L.\u00a0Angew. Chem. Int. Ed.,<\/em>\u00a02015<\/strong>,\u00a054<\/em>, 11754-11759.[This paper was highlighted in numerous journals including ACS Chem Bio, Synthetic Letters and Future Medicinal Chemistry] (doi:\u00a0https:doi.org\/10.1002\/anie.201506085<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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14) \u201cCatalysis by electrons and holes: formal potential scales and preparative organic electrochemistry” Luca, R. O.; Gustafson, J. L.; Maddox, S. M.; Fenwick, A. Q.; Smith, D. C, Organic Chemistry Frontiers\u00a02015<\/strong>,\u00a02<\/em>, 823-848. (doi:\u00a0https:\/\/doi.org\/10.1039\/C5QO00075K<\/a>)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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13) \u201cA Practical Lewis-Base catalyzed electrophilic chlorination of Arenes and Heterocycles\u201dMaddox, S. M.; Nalbandian, C. J.; Smith, D. E.; Gustafson, J. L.\u00a02015<\/strong>\u00a0Organic Letters 17<\/em>, 1042-1045.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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12) \u201cHaloPROTACS: Use of Small Molecule PROTACs to Induce Degradation of HaloTag Fusion Proteins.\u201d Buckley, D. L.; Raina, K.; Darricarrerre, N.; Hines, J.; Gustafson, J. L.; Smith, I. E.; Miah, A. H.; Harling, J. D.; Crews, C. M.\u00a0ACS Chem. Biol.<\/em>\u00a02015,\u00a0<\/strong>10<\/em>, 1831-1837.<\/p>

11) \u00a0\u201cCatalytic\u00a0in vivo<\/em>\u00a0Protein Knockdown by small-molecule PROTACS\u201d Bondeson, D. P.; Mares, A.; Smith, I. E. D.; Ko, E.; Campos, S.; Miah, A. H.; Mulholland, K. E.; Routly, N.; Buckley, D. L.; Gustafson, J. L.; Zinn, N.; Grandi, P.; Shimamura, S.; Bergamini, G.; Faelth-Savitski, M.; Bantscheff, M.; Cox, C.; Gordon, D. A.; Willard, R. R.; Flanagan, J. J.; Casillas, L. N.; Votta, B. J.; den Besten, W.; Famm, K.; Kruidenier, L.; Carter, P. S.; Harling, J. D.; Churcher, I.; Crews, C. M.\u00a0Nature Chem. Bio<\/em>.\u00a02015<\/strong>\u00a011<\/em>, 611-617.<\/p>

10) “Small Molecule Mediated Degradation of the Androgen Receptor Through Hydrophobic Tagging”\u00a0Gustafson, J. L.; Neklesa, T. K.; Cox, C. S.; Roth, A. G.; Buckley. S. L.; Tae, H.-Y.; Sundberg, T. B.; McDonnell, D. P.; Morris, J. D.; Crews, C. M.; Angew. Chem. Int. Ed.\u00a02015<\/strong>,\u00a054<\/em>, 9659-9662.<\/p>

9)\u00a0<\/strong>\u201cSmall Molecule Inhibitors of the Interaction Between the E3 Ligase VHL and HIF1\u03b1\u201d \u00a0Buckley, D. L.;\u00a0Gustafson, J. L.<\/strong>; Van Molle, I.; Roth, A. G.; Tae, H.S.; Gareiss, P.C.; Jorgensen, W. L.; Ciulli, A.; Crews, C. M.\u00a0Angew. Chem. Int. Ed.\u00a0<\/em>2012<\/strong>,\u00a051, 11463-11467<\/em>.<\/p>

8)\u00a0\u201dIdentification of Hydrophobic Tags for the Degradation of Stabilized Proteins.\u201dTae, H. S.; Sundberg, T.; Neklesa, T. K.; Noblin, D. J.:\u00a0Gustafson, J. L.<\/strong>; Roth, A. G.; Raina, K.; Crews, C. M.\u00a0ChemBioChem<\/em>,\u00a02012<\/strong>,\u00a04<\/em>, 538-541.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Publications as a Graduate Student at Yale University<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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7) \u201cSynthesis of Atropisomerically Defined, Highly Substituted Biaryl Scaffolds through Catalytic Enantioselective Bromination and Regioselective Cross-Coupling.\u201d\u00a0Gustafson, J. L.; Lim, D.; Barrett, K.; Miller, S. J.\u00a0Angew. Chem. Int. Ed.\u00a0<\/em>2011<\/strong>,\u00a050<\/em>, 5025-5029.<\/p>

6)\u00a0<\/em>\u201cLinear Free Energy Relationship Analysis of a Catalytic Desymmetrization of a Diarylmethane-Bis(phenol).\u201d \u00a0Gustafson, J. L.; Sigman, M. S.; Miller, S. J.\u00a0Org. Lett.\u00a0<\/em>2010<\/strong>.\u00a012<\/em>, 2794-2797.<\/p>

5) \u201cDynamic Kinetic Resolution of Biaryl Atropisomers via Peptide-Catalyzed Bromination.\u201d\u00a0Gustafson, J. L.; Lim, D.; Miller, S. J.\u00a0Science<\/em>\u00a02010<\/strong>,\u00a0328<\/em>, 1251-1255. \u00a0 [Highlighted in “Better Route To Hard-To-Get Isomers.” Science and Technology section of\u00a0Chemical and Engineering<\/em>\u00a0News, 21 June 2010-issue, page 32.] [Highlighted in Cozzi, P. G.; Emer, E.; Gualandi, A. \u201cAtropselective Organocatalysis\u201d\u00a0Angew Chem. Int. Ed.\u00a0<\/em>2011<\/strong>,\u00a050<\/em>, 3847-3849.]<\/p>

4) \u201cA Case of Remote Asymmetric Induction in the Peptide-Catalyzed Desymmetrization of a Bis(phenol).\u201d Lewis, C. A.; Gustafson, J. L.; Chiu, A.; Balsells, J.; Pollard, D.; Murry, J.; Reamer, R. A.; Hansen, K. B.; Miller, S. J.\u00a0J. Am. Chem. Soc.<\/em>\u00a02008<\/strong>,\u00a0130<\/em>, 16358-16365.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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3) “Bifunctional Catalysis of Alkene Isomerization and its Applications.” Grotjahn, D. B.; Larsen, C, R; Erdogan, G; Gustafson, J. L; Sharma, A.; Nair, R.\u00a0Catal. Org. React<\/em>.\u00a02009<\/strong>,\u00a0123<\/em>, 379-387.<\/p>

2) “A Convenient Method for Regeneration of Free Thiol from a tert-Butyl Thioether.” \u00a0Kragulj, E. J.;\u00a0Gustafson, J. L<\/strong>.; Grotjahn, D. B.\u00a0Synlett<\/em>,\u00a02007<\/strong>, 2851-2854.<\/p>

1) “Extensive Isomerization of Alkenes using a Bifunctional Catalyst: An Alkene Zipper.” Grotjahn, D. B.; Larsen, C. R.;\u00a0Gustafson, J. L.<\/strong>; Nair, R.; Sharma, A.\u00a0J. Am. Chem. Soc.<\/em>\u00a02007<\/strong>,\u00a0129<\/em>, 9592-9593. [see also “Isomerization at a distance.” Science and Technology Concentrates section of\u00a0Chemical and Engineering News<\/em>, 23 July 2007 issue, page 29.]<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Publications as Professor at San Diego State University 44) “CySP3-96 enables scalable, streamlined, and low-cost sample preparation for cysteine chemoproteomic applications” Shikwana, F.; Heydari, B.; Ofori, S.; Truong, C.; Turmon, A.; Darrouj, J.; Holoidovsky, L; Gustafson, J.; Backus, K. ChemRxiv. 2024\u00a0(link) 43) “Targeting the RET tyrosine kinase in neuroblastoma: A […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-50","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/pages\/50","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/comments?post=50"}],"version-history":[{"count":170,"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/pages\/50\/revisions"}],"predecessor-version":[{"id":1675,"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/pages\/50\/revisions\/1675"}],"wp:attachment":[{"href":"https:\/\/gustafsongroup.sdsu.edu\/wordpress\/index.php\/wp-json\/wp\/v2\/media?parent=50"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}