90. Ni-Catalyzed Asymmetric Reductive Arylation of α-Substituted Imides. Chen L. M.; Shin C.; DeLano T.; Carretero-Cerdán A.; Gheibi G.; Reisman S. E. J. Am. Chem. Soc., 2024 DOI: https://doi.org/10.1021/jacs.4c09327​
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89. Ni-Catalyzed Enantioselective Desymmetrization: Development of Divergent Acyl and Decarbonylative Cross-Coupling Reactions. Hernández-Mejías A.; Shimozono A.; Hazra A.; Richter S.; Tong Z.; Langille N.; Quasdorf K.; Parsons A.; Sigman M.; Reisman S. E. ChemRxiv, 2024 DOI: https://chemrxiv.org/engage/chemrxiv/article-details/66edb5b951558a15ef98542f​
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88. Reductive Samarium (electro)catalysis Enabled by SmIII-alkoxide protonolysis. Boyd E. A.†; Shin C.†; Charboneau D. J.; Peters J. C.; Reisman S. E. Science, 2024, 385, 847–853 DOI: https://doi.org/10.1126/science.adp5777​
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87. Enantioselective C(sp2)–C(sp3) Bond Construction by Ni Catalysis Chen L. M.; Reisman S. E. Acc. Chem. Res., 2024 DOI: doi.org/10.1021/acs.accounts.3c00775​
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86. Electrocatalytic Asymmetric Nozaki–Hiyama–Kishi Decarboxylative Coupling: Scope, Applications, and Mechanism Gao Y.; Jiang B.; Friede N. C.; Hunter A. C.; Boucher D. G.; Minteer S. D.; Sigman M. S.; Reisman S. E.; Baran P. S. J. Am. Chem. Soc., 2024 DOI: doi.org/10.1021/jacs.3c13442​
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85. Ni-Catalyzed Asymmetric Reductive Arylation of ⍺-Substituted Imides. Chen L. M.; Shin C. K.; Delano T.; Reisman S. E. ChemRxiv, 2023 21 December 2023, Version 1 DOI: 10.26434/chemrxiv-2023-97hjq​
84. Dataset design for building models of chemical reactivity. Raghavan P.; Haas B. C.; Ruos M. E.; Schleinitz J.; Doyle A. G.; Reisman S. E.; Sigman M. S.; Coley C. W. ACS Cent. Sci. 2023 9, 12, 2196–2204 DOI: doi.org/10.1021/acscentsci.3c01163​
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83. A Pyridine Dearomatization Approach for the Gram Scale Synthesis of ()-Sparteine. Lam, P. H.; Kerkovius, J. K.; Reisman, S. E. Org. Lett. 2023. DOI: doi.org/10.1021/acs.orglett.3c03242​
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82. Isolation, biosynthesis, and chemical syntheses of the hasubanan and acutumine alkaloids: A historical perspective. Grünenfelder, D. C.; Reisman, S. E.; Navarro, R. Tetrahedron. 2023, 149, 133709. DOI: doi.org/10.1016/j.tet.2023.133709​
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81. Development of a Nickel-Catalyzed N–N Coupling for the Synthesis of Hydrazides. Barbor, J. P.; Nair, V. N.; Sharp, K. R.; Lohrey, T. D.; Dibrell, S. E.; Shah, T. K.; Walsh, M. J.; Reisman, S. E.; Stoltz, B. M. J. Am. Chem. Soc. 2023, 145, 28, 15071. DOI: doi.org/10.1021/jacs.3c04834​
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80. Mechanistic Investigation of Ni-Catalyzed Reductive Cross-Coupling of Alkenyl and Benzyl Electrophiles. Turro, R. F.; Wahlman, J. L. H.; Tong, Z. J.; Chen, X.; Yang, M.; Chen, E. P.; Hong, X.; Hadt, R. G.; Houk, K. N.; Yang, Y.; Reisman, S. E. J. Am. Chem. Soc. 2023, 145, 27, 14705. DOI: doi.org/10.1021/jacs.3c02649​
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79. Electronic Structures of Nickel(II)-Bis(indanyloxazoline)-dihalide Catalysts: Understanding Ligand Field Contributions that Promote C(sp2)–C(sp3) Cross-Coupling. McNicholas, B. J.; Tong, J.; Bím, D.; Turro, R. F.; Kazmierczak, N. P.; Chalupský, J.; Reisman, S. E.; Hadt, R. G. Inorg. Chem. 2023. DOI: doi.org/10.1021/acs.inorgchem.3c02048​
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78. Electrochemical Preparation of Sm(II) Reagent Facilitated by Weakly Coordinating Anions. Ware, S. D.; Zhang, W.; Charboneau, D. J.; Klein, C. K.; Reisman, S. E.; See, K. A. Chem. Eur. J. 2023, 29, e202301045. DOI: doi.org/10.1002/chem.202301045​
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77. A convergent fragment coupling strategy to access quaternary stereogenic centers Kerkovius, J. K.; Wong, A. R.; Mak, V. W.; Reisman, S. E. Chem. Sci. 2023 DOI: doi.org/10.1039/D2SC07023E​
76. Enantioselective Synthesis of N-Benzylic Heterocycles by Ni/Photoredox Dual Catalysis Lacker, C. R.; Delano, T. J.; Chen, E. P.; Kong, J.; Belyk, K. M.; Piou, T.; Reisman, S. E. J. Am. Chem. Soc. 2022,144, 20190 DOI: doi.org/10.1021/jacs.2c07917​
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75. A Pyridine Dearomatization Approach to the Matrine–Type Lupin Alkaloids. Kerkovius, J. K.; Stegner, A.; Turlik, A.; Lam, P.H.; Houk, K.N.; Reisman, S. E. J. Am. Chem. Soc. 2022, 144, 15938 DOI: doi.org/10.1021/jacs.2c06584​
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74. Expanding the Chiral Monoterpene Pool: Enantioselective Diels–Alder Reactions of α–Acyloxy Enones. Mendoza, S. D.; Rombola, M.; Tao, Y.; Zuend, S. J.; Götz, R.; McLaughlin, M. J.; Reisman, S. E. Org. Lett. 2022, 24, 3802. DOI: doi.org/10.1021/acs.orglett.2c01343​
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73. Synthesis of Noraugustamine and Development of an Oxidative Heck/Aza-Wacker Cascade Cyclization. Holman, K. R.; Stanko, A.M.; Richter, M.J.R.; Feng, S. S.; Gessesse, M. N.; Reisman, S. E. Org. Lett. 2022, 24, 3019. DOI: doi.org/10.1021/acs.orglett.2c00948​
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72. Enantioselective Synthesis of (–)-C10-Hydroxyacutuminine. Grünenfelder, D. C.; Navarro, R.; Wang, H.; Fastuca, N. J.; Butler, J. R.; Reisman, S. E. Angew. Chem. Int. Ed. 2022, 62, e202117480. DOI: 10.1002/anie.202117480​
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71. Plugging the Leak: Empowering Women in Organic Chemistry.  Dibrell, S. E.; Holman, K. R.; Reisman, S. E.  Angew. Chem. Int. Ed. 2022, 61, e202111765. DOI: 10.1002/anie.202111765
70. Cobalt-Electrocatalytic Hydrogen Atom Transfer for Functionalization of Unsaturated C–C Bonds.  Gnaim, S.; Bauer, A.; Zhang, H.-J.; Chen, L.; Gannet, C.; Malapit, C. A.; Hill, D. E.; Vogt, D.; Tang, T.; Daley, R.; Hao, W.; Quertenmont, M.; Beck, W. D.; Kandahari, E.; Vantourout, J. C.; Echeverria, P.-G.; Abruna, H.; Blackmond, D. G.; Minteer, S.; Reisman, S. E.; Sigman, M. S.; Baran, P. S. Nature 2022, 605, 687
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69. 3D Computer Vision Models Predict DFT-Level HOMO-LUMO Gap Energies from Force-Field-Optimized Geometries. Maser, M. R.; Reisman, S. E. ChemRxiv
68. Nickel-Catalyzed Reductive Alkylation of Heteroaryl Imines. Turro, R. F.; Brandstätter, M.; Reisman, S. E. Angew. Chem. Int. Ed. 2022 e202207597 DOI:10.1002/anie.202207597
67. Electrochemical Nozaki–Hiyama–Kishi Coupling: Scope, Applications, and Mechanism. Gao, Y.; Hill, D. E.; Hao, W.; McNicholas, B. J.; Vantourout, J. C.; Hadt, R. G.; Reisman, S. E.; Blackmond, D. G.; Baran, P. S. J. Am. Chem. Soc. 2021, 143, 9478. DOI: 10.1021/jacs.1c03007
66. Total Syntheses of the C19 Diterpenoid Alkaloids (–)-Talatisamine, (–)-Liljestrandisine, and (–)-Liljestrandinine by a Fragment Coupling Approach. Wong, A. R.; Fastuca, N. J.; Mak, V. W.; Kerkovius, J. K.; Stevenson, S. M.; Reisman, S. E. ACS Cent. Sci. 2021, 7, 1311. DOI: 10.1021/acscentsci.1c00540.
65. Palladium-Catalyzed Cascade Cyclizations Involving C–C and C–X Bond Formation: Strategic Applications in Natural Product Synthesis. Holman, K. R.; Stanko, A. M.; Reisman, S. E. Chem. Soc. Rev. 2021, 50, 7891. DOI: ​10.1039/D0CS01385D
64. Total Synthesis of Complex Natural Products: More Than a Race for Molecular Summits. Reisman, S. E.; Maimone, T. J. Acc. Chem. Res. 2021, 54, 1815. DOI: 10.1021/acs.accounts.1c00184
63. Synthesis of Complex Diterpenes: Strategies Guided by Oxidation Pattern Analysis. Dibrell, S. E.; Tao, Y.; Reisman, S. E. Acc. Chem. Res. 2021, 54, 1360. DOI: 10.1021/acs.accounts.0c00858
62. Total Synthesis of Ritterazine B. Nakayama, N.; Maser, M. R.; Okita, T.; Dubrovskiy, A. V.; Campbell, T. L.; Reisman, S. E. J. Am. Chem. Soc. 2021, 143, 4187. DOI: 10.1021/jacs.1c01372
61. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling of a-Chloroesters with (Hetero)Aryl Iodides. DeLano, T. J.; Dibrell, S. E.; Lacker, C. R.; Pancoast, A. R.; Poremba, K. E.; Cleary, L. B.; Sigman, M. S.; Reisman, S. E. Chem. Sci. 2021, 12, 7758. DOI: 10.1039/D1SC00822F
60. Multi-Label Classification Models for the Prediction of Cross-Coupling Reaction Conditions. Maser, M. R.; Cui, A. Y.; Ryou, S.; DeLano, T. J.; Yue, Y.; Reisman, S. E. J. Chem. Inf. Model. 2021, 61, 156. DOI: 10.1021/acs.jcim.0c01234
59. Asymmetric Michael Addition of Dimethyl Malonate to 2-Cyclopenten-1-one Catalyzed by a Heterobimetallic Complex.​ Fastuca, N. J.; Wong, A. R.; Mak, V. W.; Reisman, S. E. Org. Synth. 2020, 97, 327. DOI: 10.15227/orgsyn.097.0327
58. A Copper-Catalyzed Asymmetric Oxime Propargylation Enables the Synthesis of the Gliovirin Tetrahydro-1,2-oxazine Core. Cowper, N. G. W.; Hesse, M. J.; Chan, K. M.; Reisman, S. E. Chem. Sci. 2020, 11, 11897. DOI: 10.1039/D0SC04802J
57. Synthesis and Biological Evaluation of Pyrroloindolines as Positive Allosteric Modulators of the α1β2γ2 GABAA Receptor. Blom, A. E. M.; Su, J. Y.; Repka, L. M.; Reisman, S. E.; Dougherty, D. A. ACS Med. Chem. Lett. 2020, 11, 2204. DOI: 10.1021/acsmedchemlett.0c00340
56. 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). Hofstra, J. L.; DeLano, T. J.; Reisman, S. E. Org. Synth. 2020, 97, 172. DOI: 10.15227/orgsyn.097.0172
55. Organic Chemistry: A Call to Action for Diversity and Inclusion. Reisman, S. E.; Sarpong, R.; Sigman, M. S.; Yoon, T. P. J. Org. Chem. 2020, 85, 10287. DOI: 10.1021/acs.joc.0c01607
54. Graph Neural Networks for the Prediction of Substrate-Specific Organic Reaction Conditions. Ryou, S.; Maser, M. R.; Cui, A. Y.; DeLano, T. J.; Yue, Y.; Reisman, S. E. arXiv: 2007.04275 [cs.LG]. Appeared in the ICML 2020 workshop on Graph Representation Learning and Beyond (GRLB). Slides from the presentation can be found here. 
53. Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions. Poremba, K. E.; Dibrell, S. E.; Reisman, S. E. ACS Catal. 2020, 10, 8237. DOI: 10.1021/acscatal.0c01842
52. Diversity-Oriented Enzymatic Synthesis of Cyclopropane Building Blocks. Wittmann, B. J.; Knight, A. M.; Hofstra, J. L.; Reisman, S. E.; Kan, J.; Arnold, F. H. ACS Catal. 2020, 10, 7112. DOI: 10.1021/acscatal.0c01888
51. SeO2-mediated Oxidative Transposition of Pauson–Khand Products. Dibrell, S. E.; Maser, M.; Reisman, S. E. J. Am. Chem. Soc. 2020, 142, 6483. DOI: 10.1021/jacs.9b13818
50. A 16-step synthesis of the isoryanodane diterpene (+)–perseanol. Han, A.; Tao, Y.; Reisman, S. E. Nature 2019, 573, 563. DOI: 10.1038/s41586-019-1580-x. This synthesis was featured in C&EN, Chemistry World, The Cyclo Edition, and Org. Chem. Highlights.
49. Ni-Catalyzed Conversion of Enol Triflates to Alkenyl Halides. Hofstra, J. L.; Poremba, K. E.; Shimozono, A. M.; Reisman, S. E. Angew. Chem. Int. Ed. 2019, 58, 14901-14905. DOI: 10.1002/anie.201906815
48. Enantioselective Electroreductive Coupling of Alkenyl and Benzyl Halides via Nickel Catalysis. DeLano, T. J.; Reisman, S. E. ACS Catal. 2019, 9, 6751. DOI: 10.1021/acscatal.9b01785. This method was featured in OPR&D.
47. A Modular Approach to Prepare Enantioenriched Cyclobutanes: Synthesis of (+)-Rumphellaone A. Beck, J. C.; Lacker, C. R.; Chapman, L. M.; Reisman, S. E. Chem. Sci. 2019, 10, 2315. DOI: 10.1039/C8SC05444D. This method was featured in Chemistry World.
46. Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides. Su, J. Y.; Grünenfelder, D. C.; Takeuchi, K.; Reisman, S. E. Org. Lett. 2018, 20, 4912. DOI: 10.1021/acs.orglett.8b02045
45. An Oxidative Dearomatization Approach To Prepare the Pentacyclic Core of Ryanodol. Xu, C.; Han, A.; Reisman, S. E. Org. Lett. 2018, 20, 3793. DOI: 10.1021/acs.orglett.8b01387
44. Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B. Chapman, L. M.; Beck, J. C.; Lacker, C. R.; Reisman, S. E. J. Org. Chem. 2018, 83, 6066. DOI: 10.1021/acs.joc.8b00728
43. Total Synthesis of (+)-Pleuromutilin. Farney, E. P.; Feng, S. S.; Schäfers, F.; Reisman, S. E. J. Am. Chem. Soc. 2018, 140, 1267. DOI: 10.1021/jacs.7b13260. 
42. Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling. Hofstra, J. L.; Cherney, A. H.; Ordner, C. M.; Reisman, S. E. J. Am. Chem. Soc. 2018, 140, 139. DOI: 10.1021/jacs.7b11707
41. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes. Poremba, K. E.; Kadunce, N. T.; Suzuki, N.; Cherney, A. H.; Reisman, S. E. J. Am. Chem. Soc. 2017, 139, 5684. DOI: 10.1021/jacs.7b01705
40. Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides. Suzuki, N.; Hofstra, J. L.; Poremba, K. E.; Reisman, S. E. Org. Lett. 2017, 19, 2150. DOI: 10.1021/acs.orglett.7b00793
39. Enantioselective Synthesis of (–)-Acetylapoaranotin. Wang, H.; Regan, C. J.; Codelli, J. A.; Romanato, P.; Puchlopek-Dermenci, A. L. A.; Reisman, S. E.  Org. Lett. 2017, 19, 1698. DOI: 10.1021/acs.orglett.7b00418
38. Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine. Xu, C.; Han, A..; Virgil, S. C.; Reisman, S. E. ACS Cent. Sci. 2017, 3, 278. DOI: 10.1021/acscentsci.6b00361
37. A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans. Chuang, K. V.; Kieffer, M. E.; Reisman, S. E. Org. Lett. 2016, 18, 4750. DOI: 10.1021/acs.orglett.6b02477
36. A 15-step synthesis of (+)-ryanodol. Chuang, K. V.; Xu, C.; Reisman, S. E. Science. 2016, 353, 912. DOI: 10.1126/science.aag1028. This synthesis was featured in C&EN and Forbes. 
35. Enantioselective Total Synthesis of (+)-Psiguadial B. Chapman, L. M.; Beck, J. C.; Wu, L.; Reisman, S. E. J. Am. Chem. Soc. 2016, 138, 9803. DOI: 10.1021/jacs.6b07229. This synthesis was featured in an August C&E News article, Chem. Eng. News 2016, 94, 9, and Synfacts 2016, 12, 1003.
34. Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction. Daniels, B. E.; Ni, J.; Reisman, S. E. ​Angew. Chem. Int. Ed. 2016, 55, 3398. DOI: 10.1002/anie.201510972
33. Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents to Construct C–C Bonds. Cherney, A. H.; Kadunce, N. T.; Reisman, S. E. ​Chem. Rev. 2015, 115, 9587. DOI: 10.1021/acs.chemrev.5b00162
32. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling Between Heteroaryl Iodides and α-Chloronitriles. Kadunce, N. T.; Reisman, S. E.  J. Am. Chem. Soc. 2015, 137, 10480. DOI: ​10.1021/jacs.5b06466.
31. A Cationic Cysteine-Hydrazide as an Enrichment Tool for the Mass Spectrometric Characterization of Bacterial Free Oligosaccharides. Jang, K.-S.; Nani, R. R.; Kalli, A.; Levin, S.; Müller, A.; Hess, S.; Reisman, S. E.; Clemons, W. M. Jr. Anal. Bioanal. Chem. 2015, 407, 6181. DOI: ​10.1007/s00216-015-8798-8.
30. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling Between Vinyl and Benzyl Electrophiles. Cherney, A. H.; Reisman, S. E. J. Am. Chem. Soc. 2014, 136, 14365. DOI: ​10.1021/ja508067c.
29. Enantioselective Total Synthesis of (–)-Lansai B and (+)-Nocardioazines A and B. Wang, H.; Reisman, S. E. Angew. Chem. Int. Ed. 2014, 53, 6206. DOI: 10.1002/anie.201402571. This synthesis was featured in a September 2014 post on The Offset, which can be found here.
28. A Unified Strategy for the Synthesis of (–)-Maoecrystal Z, (–)-Trichorabdal A, and (–)-Longikaurin E. Yeoman, J. T. S.; Cha, J. Y.; Mak, V. M.; Reisman, S. E. Tetrahedron. 2014, 70, 4070. DOI: ​10.1016/j.tet.2014.03.071.
27. Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders. Hsiao, E. Y.; McBride, S. W.; Hsien, S.; Sharon, G.; Hyde, E. R.; McCue, T.; Codelli, J. A.; Chow, J.; Reisman, S. E.; Petrosino, J. F.; Patterson, P. H.; Mazmanian, S. K. Cell. 2013, 155, 1451. DOI: ​10.1016/j.cell.2013.11.024.
26. Pd-Catalyzed Fukuyama Cross-Coupling of Secondary Organozinc Reagents for the Direct Synthesis of Unsymmetrical Ketones. Cherney, A. H.; Reisman, S. E. Tetrahedron. 2013, 70, 3259. DOI: ​10.1016/j.tet.2013.11.104.
25. Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters. Repka, L. M.; Reisman, S. E. ​J. Org. Chem. 2013, 78, 12314. DOI: ​10.1021/jo4017953.
24. A Unified Strategy to ent-Kauranoid Natural Products: Total Syntheses of (–)-Trichorabdal A and (–)-Longikaurin E. Yeoman, J. T. S.; Mak, V. W.; Reisman, S. E. J. Am. Chem. Soc. ​2013, 135, 11764. DOI: ​10.1021/ja406599a.
23. Catalytic Asymmetric Reductive Acyl Cross-Coupling: Synthesis of Enantioenriched Acyclic α,α-Disubstituted Ketones. Cherney, A. H.; Kadunce, N. T.; Reisman, S. E. ​J. Am. Chem. Soc. 2013, 135, 7442. DOI: ​10.1021/ja402922w.
22. α-Diazo-β-Ketonitriles: Uniquely Reactive Substrates for Arene and Alkene Cyclopropanation. Nani, R. R.; Reisman, S. E. ​J. Am. Chem. Soc. 2013, 135, 7304. DOI: ​10.1021/ja401610p.
21. Direct, Enantioselective Synthesis of Pyrroloindolines and Indolines From Simple Indole Derivatives. Wang, H.; Reisman, S. E. Tetrahedron. 2013, 69, 5622. DOI: ​10.1016/j.tet.2013.04.003.
20. Copper-catalyzed Diastereoselective Arylation of Tryptophan Derivatives: Total Synthesis of (+)-Naseseazines A and B. Kieffer, M. E.; Chuang, K. V.; Reisman, S. E. J. Am. Chem. Soc. 2013, 135, 5557. DOI: ​10.1021/ja4023557.
19. Catalytic Asymmetric Synthesis of Highly Substituted Pyrrolizidines. Lim, A. D.; Codelli, J. A.; Reisman, S. E. Chem. Sci. 2013, 4, 650. DOI: ​10.1039/C2SC21617E.
18. A Copper-Catalyzed Arylation of Tryptamines for the Direct Synthesis of Aryl Pyrroloindolines. Kieffer, M. E.; Chuang, K. V.; Reisman, S. E. Chem. Sci. 2012, 3, 3170. DOI: ​10.1039/C2SC20914D.
17. Rapid Construction of the Aza-Propellane Core of Acutumine via a Photochemical [2 + 2] Cycloaddition Reaction. Navarro, R.; Reisman, S. E. Org. Lett. 2012, 14, 4354. DOI: ​10.1021/ol3017963.
16. Enantioselective Synthesis of Tryptophan Derivatives by a Tandem Friedel–Crafts Conjugate Addition/Asymmetric Protonation Reaction. Kieffer, M. E.; Repka, L. M.; Reisman, S. E. J. Am. Chem. Soc. 2012, 134, 5131. DOI: ​10.1021/ja209390d.
15. Enantioselective Total Synthesis of (−)-Acetylaranotin, a Dihydrooxepine Epidithiodiketopiperazine. Codelli, J. A.; Puchlopek, A. L. A.; Reisman, S. E. J. Am. Chem. Soc. 2012, 134, 1930. DOI: 10.1021/ja209354e. This synthesis was featured in November C&E News Article, found here. 
14. Buchner and Beyond: Arene Cyclopropanation as Applied to Natural Product Total Synthesis. Reisman, S. E.; Nani, R. R.; Levin, S. Synlett. 2011, 17, 2437. DOI: ​10.1055/s-0031-128952.
 13. A Concise Total Synthesis of (–)-Maoecrystal Z. Cha, J. Y.; Yeoman, J. T. S.; Reisman, S. E. J. Am. Chem. Soc. 2011, 133, 14965. DOI: 10.1021/ja2073356. This synthesis was featured in a September 2011 post on Totally Synthetic, found here, and featured in Synfacts 2011, 12, 1271, which can be found here.
12. Short, Enantioselective Total Syntheses of (–)-8-Demethoxyrunanine and (–)-Cepharatines A, C, and D. Chuang, K. V.; Navarro, R.; Reisman, S. E. Angew. Chem. Int. Ed. 2011, 50, 9447. DOI: 10.1002/anie.201104487. This synthesis was featured in Synfacts. 2012, 8, 14, which can be ​found here.
11. Benzoquinone-Derived Sulfinyl Imines as Versatile Intermediates for Alkaloid Synthesis: Total Synthesis of (–)-3-Demethoxyerythratidinone. Chuang, K. V.; Navarro, R.; Reisman, S. E. Chem. Sci. 2011, 2 (6), 1086. DOI: ​10.1039/c1sc00095k.
10. Enantioselective Total Synthesis of (+)-Salvileucalin B. Levin, S.; Nani, R. R.; Reisman, S. E. J. Am. Chem. Soc. 2011, 133, 774. DOI: 10.1021/ja110192b. This synthesis was featured in the February 2011 issue of Chemistry World, found here, as well as Synfacts. 2011, 6, 590, which can be found on the Synfacts page ​here.
9. Enantioselective Synthesis of Pyrroloindolines by a Formal [3+2] Cycloaddition Reaction. Repka, L. M.; Ni, J.; Reisman, S. E. J. Am. Chem. Soc. 2010, 132, 14418. DOI: ​10.1021/ja107328g.
8. Rapid Assembly of the Salvileucalin B Norcaradiene Core. Levin, S.; Nani, R. R.; Reisman, S. E. Org. Lett. 2010, 12, 780. DOI: ​10.1021/ol902848k.
Graduate and Postdoctoral Research
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7. Welwitindolinone C Synthetic Studies. Construction of the Welwitindolinone Carbon Skeleton Via a Transannular Nitrone Cycloaddition. Freeman, D. B.; Holubec, A. A.; Weiss, M. W.; Dixon, J. A.; Kakefuda, A.; Ohtsuka, M.; Inoue, M.; Vaswani, R. G.; Ohki, H.; Doan, B. D.; Reisman, S. E.; Stoltz, B. M.; Day, J. J.; Tao, R. N.; Dieterich, N. A.; Wood. J. L. Tetrahedron. 2010, 66, 6647. DOI: 10.1016/j.tet.2010.04.131

6. Enantioselective Thiourea-Catalyzed Additions to Oxocarbenium Ions. Reisman, S. E.; Doyle, A. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2008, 130, 7198. DOI: 10.1021/ja801514m

5. Evolution of a Synthetic Strategy: Total Synthesis of (±) Welwitindolinone A Isonitrile. Reisman, S. E.; Ready, J. M.; Weiss, M. M.; Hasuoka, A.; Tamaki, K.; Ovaska, T. V.; Wood, J. L. J. Am. Chem. Soc. 2008, 130, 2087. DOI: 10.1021/ja076663z

4. Total Synthesis of (±) Welwitindolinone A Isonitrile. Reisman, S. E.; Ready, J. M.; Hasuoka, A.; Smith, C. J.; Wood, J. L. J. Am. Chem. Soc. 2006, 128, 1448. DOI: 10.1021/ja057640s

3. A Mild and Efficient Synthesis of Oxindoles: Progress toward the Synthesis of Welwitindolinone A Isonitrile. Ready, J. M.; Reisman, S. E.; Hirata, M.; Weiss, M. M.; Tamaki, K.; Ovaska, T. V.; Wood, J. L. Angew. Chem., Int. Ed. 2004, 43, 1270. DOI: 10.1002/anie.200353282
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2. Facile Approach to the Bicyclo[5.3.0]Decane Ring System; Efficient Synthesis of (±)-7-epi-b-Bulnesene. Kumar, J. S. R.; O'Sullivan, M. F.; Reisman, S. E.; Hulford, C. A.; Ovaska, T. V. Tetrahedron Lett. 2002, 43, 1939. DOI: 10.1016/S0040-4039(02)00171-5

1. Facile Entry to the Tetracyclic 5-7-6-3 Tigliane Ring System. Ovaska, T. V.; Reisman, S. E.; Flynn, M. A. Org. Lett. 2001, 3, 115. DOI: ​10.1021/ol006823a
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