<h1>Reisman, Sarah</h1>
<h2>Article from <a href="https://authors.library.caltech.edu">CaltechAUTHORS</a></h2>
<ul>
<li>Chen, Li-Ming and Reisman, Sarah E. (2024) <a href="https://authors.library.caltech.edu/records/fza0k-nz477">Enantioselective C(sp²)–C(sp³) Bond Construction by Ni Catalysis</a>; Accounts of Chemical Research; Vol. 57; No. 5; 751-762; PMCID PMC10918837; <a href="https://doi.org/10.1021/acs.accounts.3c00775">10.1021/acs.accounts.3c00775</a></li>
<li>Gao, Yang and Jiang, Baiyang, el al. (2024) <a href="https://authors.library.caltech.edu/records/9yt41-rn292">Electrocatalytic Asymmetric Nozaki–Hiyama–Kishi Decarboxylative Coupling: Scope, Applications, and Mechanism</a>; Journal of the American Chemical Society; Vol. 146; No. 7; 4872-4882; <a href="https://doi.org/10.1021/jacs.3c13442">10.1021/jacs.3c13442</a></li>
<li>Raghavan, Priyanka and Haas, Brittany C., el al. (2023) <a href="https://authors.library.caltech.edu/records/ygx5p-w2q53">Dataset Design for Building Models of Chemical Reactivity</a>; ACS Central Science; PMCID PMC10755851; <a href="https://doi.org/10.1021/acscentsci.3c01163">10.1021/acscentsci.3c01163</a></li>
<li>Lam, Pik Hoi and Kerkovius, Jeff K., el al. (2023) <a href="https://authors.library.caltech.edu/records/wg0jz-5bn23">A Pyridine Dearomatization Approach for the Gram Scale Synthesis of (±)-Sparteine</a>; Organic Letters; Vol. 25; No. 46; 8230-8233; PMCID PMC10683365; <a href="https://doi.org/10.1021/acs.orglett.3c03242">10.1021/acs.orglett.3c03242</a></li>
<li>Grünenfelder, Denise C. and Reisman, Sarah E., el al. (2023) <a href="https://authors.library.caltech.edu/records/xhvmh-0bz10">Isolation, biosynthesis, and chemical syntheses of the hasubanan and acutumine alkaloids: A historical perspective</a>; Tetrahedron; 133709; <a href="https://doi.org/10.1016/j.tet.2023.133709">10.1016/j.tet.2023.133709</a></li>
<li>McNicholas, Brendon J. and Tong, Z. Jaron, el al. (2023) <a href="https://authors.library.caltech.edu/records/5v97q-b4c50">Electronic Structures of Nickel(II)-Bis(indanyloxazoline)-dihalide Catalysts: Understanding Ligand Field Contributions That Promote C(sp²)–C(sp³) Cross-Coupling</a>; Inorganic Chemistry; Vol. 62; No. 34; 14010-14027; PMCID PMC10530056; <a href="https://doi.org/10.1021/acs.inorgchem.3c02048">10.1021/acs.inorgchem.3c02048</a></li>
<li>Turro, Raymond F. and Wahlman, Julie L. H., el al. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230710-599244800.28">Mechanistic Investigation of Ni-Catalyzed Reductive Cross-Coupling of Alkenyl and Benzyl Electrophiles</a>; Journal of the American Chemical Society; Vol. 145; No. 27; 14705-14715; PMCID PMC10347553; <a href="https://doi.org/10.1021/jacs.3c02649">10.1021/jacs.3c02649</a></li>
<li>Barbor, Jay P. and Nair, Vaishnavi N., el al. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230725-856879000.13">Development of a Nickel-Catalyzed N–N Coupling for the Synthesis of Hydrazides</a>; Journal of the American Chemical Society; Vol. 145; No. 28; 15071-15077; PMCID PMC10360072; <a href="https://doi.org/10.1021/jacs.3c04834">10.1021/jacs.3c04834</a></li>
<li>Kerkovius, Jeff K. and Wong, Alice R., el al. (2023) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230630-537309000.7">A convergent fragment coupling strategy to access quaternary stereogenic centers</a>; Chemical Science; Vol. 14; No. 16; 4397-4400; PMCID PMC10132171; <a href="https://doi.org/10.1039/d2sc07023e">10.1039/d2sc07023e</a></li>
<li>Lacker, Caitlin R. and DeLano, Travis J., el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20230125-514893900.20">Enantioselective Synthesis of N-Benzylic Heterocycles by Ni/Photoredox Dual Catalysis</a>; Journal of the American Chemical Society; Vol. 144; No. 44; 20190-20195; PMCID PMC10326726; <a href="https://doi.org/10.1021/jacs.2c07917">10.1021/jacs.2c07917</a></li>
<li>Turro, Raymond F. and Brandstätter, Marco, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220721-9036000">Nickel‐Catalyzed Reductive Alkylation of Heteroaryl Imines</a>; Angewandte Chemie International Edition; <a href="https://doi.org/10.1002/anie.202207597">10.1002/anie.202207597</a></li>
<li>Kerkovius, Jeff K. and Stegner, Andrea, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220909-232904000">A Pyridine Dearomatization Approach to the Matrine-Type Lupin Alkaloids</a>; Journal of the American Chemical Society; Vol. 144; No. 35; 15938-15943; PMCID PMC10249042; <a href="https://doi.org/10.1021/jacs.2c06584">10.1021/jacs.2c06584</a></li>
<li>Mendoza, Skyler D. and Rombola, Michael, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220523-165225000">Expanding the Chiral Monoterpene Pool: Enantioselective Diels–Alder Reactions of α-Acyloxy Enones</a>; Organic Letters; Vol. 24; No. 21; 3802-3806; <a href="https://doi.org/10.1021/acs.orglett.2c01343">10.1021/acs.orglett.2c01343</a></li>
<li>Gnaim, Samer and Bauer, Adriano, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20211124-184849879">Cobalt-electrocatalytic HAT for functionalization of unsaturated C–C bonds</a>; Nature; Vol. 605; No. 7911; 687-695; PMCID PMC9206406; <a href="https://doi.org/10.1038/s41586-022-04595-3">10.1038/s41586-022-04595-3</a></li>
<li>Holman, Karli R. and Stanko, Allison M., el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220419-936123000">Synthesis of Noraugustamine and Development of an Oxidative Heck/Aza-Wacker Cascade Cyclization</a>; Organic Letters; Vol. 24; No. 16; 3019-3023; <a href="https://doi.org/10.1021/acs.orglett.2c00948">10.1021/acs.orglett.2c00948</a></li>
<li>Grünenfelder, Denise C. and Navarro, Raul, el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20220204-679540000">Enantioselective Synthesis of (−)-10-Hydroxyacutuminine</a>; Angewandte Chemie International Edition; Vol. 61; No. 16; Art. No. e202117480; <a href="https://doi.org/10.1002/anie.202117480">10.1002/anie.202117480</a></li>
<li>Dibrell, Sara E. and Holman, Karli R., el al. (2022) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20211220-494395000">Plugging the Leak: Empowering Women in Organic Chemistry</a>; Angewandte Chemie International Edition; Vol. 61; No. 5; Art. No. e202111765; <a href="https://doi.org/10.1002/anie.202111765">10.1002/anie.202111765</a></li>
<li>Wong, Alice R. and Fastuca, Nicholas J., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210513-103036703">Total Syntheses of the C₁₉ Diterpenoid Alkaloids (–)-Talatisamine, (–)-Liljestrandisine, and (–)-Liljestrandinine by a Fragment Coupling Approach</a>; ACS Central Science; Vol. 7; No. 8; 1311-1316; PMCID PMC8393236; <a href="https://doi.org/10.1021/acscentsci.1c00540">10.1021/acscentsci.1c00540</a></li>
<li>Holman, K. R. and Stanko, A. M., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210527-093457647">Palladium-catalyzed cascade cyclizations involving C–C and C–X bond formation: strategic applications in natural product synthesis</a>; Chemical Society Reviews; Vol. 50; No. 14; 7891-7908; <a href="https://doi.org/10.1039/d0cs01385d">10.1039/d0cs01385d</a></li>
<li>Gao, Yang and Hill, David E., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210625-220045705">Electrochemical Nozaki–Hiyama–Kishi Coupling: Scope, Applications, and Mechanism</a>; Journal of the American Chemical Society; Vol. 143; No. 25; 9478-9488; PMCID PMC8720499; <a href="https://doi.org/10.1021/jacs.1c03007">10.1021/jacs.1c03007</a></li>
<li>DeLano, Travis J. and Dibrell, Sara E., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210113-152642442">Nickel-catalyzed asymmetric reductive cross-coupling of α-chloroesters with (hetero)aryl iodides</a>; Chemical Science; Vol. 12; No. 22; 7758-7762; PMCID PMC8188512; <a href="https://doi.org/10.1039/d1sc00822f">10.1039/d1sc00822f</a></li>
<li>Reisman, Sarah E. and Maimone, Thomas J. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210423-164904801">Total Synthesis of Complex Natural Products: More Than a Race for Molecular Summits</a>; Accounts of Chemical Research; Vol. 54; No. 8; 1815-1816; <a href="https://doi.org/10.1021/acs.accounts.1c00184">10.1021/acs.accounts.1c00184</a></li>
<li>Nakayama, Yasuaki and Maser, Michael R., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210202-123615131">Total Synthesis of Ritterazine B</a>; Journal of the American Chemical Society; Vol. 143; No. 11; 4187-4192; <a href="https://doi.org/10.1021/jacs.1c01372">10.1021/jacs.1c01372</a></li>
<li>Dibrell, Sara E. and Tao, Yujia, el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210224-121416493">Synthesis of Complex Diterpenes: Strategies Guided by Oxidation Pattern Analysis</a>; Accounts of Chemical Research; Vol. 54; No. 6; 1360-1373; PMCID PMC9169581; <a href="https://doi.org/10.1021/acs.accounts.0c00858">10.1021/acs.accounts.0c00858</a></li>
<li>Maser, Michael R. and Cui, Alexander Y., el al. (2021) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20201015-152733539">Multilabel Classification Models for the Prediction of Cross-Coupling Reaction Conditions</a>; Journal of Chemical Information and Modeling; Vol. 61; No. 1; 156-166; <a href="https://doi.org/10.1021/acs.jcim.0c01234">10.1021/acs.jcim.0c01234</a></li>
<li>Cowper, Nicholas G. W. and Hesse, Matthew J., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20201015-152733817">A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core</a>; Chemical Science; Vol. 11; No. 43; 11897-11901; PMCID PMC8162951; <a href="https://doi.org/10.1039/d0sc04802j">10.1039/d0sc04802j</a></li>
<li>Blom, Annet E. M. and Su, Justin Y., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200924-152452617">Synthesis and Biological Evaluation of Pyrroloindolines as Positive Allosteric Modulators of the α1β2γ2 GABA_A Receptor</a>; ACS Medicinal Chemistry Letters; Vol. 11; No. 11; 2204-2211; PMCID PMC7667864; <a href="https://doi.org/10.1021/acsmedchemlett.0c00340">10.1021/acsmedchemlett.0c00340</a></li>
<li>Fastuca, Nicholas J. and Wong, Alice R., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20210125-140300975">Asymmetric Michael Addition of Dimethyl Malonate to 2 Cyclopenten-1-one Catalyzed by a Heterobimetallic Complex</a>; Organic Syntheses; Vol. 97; 327-338; PMCID PMC9128456; <a href="https://doi.org/10.15227/orgsyn.097.0327">10.15227/orgsyn.097.0327</a></li>
<li>Reisman, Sarah E. and Sarpong, Richmond, el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200810-143641171">Organic Chemistry: A Call to Action for Diversity and Inclusion</a>; ACS Central Science; Vol. 6; No. 8; 1241-1247; PMCID PMC7453412; <a href="https://doi.org/10.1021/acscentsci.0c01027">10.1021/acscentsci.0c01027</a></li>
<li>Reisman, Sarah E. and Sarpong, Richmond, el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200810-142124575">Organic Chemistry: A Call to Action for Diversity and Inclusion</a>; Organometallics; Vol. 39; No. 16; 2931-2936; <a href="https://doi.org/10.1021/acs.organomet.0c00519">10.1021/acs.organomet.0c00519</a></li>
<li>Reisman, Sarah E. and Sarpong, Richmond, el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200810-150113613">Organic Chemistry: A Call to Action for Diversity and Inclusion</a>; Organic Letters; Vol. 22; No. 16; 6223-6228; <a href="https://doi.org/10.1021/acs.orglett.0c02559">10.1021/acs.orglett.0c02559</a></li>
<li>Reisman, Sarah E. and Sarpong, Richmond, el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200810-134855232">Organic Chemistry: A Call to Action for Diversity and Inclusion</a>; Journal of Organic Chemistry; Vol. 85; No. 16; 10287-10292; <a href="https://doi.org/10.1021/acs.joc.0c01607">10.1021/acs.joc.0c01607</a></li>
<li>Hofstra, Julie L. and DeLano, Travis J., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20201109-125642953">Synthesis of Chiral Bisoxazoline Ligands: (3aR,3a'R,8aS,8a'S)-2,2'-(cyclopropane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole)</a>; Organic Syntheses; Vol. 97; 172-188; PMCID PMC8294164; <a href="https://doi.org/10.15227/orgsyn.097.0172">10.15227/orgsyn.097.0172</a></li>
<li>Poremba, Kelsey E. and Dibrell, Sara E., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200624-154304037">Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions</a>; ACS Catalysis; Vol. 10; No. 15; 8237-8246; PMCID PMC7470226; <a href="https://doi.org/10.1021/acscatal.0c01842">10.1021/acscatal.0c01842</a></li>
<li>Wittmann, Bruce J. and Knight, Anders M., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200608-115355402">Diversity-Oriented Enzymatic Synthesis of Cyclopropane Building Blocks</a>; ACS Catalysis; Vol. 10; No. 13; 7112-7116; PMCID PMC7709968; <a href="https://doi.org/10.1021/acscatal.0c01888">10.1021/acscatal.0c01888</a></li>
<li>Dibrell, Sara E. and Maser, Michael R., el al. (2020) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20200319-125552181">SeO₂-Mediated Oxidative Transposition of Pauson–Khand Products</a>; Journal of the American Chemical Society; Vol. 142; No. 14; 6483-6487; <a href="https://doi.org/10.1021/jacs.9b13818">10.1021/jacs.9b13818</a></li>
<li>Hofstra, Julie L. and Poremba, Kelsey E., el al. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190805-134105383">Nickel-Catalyzed Conversion of Enol Triflates into Alkenyl Halides</a>; Angewandte Chemie International Edition; Vol. 58; No. 42; 14901-14905; PMCID PMC7179072; <a href="https://doi.org/10.1002/anie.201906815">10.1002/anie.201906815</a></li>
<li>Han, Arthur and Tao, Yujia, el al. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190610-080930538">A 16-step synthesis of the isoryanodane diterpene (+)-perseanol</a>; Nature; Vol. 573; No. 7775; 563-567; PMCID PMC7123484; <a href="https://doi.org/10.1038/s41586-019-1580-x">10.1038/s41586-019-1580-x</a></li>
<li>DeLano, Travis J. and Reisman, Sarah E. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190625-112222475">Enantioselective Electroreductive Coupling of Alkenyl and Benzyl Halides via Nickel Catalysis</a>; ACS Catalysis; Vol. 9; No. 8; 6751-6754; PMCID PMC7190267; <a href="https://doi.org/10.1021/acscatal.9b01785">10.1021/acscatal.9b01785</a></li>
<li>Beck, Jordan C. and Lacker, Caitlin R., el al. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190104-074958444">A modular approach to prepare enantioenriched cyclobutanes: synthesis of (+)-rumphellaone A</a>; Chemical Science; Vol. 10; No. 8; 2315-2319; PMCID PMC6385545; <a href="https://doi.org/10.1039/c8sc05444d">10.1039/c8sc05444d</a></li>
<li>Carreira, Erick M. and Brimble, Margaret, el al. (2019) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20190124-111248679">Organic Letters 2.0: A New Beginning</a>; Organic Letters; Vol. 21; No. 1; 1-4; <a href="https://doi.org/10.1021/acs.orglett.8b03964">10.1021/acs.orglett.8b03964</a></li>
<li>Su, Justin Y. and Grünenfelder, Denise C., el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20180731-110815223">Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides</a>; Organic Letters; Vol. 20; No. 16; 4912-4916; <a href="https://doi.org/10.1021/acs.orglett.8b02045">10.1021/acs.orglett.8b02045</a></li>
<li>Xu, Chen and Han, Arthur, el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20180613-100330914">An Oxidative Dearomatization Approach To Prepare the Pentacyclic Core of Ryanodol</a>; Organic Letters; Vol. 20; No. 13; 3793-3796; PMCID PMC6103443; <a href="https://doi.org/10.1021/acs.orglett.8b01387">10.1021/acs.orglett.8b01387</a></li>
<li>Chapman, Lauren M. and Beck, Jordan C., el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20180507-092121998">Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B</a>; Journal of Organic Chemistry; Vol. 83; No. 11; 6066-6085; PMCID PMC5990278; <a href="https://doi.org/10.1021/acs.joc.8b00728">10.1021/acs.joc.8b00728</a></li>
<li>Farney, Elliot P. and Feng, Sean S., el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20180112-131323403">Total Synthesis of (+)-Pleuromutilin</a>; Journal of the American Chemical Society; Vol. 140; No. 4; 1267-1270; PMCID PMC5988231; <a href="https://doi.org/10.1021/jacs.7b13260">10.1021/jacs.7b13260</a></li>
<li>Hofstra, Julie L. and Cherney, Alan H., el al. (2018) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20171205-112031343">Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling</a>; Journal of the American Chemical Society; Vol. 140; No. 1; 139-142; PMCID PMC5851001; <a href="https://doi.org/10.1021/jacs.7b11707">10.1021/jacs.7b11707</a></li>
<li>Poremba, Kelsey E. and Kadunce, Nathaniel T., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170414-064225830">Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes</a>; Journal of the American Chemical Society; Vol. 139; No. 16; 5684-5687; PMCID PMC5851002; <a href="https://doi.org/10.1021/jacs.7b01705">10.1021/jacs.7b01705</a></li>
<li>Xu, Chen and Han, Arthur, el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170310-084018084">Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine</a>; ACS Central Science; Vol. 3; No. 4; 278-282; PMCID PMC5409222; <a href="https://doi.org/10.1021/acscentsci.6b00361">10.1021/acscentsci.6b00361</a></li>
<li>Suzuki, Naoyuki and Hofstra, Julie L., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170405-103159884">Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides</a>; Organic Letters; Vol. 19; No. 8; 2150-2153; PMCID PMC5868419; <a href="https://doi.org/10.1021/acs.orglett.7b00793">10.1021/acs.orglett.7b00793</a></li>
<li>Wang, Haoxuan and Regan, Clinton J., el al. (2017) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20170329-093225716">Enantioselective Synthesis of (−)-Acetylapoaranotin</a>; Organic Letters; Vol. 19; No. 7; 1698-1701; PMCID PMC5387676; <a href="https://doi.org/10.1021/acs.orglett.7b00418">10.1021/acs.orglett.7b00418</a></li>
<li>Chuang, Kangway V. and Kieffer, Madeleine E., el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160912-094332366">A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans</a>; Organic Letters; Vol. 18; No. 18; 4750-4753; PMCID PMC5505074; <a href="https://doi.org/10.1021/acs.orglett.6b02477">10.1021/acs.orglett.6b02477</a></li>
<li>Chuang, Kangway V. and Xu, Chen, el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160630-153826956">A 15-step synthesis of (+)-ryanodol</a>; Science; Vol. 353; No. 6302; 912-915; PMCID PMC5505075; <a href="https://doi.org/10.1126/science.aag1028">10.1126/science.aag1028</a></li>
<li>Chapman, Lauren M. and Beck, Jordan C., el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160815-142455841">Enantioselective Total Synthesis of (+)-Psiguadial B</a>; Journal of the American Chemical Society; Vol. 138; No. 31; 9803-9806; <a href="https://doi.org/10.1021/jacs.6b07229">10.1021/jacs.6b07229</a></li>
<li>Daniels, Blake E. and Ni, Jane, el al. (2016) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20160208-143917247">Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction</a>; Angewandte Chemie International Edition; Vol. 55; No. 10; 3398-3402; PMCID PMC4843768; <a href="https://doi.org/10.1002/anie.201510972">10.1002/anie.201510972</a></li>
<li>Cherney, Alan H. and Kadunce, Nathaniel T., el al. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150819-143512446">Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C–C Bonds</a>; Chemical Reviews; Vol. 115; No. 17; 9587-9652; PMCID PMC4566132; <a href="https://doi.org/10.1021/acs.chemrev.5b00162">10.1021/acs.chemrev.5b00162</a></li>
<li>Kadunce, Nathaniel T. and Reisman, Sarah E. (2015) <a href="https://resolver.caltech.edu/CaltechAUTHORS:20150917-141844097">Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles</a>; Journal of the American Chemical Society; Vol. 137; No. 33; 10480-10483; PMCID PMC5066588; <a href="https://doi.org/10.1021/jacs.5b06466">10.1021/jacs.5b06466</a></li>
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