Reisman, Sarah E

(orcid 0000-0001-8244-9300)

Combined from CaltechAUTHORS

• Mendoza, Skyler D.; Rombola, Michael et al. (2022) Expanding the Chiral Monoterpene Pool: Enantioselective Diels–Alder Reactions of α-Acyloxy Enones Organic Letters; Vol. 24; No. 21; https://doi.org/10.1021/acs.orglett.2c01343

• Kerkovius, Jeff K.; Stegner, Andrea et al. (2022) A Pyridine Dearomatization Approach to the Matrine-type Lupin Alkaloids https://doi.org/10.26434/chemrxiv-2022-0v94t

• Gnaim, Samer; Bauer, Adriano et al. (2022) Cobalt-electrocatalytic HAT for functionalization of unsaturated C–C bonds Nature; Vol. 605; No. 7911; https://doi.org/10.1038/s41586-022-04595-3

• Holman, Karli R.; Stanko, Allison M. et al. (2022) Synthesis of Noraugustamine and Development of an Oxidative Heck/Aza-Wacker Cascade Cyclization Organic Letters; Vol. 24; No. 16; https://doi.org/10.1021/acs.orglett.2c00948

• Grünenfelder, Denise C.; Navarro, Raul et al. (2022) Enantioselective Synthesis of (−)-10-Hydroxyacutuminine Angewandte Chemie International Edition; Vol. 61; No. 16; https://doi.org/10.1002/anie.202117480

• Dibrell, Sara E.; Holman, Karli R. et al. (2022) Plugging the Leak: Empowering Women in Organic Chemistry Angewandte Chemie International Edition; Vol. 61; No. 5; In: Empowering Women in Organic Chemistry (EWOC), 24-25 June 2021, Online https://doi.org/10.1002/anie.202111765

• Wong, Alice R.; Fastuca, Nicholas J. et al. (2021) Total Syntheses of the C₁₉ Diterpenoid Alkaloids (–)-Talatisamine, (–)-Liljestrandisine, and (–)-Liljestrandinine by a Fragment Coupling Approach ACS Central Science; Vol. 7; No. 8; https://doi.org/10.1021/acscentsci.1c00540

• Holman, K. R.; Stanko, A. M. et al. (2021) Palladium-catalyzed cascade cyclizations involving C–C and C–X bond formation: strategic applications in natural product synthesis Chemical Society Reviews; Vol. 50; No. 14; https://doi.org/10.1039/d0cs01385d

• Maser, Michael R.; Reisman, Sarah E. (2021) 3D Computer Vision Models Predict DFT-Level HOMO-LUMO Gap Energies from Force-Field-Optimized Geometries https://doi.org/10.33774/chemrxiv-2021-11r61

• Gao, Yang; Hill, David E. et al. (2021) Electrochemical Nozaki–Hiyama–Kishi Coupling: Scope, Applications, and Mechanism Journal of the American Chemical Society; Vol. 143; No. 25; https://doi.org/10.1021/jacs.1c03007

• Brandstätter, Marco; Turro, Raymond F. et al. (2021) Nickel-Catalyzed Reductive Alkylation of Heteroaryl Imines https://doi.org/10.33774/chemrxiv-2021-mdjf6

• DeLano, Travis J.; Dibrell, Sara E. et al. (2021) Nickel-catalyzed asymmetric reductive cross-coupling of α-chloroesters with (hetero)aryl iodides Chemical Science; Vol. 12; No. 22; https://doi.org/10.1039/d1sc00822f

• Reisman, Sarah E.; Maimone, Thomas J. (2021) Total Synthesis of Complex Natural Products: More Than a Race for Molecular Summits Accounts of Chemical Research; Vol. 54; No. 8; https://doi.org/10.1021/acs.accounts.1c00184

• Nakayama, Yasuaki; Maser, Michael R. et al. (2021) Total Synthesis of Ritterazine B Journal of the American Chemical Society; Vol. 143; No. 11; https://resolver.caltech.edu/CaltechAUTHORS:20210202-123615131

• Dibrell, Sara E.; Tao, Yujia et al. (2021) Synthesis of Complex Diterpenes: Strategies Guided by Oxidation Pattern Analysis Accounts of Chemical Research; Vol. 54; No. 6; https://doi.org/10.1021/acs.accounts.0c00858

• Maser, Michael R.; Cui, Alexander Y. et al. (2021) Multilabel Classification Models for the Prediction of Cross-Coupling Reaction Conditions Journal of Chemical Information and Modeling; Vol. 61; No. 1; https://resolver.caltech.edu/CaltechAUTHORS:20201015-152733539

• Cowper, Nicholas G. W.; Hesse, Matthew J. et al. (2020) A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core Chemical Science; Vol. 11; No. 43; https://doi.org/10.1039/d0sc04802j

• Blom, Annet E. M.; Su, Justin Y. et al. (2020) Synthesis and Biological Evaluation of Pyrroloindolines as Positive Allosteric Modulators of the α1β2γ2 GABA_A Receptor ACS Medicinal Chemistry Letters; Vol. 11; No. 11; https://doi.org/10.1021/acsmedchemlett.0c00340

• Fastuca, Nicholas J.; Wong, Alice R. et al. (2020) Asymmetric Michael Addition of Dimethyl Malonate to 2 Cyclopenten-1-one Catalyzed by a Heterobimetallic Complex Organic Syntheses; Vol. 97; https://doi.org/10.15227/orgsyn.097.0327

• Reisman, Sarah E.; Sarpong, Richmond et al. (2020) Organic Chemistry: A Call to Action for Diversity and Inclusion ACS Central Science; Vol. 6; No. 8; https://doi.org/10.1021/acscentsci.0c01027

• Reisman, Sarah E.; Sarpong, Richmond et al. (2020) Organic Chemistry: A Call to Action for Diversity and Inclusion Organometallics; Vol. 39; No. 16; https://doi.org/10.1021/acs.organomet.0c00519

• Reisman, Sarah E.; Sarpong, Richmond et al. (2020) Organic Chemistry: A Call to Action for Diversity and Inclusion Journal of Organic Chemistry; Vol. 85; No. 16; https://doi.org/10.1021/acs.joc.0c01607

• Reisman, Sarah E.; Sarpong, Richmond et al. (2020) Organic Chemistry: A Call to Action for Diversity and Inclusion Organic Letters; Vol. 22; No. 16; https://doi.org/10.1021/acs.orglett.0c02559

• Hofstra, Julie L.; DeLano, Travis J. et al. (2020) 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) Organic Syntheses; Vol. 97; https://doi.org/10.15227/orgsyn.097.0172

• Poremba, Kelsey E.; Dibrell, Sara E. et al. (2020) Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions ACS Catalysis; Vol. 10; No. 15; https://doi.org/10.1021/acscatal.0c01842

• Ryou, Serim; Maser, Michael R. et al. (2020) Graph Neural Networks for the Prediction of Substrate-Specific Organic Reaction Conditions arXiv; https://resolver.caltech.edu/CaltechAUTHORS:20201110-154207213

• Wittmann, Bruce J.; Knight, Anders M. et al. (2020) Diversity-Oriented Enzymatic Synthesis of Cyclopropane Building Blocks ACS Catalysis; Vol. 10; No. 13; https://doi.org/10.1021/acscatal.0c01888

• Dibrell, Sara E.; Maser, Michael R. et al. (2020) SeO₂-Mediated Oxidative Transposition of Pauson–Khand Products Journal of the American Chemical Society; Vol. 142; No. 14; https://doi.org/10.1021/jacs.9b13818

• Reisman, Sarah E. (2020) Necessity is the mother of invention: Natural products and the chemistry they inspire In: 259th ACS National Meeting & Exposition, 22-26 March 2020, Philadelphia, PA https://resolver.caltech.edu/CaltechAUTHORS:20200219-133123539

• Reisman, Sarah E. (2020) Total synthesis of natural product antibiotics In: 259th ACS National Meeting & Exposition, 22-26 March 2020, Philadelphia, PA https://resolver.caltech.edu/CaltechAUTHORS:20200219-113059736

• Hofstra, Julie L.; Poremba, Kelsey E. et al. (2019) Nickel-Catalyzed Conversion of Enol Triflates into Alkenyl Halides Angewandte Chemie International Edition; Vol. 58; No. 42; https://doi.org/10.1002/anie.201906815

• Han, Arthur; Tao, Yujia et al. (2019) A 16-step synthesis of the isoryanodane diterpene (+)-perseanol Nature; Vol. 573; No. 7775; https://resolver.caltech.edu/CaltechAUTHORS:20190610-080930538

• DeLano, Travis J.; Reisman, Sarah E. (2019) Enantioselective Electroreductive Coupling of Alkenyl and Benzyl Halides via Nickel Catalysis ACS Catalysis; Vol. 9; No. 8; https://doi.org/10.1021/acscatal.9b01785

• Reisman, Sarah E. (2019) Building bridges: Strategies for the synthesis of polycyclic natural products In: 258th ACS National Meeting & Exposition, 25-29 August 2019, San Diego, CA https://resolver.caltech.edu/CaltechAUTHORS:20190812-092833141

• Reisman, Sarah E. (2019) Development of Ni-catalyzed enantioselective reductive cross-coupling reactions In: 258th ACS National Meeting & Exposition, 25-29 August 2019, San Diego, CA https://resolver.caltech.edu/CaltechAUTHORS:20190812-131105027

• Reisman, Sarah E. (2019) Necessity is the mother of invention: Natural products and the chemistry they inspire In: 258th ACS National Meeting & Exposition, 25-29 August 2019, San Diego, CA https://resolver.caltech.edu/CaltechAUTHORS:20190812-100104064

• Mendoza, Skyler Dakota; Reisman, Sarah E. (2019) Progress toward the total synthesis of falcatin A In: 257th ACS National Meeting & Exposition, 31 March - 4 April 2019, Orlando, FL https://resolver.caltech.edu/CaltechAUTHORS:20190325-091013157

• Beck, Jordan C.; Lacker, Caitlin R. et al. (2019) A modular approach to prepare enantioenriched cyclobutanes: synthesis of (+)-rumphellaone A Chemical Science; Vol. 10; No. 8; https://doi.org/10.1039/c8sc05444d

• Carreira, Erick M.; Brimble, Margaret et al. (2019) Organic Letters 2.0: A New Beginning Organic Letters; Vol. 21; No. 1; https://doi.org/10.1021/acs.orglett.8b03964

• Su, Justin Y.; Grünenfelder, Denise C. et al. (2018) Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides Organic Letters; Vol. 20; No. 16; https://doi.org/10.1021/acs.orglett.8b02045

• Reisman, Sarah (2018) Synthetic studies toward ryanodol, ryanodine, and related insecticidal natural products In: 256th American Chemical Society National Meeting & Exposition, 19-23 August 2018, Boston, MA https://resolver.caltech.edu/CaltechAUTHORS:20181101-132923115

• Xu, Chen; Han, Arthur et al. (2018) An Oxidative Dearomatization Approach To Prepare the Pentacyclic Core of Ryanodol Organic Letters; Vol. 20; No. 13; https://doi.org/10.1021/acs.orglett.8b01387

• Chapman, Lauren M.; Beck, Jordan C. et al. (2018) Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B Journal of Organic Chemistry; Vol. 83; No. 11; https://doi.org/10.1021/acs.joc.8b00728

• Reisman, Sarah (2018) Necessity is the mother of invention: Natural products and the chemistry they inspire In: 255th American Chemical Society National Meeting & Exposition, March 18-22, 2018, New Orleans, LA https://resolver.caltech.edu/CaltechAUTHORS:20180413-084731744

• Farney, Elliot P.; Feng, Sean S. et al. (2018) Total Synthesis of (+)-Pleuromutilin Journal of the American Chemical Society; Vol. 140; No. 4; https://doi.org/10.1021/jacs.7b13260

• Hofstra, Julie L.; Cherney, Alan H. et al. (2018) Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling Journal of the American Chemical Society; Vol. 140; No. 1; https://doi.org/10.1021/jacs.7b11707

• Reisman, Sarah (2017) Building bridges: Strategies and tactics for the synthesis of polycyclic natural products In: 254th American Chemical Society National Meeting & Exposition, August 20-24, 2017, Washington, DC https://resolver.caltech.edu/CaltechAUTHORS:20170913-083334553

• Reisman, Sarah E. (2017) Enantioselective Ni-catalyzed cross-electrophile coupling In: 254th American Chemical Society National Meeting & Exposition, August 20-24, 2017, Washington, DC https://resolver.caltech.edu/CaltechAUTHORS:20170911-152059005

• Xu, Chen; Han, Arthur et al. (2017) Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine ACS Central Science; Vol. 3; No. 4; https://doi.org/10.1021/acscentsci.6b00361

• Poremba, Kelsey E.; Kadunce, Nathaniel T. et al. (2017) Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes Journal of the American Chemical Society; Vol. 139; No. 16; https://doi.org/10.1021/jacs.7b01705

• Suzuki, Naoyuki; Hofstra, Julie L. et al. (2017) Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides Organic Letters; Vol. 19; No. 8; https://doi.org/10.1021/acs.orglett.7b00793

• Wang, Haoxuan; Regan, Clinton J. et al. (2017) Enantioselective Synthesis of (−)-Acetylapoaranotin Organic Letters; Vol. 19; No. 7; https://doi.org/10.1021/acs.orglett.7b00418

• Beck, Jordan C.; Reisman, Sarah E. (2017) Development of a unified strategy for the syntheis of enmein-type ent-kauranoids In: 253rd American Chemical Society National Meeting & Exposition, April 2-6, 2017, San Francisco, CA https://resolver.caltech.edu/CaltechAUTHORS:20170502-080053912

• Reisman, Sarah E. (2017) Necessity is the mother of invention: Natural products and the chemistry they inspire In: 253rd American Chemical Society National Meeting & Exposition, April 2-6, 2017, San Francisco, CA https://resolver.caltech.edu/CaltechAUTHORS:20170503-143336033

• Hofstra, Julie; Suzuki, Naoyuki et al. (2017) Nickel-catalyzed asymmetric reductive cross-couplings with vinyl bromide electrophiles In: 253rd American Chemical Society National Meeting & Exposition, April 2-6, 2017, San Francisco, CA https://resolver.caltech.edu/CaltechAUTHORS:20170503-104847932

• Chuang, Kangway V.; Kieffer, Madeleine E. et al. (2016) A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans Organic Letters; Vol. 18; No. 18; https://doi.org/10.1021/acs.orglett.6b02477

• Reisman, Sarah E.; Kieffer, Madeleine E. et al. (2016) Asymmetric Dearomatization via Cycloaddition Reaction In: Asymmetric Dearomatization Reactions; https://doi.org/10.1002/9783527698479.ch7

• Chuang, Kangway V.; Xu, Chen et al. (2016) A 15-step synthesis of (+)-ryanodol Science; Vol. 353; No. 6302; https://doi.org/10.1126/science.aag1028

• Chapman, Lauren M.; Beck, Jordan C. et al. (2016) Enantioselective Total Synthesis of (+)-Psiguadial B Journal of the American Chemical Society; Vol. 138; No. 31; https://doi.org/10.1021/jacs.6b07229

• Reisman, Sarah (2016) Enantioselective Ni-catalyzed reductive cross-coupling reactions In: 252nd American Chemical Society National Meeting & Exposition, 21-25 August 2016, Philadelphia, PA https://resolver.caltech.edu/CaltechAUTHORS:20160913-083628711

• Reisman, Sarah (2016) Necessity is the mother of invention: Natural products and the chemistry they inspire In: 252nd American Chemical Society National Meeting & Exposition, 21-25 August 2016, Philadelphia, PA https://resolver.caltech.edu/CaltechAUTHORS:20160913-122803637

• Daniels, Blake E.; Ni, Jane et al. (2016) Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction Angewandte Chemie International Edition; Vol. 55; No. 10; https://doi.org/10.1002/anie.201510972

• Cherney, Alan H.; Kadunce, Nathaniel T. et al. (2015) Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C–C Bonds Chemical Reviews; Vol. 115; No. 17; https://doi.org/10.1021/acs.chemrev.5b00162

• Kadunce, Nathaniel T.; Reisman, Sarah E. (2015) Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles Journal of the American Chemical Society; Vol. 137; No. 33; https://doi.org/10.1021/jacs.5b06466

• Jang, Kyoung-Soon; Nani, Roger R. et al. (2015) A cationic cysteine-hydrazide as an enrichment tool for the mass spectrometric characterization of bacterial free oligosaccharides Analytical and Bioanalytical Chemistry; Vol. 407; No. 20; https://doi.org/10.1007/s00216-015-8798-8

• Chapman, Lauren M.; Reisman, Sarah E. (2015) Progress toward the total synthesis of psiguadial B In: 250th American Chemical Society National Meeting & Exposition, August 16-20, 2015, Boston, MA https://resolver.caltech.edu/CaltechAUTHORS:20150916-130810447

• Reisman, Sarah E. (2015) From alkaloids to terpenoids: New strategies and tactics for the synthesis of polycyclic natural products Abstracts of Papers of the American Chemical Society; Vol. 249; In: 249th American Chemical Society National Meeting & Exposition, March 22-26, 2015, Denver, CO https://resolver.caltech.edu/CaltechAUTHORS:20150408-081804123

• Cherney, Alan H.; Reisman, Sarah E. (2014) Nickel-Catalyzed Asymmetric Reductive Cross-Coupling Between Vinyl and Benzyl Electrophiles Journal of the American Chemical Society; Vol. 136; No. 41; https://doi.org/10.1021/ja508067c

• Reisman, Sarah E. (2014) Natural product synthesis: A platform for discovery in chemistry and biology In: 248th American Chemical Society National Meeting & Exposition, August 10-14, 2014, San Francisco, CA https://resolver.caltech.edu/CaltechAUTHORS:20140811-145022145

• Yeoman, John T. S.; Cha, Jacob Y. et al. (2014) A unified strategy for the synthesis of (−)-maoecrystal Z, (−)-trichorabdal A, and (−)-longikaurin E Tetrahedron; Vol. 70; No. 27-28; https://doi.org/10.1016/j.tet.2014.03.071

• Wang, Haoxuan; Reisman, Sarah E. (2014) Enantioselective Total Synthesis of (-)-Lansai B and (+)-Nocardioazines A and B Angewandte Chemie International Edition; Vol. 53; No. 24; https://doi.org/10.1002/anie.201402571

• Cherney, Alan H.; Reisman, Sarah E. (2014) Pd-catalyzed Fukuyama cross-coupling of secondary organozinc reagents for the direct synthesis of unsymmetrical ketones Tetrahedron; Vol. 70; No. 20; https://doi.org/10.1016/j.tet.2013.11.104

• Repka, Lindsay M.; Reisman, Sarah E. (2013) Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters Journal of Organic Chemistry; Vol. 78; No. 24; https://doi.org/10.1021/jo4017953

• Hsiao, Elaine Y.; McBride, Sara W. et al. (2013) Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders Cell; Vol. 155; No. 7; https://doi.org/10.1016/j.cell.2013.11.024

• Reisman, Sarah E. (2013) Natural Product Synthesis: A Platform for Chemical Discovery In: 44th American Chemical Society Western Regional Meeting, October 3-6, 2013, Santa Clara, CA https://resolver.caltech.edu/CaltechAUTHORS:20131112-080054809

• Reisman, Sarah E. (2013) Award Address (Arthur C. Cope Scholar Awards (CSY) sponsored by Arthur C. Cope Fund). Natural product synthesis: A platform for chemical discovery In: 246th ACS National Meeting & Exposition, Sept. 8-12, 2013, Indianapolis, IN https://resolver.caltech.edu/CaltechAUTHORS:20131011-110722162

• Reisman, Sarah E. (2013) Discoveries and diversions in natural product synthesis In: 246th ACS National Meeting & Exposition, Sept. 8-12, 2013, Indianapolis, IN https://resolver.caltech.edu/CaltechAUTHORS:20140213-145722485

• Yeoman, John T. S.; Mak, Victor W. et al. (2013) A Unified Strategy to ent-Kauranoid Natural Products: Total Syntheses of (−)-Trichorabdal A and (−)-Longikaurin E Journal of the American Chemical Society; Vol. 135; No. 32; https://doi.org/10.1021/ja406599a

• Wang, Jane Ni Haoxuan; Reisman, Sarah E. (2013) Direct, enantioselective synthesis of pyrroloindolines and indolines from simple indole derivatives Tetrahedron; Vol. 69; No. 27-28; https://doi.org/10.1016/j.tet.2013.04.003

• Reisman, Sarah E. (2013) Natural Product Synthesis: A Platform for Chemical Discovery In: 68th Northwest Regional Meeting of the American Chemical Society, July 21-24, 2013, Corvallis, OR https://resolver.caltech.edu/CaltechAUTHORS:20131009-085028526

• Cherney, Alan H.; Kadunce, Nathaniel T. et al. (2013) Catalytic Asymmetric Reductive Acyl Cross-Coupling: Synthesis of Enantioenriched Acyclic α,α-Disubstituted Ketones Journal of the American Chemical Society; Vol. 135; No. 20; https://doi.org/10.1021/ja402922w

• Nani, Roger R.; Reisman, Sarah E. (2013) α-Diazo-β-ketonitriles: Uniquely Reactive Substrates for Arene and Alkene Cyclopropanation Journal of the American Chemical Society; Vol. 135; No. 19; https://doi.org/10.1021/ja401610p

• Kieffer, Madeleine E.; Chuang, Kangway V. et al. (2013) Copper-Catalyzed Diastereoselective Arylation of Tryptophan Derivatives: Total Synthesis of (+)-Naseseazines A and B Journal of the American Chemical Society; Vol. 135; No. 15; https://doi.org/10.1021/ja4023557

• Codelli, Julian A.; Reisman, Sarah E. (2013) Pactamycin Made Easy Science; Vol. 340; No. 6129; https://doi.org/10.1126/science.1236882

• Reisman, Sarah E. (2013) New methods and strategies for the enantioselective synthesis of polycyclic natural products In: 245th ACS National Meeting & Exposition, Abstracts of Papers, April 7-11, 2013, New Orleans, LA https://resolver.caltech.edu/CaltechAUTHORS:20130410-101421544

• Lim, Andrew D.; Codelli, Julian A. et al. (2012) Catalytic asymmetric synthesis of highly substituted pyrrolizidines Chemical Science; Vol. 4; No. 2; https://doi.org/10.1039/c2sc21617e

• Kieffer, Madeleine E.; Chuang, Kangway V. et al. (2012) A copper-catalyzed arylation of tryptamines for the direct synthesis of aryl pyrroloindolines Chemical Science; Vol. 3; No. 11; https://doi.org/10.1039/c2sc20914d

• Yeoman, John T. S.; Reisman, Sarah E. (2012) Single molecules put a ring on it Nature; Vol. 490; No. 7419; https://doi.org/10.1038/490179a

• Navarro, Raul; Reisman, Sarah E. (2012) Rapid Construction of the Aza-Propellane Core of Acutumine via a Photochemical [2 + 2] Cycloaddition Reaction Organic Letters; Vol. 14; No. 17; https://doi.org/10.1021/ol3017963

• Kieffer, Madeleine E.; Repka, Lindsay M. et al. (2012) Enantioselective Synthesis of Tryptophan Derivatives by a Tandem Friedel–Crafts Conjugate Addition/Asymmetric Protonation Reaction Journal of the American Chemical Society; Vol. 134; No. 11; https://doi.org/10.1021/ja209390d

• Codelli, Julian A.; Puchlopek, Angela L. A. et al. (2012) Enantioselective Total Synthesis of (—)-Acetylaranotin, a Dihydrooxepine Epidithiodiketopiperazine Journal of the American Chemical Society; Vol. 134; No. 4; https://doi.org/10.1021/ja209354e

• Reisman, Sarah E.; Nani, Roger R. et al. (2011) Buchner and Beyond: Arene Cyclopropanation as Applied to Natural Product Total Synthesis Synlett; Vol. 2011; No. 17; https://doi.org/10.1055/s-0031-1289520

• Cha, Jacob Y.; Yeoman, John T. S. et al. (2011) A Concise Total Synthesis of (--)-Maoecrystal Z Journal of the American Chemical Society; Vol. 133; No. 38; https://doi.org/10.1021/ja2073356

• Chuang, Kangway V.; Navarro, Raul et al. (2011) Short, Enantioselective Total Syntheses of (—)-8-Demethoxyrunanine and (—)-Cepharatines A, C, and D Angewandte Chemie International Edition; Vol. 50; No. 40; https://doi.org/10.1002/anie.201104487

• Reisman, Sarah E. (2011) Medicinal chemistry: New lead for pain treatment Nature; Vol. 473; No. 7348; https://doi.org/10.1038/473458a

• Chuang, Kangway V.; Navarro, Raul et al. (2011) Benzoquinone-derived sulfinyl imines as versatile intermediates for alkaloid synthesis: Total synthesis of (–)-3-demethoxyerythratidinone Chemical Science; Vol. 2; No. 6; https://doi.org/10.1039/C1SC00095K

• Levin, Sergiy; Nani, Roger R. et al. (2011) Enantioselective Total Synthesis of (+)-Salvileucalin B Journal of the American Chemical Society; Vol. 133; No. 4; https://doi.org/10.1021/ja110192b

• Repka, Lindsay M.; Ni, Jane et al. (2010) Enantioselective Synthesis of Pyrroloindolines by a Formal [3 + 2] Cycloaddition Reaction Journal of the American Chemical Society; Vol. 132; No. 41; https://doi.org/10.1021/ja107328g

• Freeman, David B.; Holubec, Alexandra A. et al. (2010) Welwitindolinone C synthetic studies. Construction of the welwitindolinone carbon skeleton via a transannular nitrone cycloaddition Tetrahedron; Vol. 66; No. 33; https://doi.org/10.1016/j.tet.2010.04.131

• Levin, Sergiy; Nani, Roger R. et al. (2010) Rapid Assembly of the Salvileucalin B Norcaradiene Core Organic Letters; Vol. 12; No. 4; https://doi.org/10.1021/ol902848k

• Reisman, Sarah E.; Doyle, Abigail G. et al. (2008) Enantioselective Thiourea-Catalyzed Additions to Oxocarbenium Ions Journal of the American Chemical Society; Vol. 130; No. 23; https://doi.org/10.1021/ja801514m

• Reisman, Sarah E.; Ready, Joseph M. et al. (2008) Evolution of a Synthetic Strategy: Total Synthesis of (±)-Welwitindolinone A Isonitrile Journal of the American Chemical Society; Vol. 130; No. 6; https://doi.org/10.1021/ja076663z

• Reisman, Sarah E.; Ready, Joseph M. et al. (2006) Total Synthesis of (±)-Welwitindolinone A Isonitrile Journal of the American Chemical Society; Vol. 128; No. 5; https://doi.org/10.1021/ja057640s

• Ready, Joseph M.; Reisman, Sarah E. et al. (2004) A Mild and Efficient Synthesis of Oxindoles: Progress Towards the Synthesis of Welwitindolinone A Isonitrile Angewandte Chemie International Edition; Vol. 43; No. 10; https://doi.org/10.1002/anie.200353282

• Ovaska, Timo V.; Reisman, Sarah E. et al. (2001) Facile Entry to the Tetracyclic 5-7-6-3 Tigliane Ring System Organic Letters; Vol. 3; No. 1; https://doi.org/10.1021/ol006823a