<h1>Fu, Gregory</h1>
<h2>Article from <a href="https://authors.library.caltech.edu">CaltechAUTHORS</a></h2>
<ul>
<li>Hossain, Asik and Anderson, Robert L., el al. (2024) <a href="https://authors.library.caltech.edu/records/y9zc0-fgm21">Nickel-Catalyzed Enantioconvergent and Diastereoselective Allenylation of Alkyl Electrophiles: Simultaneous Control of Central and Axial Chirality</a>; Journal of the American Chemical Society; Vol. 146; No. 11; 7173-7177; PMCID PMC11003353; <a href="https://doi.org/10.1021/jacs.4c00593">10.1021/jacs.4c00593</a></li>
<li>Wang, Zhuo-Yan and Freas, Dylan J., el al. (2023) <a href="https://authors.library.caltech.edu/records/qkc4v-vzc32">Phosphine Catalysis of the Fluorination of Unactivated Tertiary Alkyl Chlorides under Mild and Convenient Conditions</a>; Journal of the American Chemical Society; Vol. 145; No. 46; 25093-25097; PMCID PMC10942731; <a href="https://doi.org/10.1021/jacs.3c11042">10.1021/jacs.3c11042</a></li>
<li>Tong, Xiaoyu and Yang, Ze‐Peng, el al. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230725-746869000.33">Iron‐Catalyzed Reductive Cross‐Coupling of Alkyl Electrophiles with Olefins</a>; Angewandte Chemie International Edition; Art. No. e202306663; PMCID PMC10528270; <a href="https://doi.org/10.1002/anie.202306663">10.1002/anie.202306663</a></li>
<li>Chen, Caiyou and Fu, Gregory C. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230615-812791000.10">Copper-catalysed enantioconvergent alkylation of oxygen nucleophiles</a>; Nature; Vol. 618; No. 7964; 301-307; PMCID PMC10986234; <a href="https://doi.org/10.1038/s41586-023-06001-y">10.1038/s41586-023-06001-y</a></li>
<li>Zuccarello, Giuseppe and Batiste, Suzanne M., el al. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230314-844891400.19">Enantioselective Synthesis of α-Aminoboronic Acid Derivatives via Copper-Catalyzed N-Alkylation</a>; Journal of the American Chemical Society; Vol. 145; No. 6; 3330-3334; PMCID PMC10079214; <a href="https://doi.org/10.1021/jacs.3c00038">10.1021/jacs.3c00038</a></li>
<li>Tong, Xiaoyu and Schneck, Felix, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220805-758034000">Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles</a>; Journal of the American Chemical Society; Vol. 144; No. 32; 14856-14863; PMCID PMC10079215; <a href="https://doi.org/10.1021/jacs.2c06154">10.1021/jacs.2c06154</a></li>
<li>Cho, Hyungdo and Suematsu, Hidehiro, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220307-188438000">Photoinduced, Copper-Catalyzed Enantioconvergent Alkylations of Anilines by Racemic Tertiary Electrophiles: Synthesis and Mechanism</a>; Journal of the American Chemical Society; Vol. 144; No. 10; 4550-4558; PMCID PMC9239302; <a href="https://doi.org/10.1021/jacs.1c12749">10.1021/jacs.1c12749</a></li>
<li>Lee, Heejun and Ahn, Jun Myun, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220216-527740512">Investigation of the C–N Bond-Forming Step in a Photoinduced, Copper-Catalyzed Enantioconvergent N–Alkylation: Characterization and Application of a Stabilized Organic Radical as a Mechanistic Probe</a>; Journal of the American Chemical Society; Vol. 144; No. 9; 4114-4123; PMCID PMC9269863; <a href="https://doi.org/10.1021/jacs.1c13151">10.1021/jacs.1c13151</a></li>
<li>Chen, Caiyou and Peters, Jonas C., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210527-133944938">Photoinduced copper-catalysed asymmetric amidation via ligand cooperativity</a>; Nature; Vol. 596; No. 7871; 250-256; PMCID PMC8363576; <a href="https://doi.org/10.1038/s41586-021-03730-w">10.1038/s41586-021-03730-w</a></li>
<li>Yang, Ze-Peng and Freas, Dylan J., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210604-111535270">Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling</a>; Journal of the American Chemical Society; Vol. 143; No. 23; 8614-8618; PMCID PMC8351905; <a href="https://doi.org/10.1021/jacs.1c03903">10.1021/jacs.1c03903</a></li>
<li>Wang, Zhaobin and Yang, Ze-Peng, el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210111-120204779">Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides</a>; Nature Chemistry; Vol. 13; No. 3; 236-242; <a href="https://doi.org/10.1038/s41557-020-00609-7">10.1038/s41557-020-00609-7</a></li>
<li>Yang, Ze-Peng and Freas, Dylan J., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210211-151616006">The Asymmetric Synthesis of Amines via Nickel-Catalyzed Enantioconvergent Substitution Reactions</a>; Journal of the American Chemical Society; Vol. 143; No. 7; 2930-2937; PMCID PMC8336453; <a href="https://doi.org/10.1021/jacs.0c13034">10.1021/jacs.0c13034</a></li>
<li>Yang, Ze-Peng and Fu, Gregory C. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200316-151135011">Convergent Catalytic Asymmetric Synthesis of Esters of Chiral Dialkyl Carbinols</a>; Journal of the American Chemical Society; Vol. 142; No. 12; 5870-5875; PMCID PMC7580270; <a href="https://doi.org/10.1021/jacs.0c01324">10.1021/jacs.0c01324</a></li>
<li>Huo, Haohua and Gorsline, Bradley J., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200130-135407173">Catalyst-controlled doubly enantioconvergent coupling of racemic alkyl nucleophiles and electrophiles</a>; Science; Vol. 367; No. 6477; 559-564; PMCID PMC7566878; <a href="https://doi.org/10.1126/science.aaz3855">10.1126/science.aaz3855</a></li>
<li>Yin, Haolin and Fu, Gregory C. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190910-110659740">Mechanistic Investigation of Enantioconvergent Kumada Reactions of Racemic α-Bromoketones Catalyzed by a Nickel/Bis(oxazoline) Complex</a>; Journal of the American Chemical Society; Vol. 141; No. 38; 15433-15440; PMCID PMC7075318; <a href="https://doi.org/10.1021/jacs.9b08185">10.1021/jacs.9b08185</a></li>
<li>Bartoszewicz, Agnieszka and Matier, Carson D., el al. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190909-093503148">Enantioconvergent Alkylations of Amines by Alkyl Electrophiles: Copper-Catalyzed Nucleophilic Substitutions of Racemic α-Halolactams by Indoles</a>; Journal of the American Chemical Society; Vol. 141; No. 37; 14864-14869; PMCID PMC7055584; <a href="https://doi.org/10.1021/jacs.9b07875">10.1021/jacs.9b07875</a></li>
<li>Masuda, Yusuke and Fu, Gregory C. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200210-082805136">Synthesis of Chiral Diamine Ligands for Nickel-catalyzed Asymmetric Cross-couplings of Alkylchloroboronate Esters with Alkylzincs: (1R,2R)-N,N'-Dimethyl-1,2-bis(2-methylphenyl)-1,2-diaminoethane</a>; Organic Syntheses; Vol. 96; 245-257; PMCID PMC7064032; <a href="https://doi.org/10.15227/orgsyn.096.0245">10.15227/orgsyn.096.0245</a></li>
<li>Fu, Gregory C. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190122-084528318">Enantioconvergent Cross−Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes</a>; Angewandte Chemie International Edition; Vol. 58; No. 11; 3571-3574; PMCID PMC6399024; <a href="https://doi.org/10.1002/anie.201814208">10.1002/anie.201814208</a></li>
<li>He, Jian and Chen, Caiyou, el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20181031-131746669">Visible-Light-Induced, Copper-Catalyzed Three-Component Coupling of Alkyl Halides, Olefins, and Trifluoromethylthiolate to Generate Trifluoromethyl Thioethers</a>; ACS Catalysis; Vol. 8; No. 12; 11741-11748; PMCID PMC6687088; <a href="https://doi.org/10.1021/acscatal.8b04094">10.1021/acscatal.8b04094</a></li>
<li>Wang, Zhaobin and Yin, Haolin, el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20181002-161720440">Catalytic Enantioconvergent Couplings of Secondary and Tertiary Electrophiles with Olefins</a>; Nature; Vol. 563; No. 7731; 379-383; PMCID PMC6296363; <a href="https://doi.org/10.1038/s41586-018-0669-y">10.1038/s41586-018-0669-y</a></li>
<li>Wang, Zhaobin and Bachman, Shoshana, el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20180806-125754691">Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles</a>; Angewandte Chemie International Edition; Vol. 57; No. 44; 14529-14532; PMCID PMC6200647; <a href="https://doi.org/10.1002/anie.201806015">10.1002/anie.201806015</a></li>
<li>Matier, Carson D. and Schwaben, Jonas, el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20171128-135738544">Copper-Catalyzed Alkylation of Aliphatic Amines Induced by Visible Light</a>; Journal of the American Chemical Society; Vol. 139; No. 49; 17707-17710; PMCID PMC6044445; <a href="https://doi.org/10.1021/jacs.7b09582">10.1021/jacs.7b09582</a></li>
<li>Ahn, Jun Myun and Peters, Jonas C., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20171205-074829551">Design of a Photoredox Catalyst that Enables the Direct Synthesis of Carbamate-Protected Primary Amines via Photoinduced, Copper-Catalyzed N-Alkylation Reactions of Unactivated Secondary Halides</a>; Journal of the American Chemical Society; Vol. 139; No. 49; 18101-18106; PMCID PMC6039098; <a href="https://doi.org/10.1021/jacs.7b10907">10.1021/jacs.7b10907</a></li>
<li>Ahn, Jun Myun and Ratani, Tanvi S., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170818-105931485">Photoinduced, Copper-Catalyzed Alkylation of Amines: A Mechanistic Study of the Cross-Coupling of Carbazole with Alkyl Bromides</a>; Journal of the American Chemical Society; Vol. 139; No. 36; 12716-12723; PMCID PMC5685493; <a href="https://doi.org/10.1021/jacs.7b07052">10.1021/jacs.7b07052</a></li>
<li>Zhao, Wei and Wurz, Ryan P., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170828-124616088">Photoinduced, Copper-Catalyzed Decarboxylative C–N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement</a>; Journal of the American Chemical Society; Vol. 139; No. 35; 12153-12156; PMCID PMC5624330; <a href="https://doi.org/10.1021/jacs.7b07546">10.1021/jacs.7b07546</a></li>
<li>Fu, Gregory C. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170613-111718684">Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to S_N1 and S_N2 Processes</a>; ACS Central Science; Vol. 3; No. 7; 692-700; PMCID PMC5532721; <a href="https://doi.org/10.1021/acscentsci.7b00212">10.1021/acscentsci.7b00212</a></li>
<li>Mu, Xin and Shibata, Yu, el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170419-135029412">Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling</a>; Angewandte Chemie International Edition; Vol. 56; No. 21; 5821-5824; PMCID PMC5595219; <a href="https://doi.org/10.1002/anie.201702402">10.1002/anie.201702402</a></li>
<li>Choi, Junwon and Fu, Gregory C. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170413-145407242">Transition metal–catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry</a>; Science; Vol. 356; No. 6334; Art. No. eaaf7230; PMCID PMC5611817; <a href="https://doi.org/10.1126/science.aaf7230">10.1126/science.aaf7230</a></li>
<li>Kalek, Marcin and Fu, Gregory C. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170313-071527443">Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species</a>; Journal of the American Chemical Society; Vol. 139; No. 11; 4225-4229; PMCID PMC5486213; <a href="https://doi.org/10.1021/jacs.7b01826">10.1021/jacs.7b01826</a></li>
<li>Schmidt, Jens and Choi, Junwon, el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20161212-113915733">A general, modular method for the catalytic asymmetric synthesis of alkylboronate esters</a>; Science; Vol. 354; No. 6317; 1265-1269; PMCID PMC5619240; <a href="https://doi.org/10.1126/science.aai8611">10.1126/science.aai8611</a></li>
<li>Ziegler, Daniel T. and Fu, Gregory C. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160919-131412998">Catalytic Enantioselective Carbon–Oxygen Bond Formation: Phosphine-Catalyzed Synthesis of Benzylic Ethers via the Oxidation of Benzylic C–H Bonds</a>; Journal of the American Chemical Society; Vol. 138; No. 37; 12069-12072; PMCID PMC5065328; <a href="https://doi.org/10.1021/jacs.6b08486">10.1021/jacs.6b08486</a></li>
<li>Chu, Crystal K. and Liang, Yufan, el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160524-081446502">Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles</a>; Journal of the American Chemical Society; Vol. 138; No. 20; 6404-6407; PMCID PMC5031417; <a href="https://doi.org/10.1021/jacs.6b03465">10.1021/jacs.6b03465</a></li>
<li>Johnson, Miles W. and Hannoun, Kareem I., el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160323-130838018">A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide</a>; Chemical Science; Vol. 7; 4091-4100; PMCID PMC5201211; <a href="https://doi.org/10.1039/c5sc04709a">10.1039/c5sc04709a</a></li>
<li>Kainz, Quirin M. and Matier, Carson D., el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160216-092106614">Asymmetric copper-catalyzed C-N cross-couplings induced by visible light</a>; Science; Vol. 351; No. 6274; 681-684; PMCID PMC4770572; <a href="https://doi.org/10.1126/science.aad8313">10.1126/science.aad8313</a></li>
<li>Zuo, Zhiwei and Cong, Huan, el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160216-091421574">Enantioselective Decarboxylative Arylation of α-Amino Acids via the Merger of Photoredox and Nickel Catalysis</a>; Journal of the American Chemical Society; Vol. 138; No. 6; 1832-1835; PMCID PMC4862596; <a href="https://doi.org/10.1021/jacs.5b13211">10.1021/jacs.5b13211</a></li>
<li>Ratani, Tanvi S. and Bachman, Shoshana, el al. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20151027-113729482">Photoinduced, Copper-Catalyzed Carbon–Carbon Bond Formation with Alkyl Electrophiles: Cyanation of Unactivated Secondary Alkyl Chlorides at Room Temperature</a>; Journal of the American Chemical Society; Vol. 137; No. 43; 13902-13907; PMCID PMC4666296; <a href="https://doi.org/10.1021/jacs.5b08452">10.1021/jacs.5b08452</a></li>
<li>Liang, Yufan and Fu, Gregory C. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150728-091314884">Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF_3 and an Alkyl Group</a>; Journal of the American Chemical Society; Vol. 137; No. 30; 9523-9526; PMCID PMC4610818; <a href="https://doi.org/10.1021/jacs.5b04725">10.1021/jacs.5b04725</a></li>
<li>Kalek, Marcin and Fu, Gregory C. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150728-084201151">Phosphine-Catalyzed Doubly Stereoconvergent γ-Additions of Racemic Heterocycles to Racemic Allenoates: The Catalytic Enantioselective Synthesis of Protected α,α-Disubstituted α-Amino Acid Derivatives</a>; Journal of the American Chemical Society; Vol. 137; No. 29; 9438-9442; PMCID PMC4577964; <a href="https://doi.org/10.1021/jacs.5b05528">10.1021/jacs.5b05528</a></li>
<li>Liang, Yufan and Fu, Gregory C. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150617-075445770">Nickel-Catalyzed Alkyl–Alkyl Cross-Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent</a>; Angewandte Chemie International Edition; Vol. 54; No. 31; 9047-9051; PMCID PMC4521909; <a href="https://doi.org/10.1002/anie.201503297">10.1002/anie.201503297</a></li>
<li>Lee, Sarah Yunmi and Fujiwara, Yuji, el al. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150406-090131028">Phosphine-Catalyzed Enantioselective Intramolecular [3+2] Annulations To Generate Fused Ring Systems</a>; Journal of the American Chemical Society; Vol. 137; No. 13; 4587-4591; PMCID PMC4433041; <a href="https://doi.org/10.1021/jacs.5b01985">10.1021/jacs.5b01985</a></li>
<li>Kramer, Søren and Fu, Gregory C. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150323-103746266">Use of a New Spirophosphine To Achieve Catalytic Enantioselective [4 + 1] Annulations of Amines with Allenes To Generate Dihydropyrroles</a>; Journal of the American Chemical Society; Vol. 137; No. 11; 3803-3806; PMCID PMC4433051; <a href="https://doi.org/10.1021/jacs.5b01944">10.1021/jacs.5b01944</a></li>
<li>Fu, Gregory C. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150422-145402543">Photoinduced, copper-catalyzed coupling reaction</a>; Abstracts of Papers of the American Chemical Society; Vol. 249; BMGT-9</li>
<li>Schley, Nathan D. and Fu, Gregory C. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20141125-080958357">Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation</a>; Journal of the American Chemical Society; Vol. 136; No. 47; 16588-16593; PMCID PMC4277758; <a href="https://doi.org/10.1021/ja508718m">10.1021/ja508718m</a></li>
<li>Ziegler, Daniel T. and Riesgo, Lorena, el al. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20141015-153508295">Biphenyl-Derived Phosphepines as Chiral Nucleophilic Catalysts: Enantioselective [4+1] Annulations To Form Functionalized Cyclopentenes</a>; Angewandte Chemie International Edition; Vol. 53; No. 48; 13183-13187; PMCID PMC4433032; <a href="https://doi.org/10.1002/anie.201405854">10.1002/anie.201405854</a></li>
<li>Choi, Junwon and Martín-Gago, Pablo, el al. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140825-090042780">Stereoconvergent Arylations and Alkenylations of Unactivated Alkyl Electrophiles: Catalytic Enantioselective Synthesis of Secondary Sulfonamides and Sulfones</a>; Journal of the American Chemical Society; Vol. 136; No. 34; 12161-12165; PMCID PMC4151784; <a href="https://doi.org/10.1021/ja506885s">10.1021/ja506885s</a></li>
<li>Tan, Yichen and Muñoz-Molina, José María, el al. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140710-132652083">Oxygen nucleophiles as reaction partners in photoinduced, copper-catalyzed cross-couplings: O-arylations of phenols at room temperature</a>; Chemical Science; Vol. 5; No. 7; 2831-2835; <a href="https://doi.org/10.1039/c4sc00368c">10.1039/c4sc00368c</a></li>
<li>Lee, Sarah Yunmi and Neufeind, Stefan, el al. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140616-085001666">Enantioselective Nucleophile-Catalyzed Synthesis of Tertiary Alkyl Fluorides via the α‑Fluorination of Ketenes: Synthetic and Mechanistic Studies</a>; Journal of the American Chemical Society; PMCID PMC4091276; <a href="https://doi.org/10.1021/ja5044209">10.1021/ja5044209</a></li>
<li>Liang, Yufan and Fu, Gregory C. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140408-083523386">Catalytic Asymmetric Synthesis of Tertiary Alkyl Fluorides: Negishi Cross-Couplings of Racemic α,α-Dihaloketones</a>; Journal of the American Chemical Society; Vol. 136; No. 14; 5520-5524; PMCID PMC4004247; <a href="https://doi.org/10.1021/ja501815p">10.1021/ja501815p</a></li>
<li>Cong, Huan and Fu, Gregory C. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140304-084532734">Catalytic Enantioselective Cyclization/Cross-Coupling with Alkyl Electrophiles</a>; Journal of the American Chemical Society; Vol. 136; No. 10; 3788-3791; PMCID PMC3985453; <a href="https://doi.org/10.1021/ja500706v">10.1021/ja500706v</a></li>
<li>Do, Hien-Quang and Bachman, Shoshana, el al. (2014) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20140127-095430890">Photoinduced, Copper-Catalyzed Alkylation of Amides with Unactivated Secondary Alkyl Halides at Room Temperature</a>; Journal of the American Chemical Society; Vol. 136; No. 5; 2162-2167; <a href="https://doi.org/10.1021/ja4126609">10.1021/ja4126609</a></li>
<li>Do, Hien-Quang and Chandrashekar, E. R. R., el al. (2013) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20131205-082734303">Nickel/Bis(oxazoline)-Catalyzed Asymmetric Negishi Arylations of Racemic Secondary Benzylic Electrophiles to Generate Enantioenriched 1,1-Diarylalkanes</a>; Journal of the American Chemical Society; Vol. 135; No. 44; 16288-16291; PMCID PMC3869004; <a href="https://doi.org/10.1021/ja408561b">10.1021/ja408561b</a></li>
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