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Thomas J. Maimone, Ph.D. - Publications

Affiliations: 
Chemistry University of California, Berkeley, Berkeley, CA, United States 
Area:
Organic Chemistry, Organometallic Chemistry, Catalysis
Website:
http://www.cchem.berkeley.edu/tjm/Lab_website/Home.html
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58 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Gowans FA, Thach DQ, Zhu Z, Wang Y, Altamirano Poblano BE, Dovala D, Tallarico JA, McKenna JM, Schirle M, Maimone TJ, Nomura DK. Ophiobolin A Covalently Targets Mitochondrial Complex IV Leading to Metabolic Collapse in Cancer Cells. Acs Chemical Biology. PMID 38739449 DOI: 10.1021/acschembio.4c00064  0.501
2023 Harmange Magnani CS, Hernández-Meléndez JR, Tantillo DJ, Maimone TJ. Total Synthesis of Altemicidin: A Surprise Ending for a Monoterpene Alkaloid. Jacs Au. 3: 2883-2893. PMID 37885570 DOI: 10.1021/jacsau.3c00417  0.322
2023 Belcher BP, Machicao PA, Tong B, Ho E, Friedli J, So B, Bui H, Isobe Y, Maimone TJ, Nomura DK. Chemoproteomic Profiling Reveals that Anti-Cancer Natural Product Dankastatin B Covalently Targets Mitochondrial VDAC3. Chembiochem : a European Journal of Chemical Biology. e202300111. PMID 36964942 DOI: 10.1002/cbic.202300111  0.543
2023 Gowans FA, Thach DQ, Wang Y, Altamirano Poblano BE, Dovala D, Tallarico JA, McKenna JM, Schirle M, Maimone TJ, Nomura DK. Ophiobolin A Covalently Targets Complex IV Leading to Mitochondrial Metabolic Collapse in Cancer Cells. Biorxiv : the Preprint Server For Biology. PMID 36945520 DOI: 10.1101/2023.03.09.531918  0.512
2023 Belcher BP, Machicao PA, Tong B, Ho E, Friedli J, So B, Bui H, Isobe Y, Maimone TJ, Nomura DK. Chemoproteomic Profiling Reveals that Anti-Cancer Natural Product Dankastatin B Covalently Targets Mitochondrial VDAC3. Biorxiv : the Preprint Server For Biology. PMID 36798342 DOI: 10.1101/2023.02.11.528139  0.542
2021 Tong B, Belcher BP, Nomura DK, Maimone TJ. Chemical investigations into the biosynthesis of the gymnastatin and dankastatin alkaloids. Chemical Science. 12: 8884-8891. PMID 34257889 DOI: 10.1039/d1sc02613e  0.685
2021 Cho H, Shen Q, Zhang LH, Okumura M, Kawakami A, Ambrose J, Sigoillot F, Miller HR, Gleim S, Cobos-Correa A, Wang Y, Piechon P, Roma G, Eggimann F, Moore C, ... ... Maimone TJ, et al. CYP27A1-dependent anti-melanoma activity of limonoid natural products targets mitochondrial metabolism. Cell Chemical Biology. PMID 33794192 DOI: 10.1016/j.chembiol.2021.03.004  0.508
2021 Luo M, Spradlin JN, Boike L, Tong B, Brittain SM, McKenna JM, Tallarico JA, Schirle M, Maimone TJ, Nomura DK. Chemoproteomics-enabled discovery of covalent RNF114-based degraders that mimic natural product function. Cell Chemical Biology. PMID 33513350 DOI: 10.1016/j.chembiol.2021.01.005  0.563
2021 Shen X, Thach DQ, Ting CP, Maimone TJ. Annulative Methods in the Synthesis of Complex Meroterpene Natural Products. Accounts of Chemical Research. PMID 33448794 DOI: 10.1021/acs.accounts.0c00781  0.338
2020 Tong B, Luo M, Xie Y, Spradlin JN, Tallarico JA, McKenna JM, Schirle M, Maimone TJ, Nomura DK. Bardoxolone conjugation enables targeted protein degradation of BRD4. Scientific Reports. 10: 15543. PMID 32968148 DOI: 10.1038/s41598-020-72491-9  0.504
2020 Isobe Y, Okumura M, McGregor LM, Brittain SM, Jones MD, Liang X, White R, Forrester W, McKenna JM, Tallarico JA, Schirle M, Maimone TJ, Nomura DK. Manumycin polyketides act as molecular glues between UBR7 and P53. Nature Chemical Biology. PMID 32572277 DOI: 10.1038/S41589-020-0557-2  0.578
2020 Tong B, Spradlin JN, Novaes LFT, Zhang E, Hu X, Moeller M, Brittain SM, McGregor LM, McKenna JM, Tallarico JA, Schirle M, Maimone TJ, Nomura DK. A Nimbolide-Based Kinase Degrader Preferentially Degrades Oncogenic BCR-ABL. Acs Chemical Biology. PMID 32568522 DOI: 10.1021/Acschembio.0C00348  0.555
2020 Harmange Magnani CS, Thach DQ, Haelsig KT, Maimone TJ. Syntheses of Complex Terpenes from Simple Polyprenyl Precursors. Accounts of Chemical Research. PMID 32202757 DOI: 10.1021/Acs.Accounts.0C00055  0.39
2020 Shen X, Ting CP, Xu G, Maimone TJ. Programmable meroterpene synthesis. Nature Communications. 11: 508. PMID 31980637 DOI: 10.1038/S41467-020-14354-5  0.415
2020 Haelsig KT, Xuan J, Maimone TJ. Total Synthesis of (-)-Curvulamine. Journal of the American Chemical Society. PMID 31899626 DOI: 10.1021/Jacs.9B12546  0.387
2019 Thach D, Brill Z, Grover H, Esguerra K, Thompson J, Maimone T. Total Synthesis of (+)-6-epi-Ophiobolin A. Angewandte Chemie (International Ed. in English). PMID 31693792 DOI: 10.1002/Anie.201913150  0.694
2019 Bersuker K, Hendricks J, Li Z, Magtanong L, Ford B, Tang PH, Roberts MA, Tong B, Maimone TJ, Zoncu R, Bassik MC, Nomura DK, Dixon SJ, Olzmann JA. The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis. Nature. PMID 31634900 DOI: 10.1038/S41586-019-1705-2  0.531
2019 Hu X, Musacchio AJ, Shen X, Tao Y, Maimone TJ. Allylative Approaches to the Synthesis of Complex Guaianolide Sesquiterpenes from and . Journal of the American Chemical Society. PMID 31448610 DOI: 10.1021/Jacs.9B08001  0.403
2019 Spradlin JN, Hu X, Ward CC, Brittain SM, Jones MD, Ou L, To M, Proudfoot A, Ornelas E, Woldegiorgis M, Olzmann JA, Bussiere DE, Thomas JR, Tallarico JA, McKenna JM, ... ... Maimone TJ, et al. Harnessing the anti-cancer natural product nimbolide for targeted protein degradation. Nature Chemical Biology. PMID 31209351 DOI: 10.1038/S41589-019-0304-8  0.582
2019 Berdan CA, Ho R, Lehtola HS, To M, Hu X, Huffman TR, Petri Y, Altobelli CR, Demeulenaere SG, Olzmann JA, Maimone TJ, Nomura DK. Parthenolide Covalently Targets and Inhibits Focal Adhesion Kinase in Breast Cancer Cells. Cell Chemical Biology. PMID 31080076 DOI: 10.1016/J.Chembiol.2019.03.016  0.564
2019 Hung K, Condakes ML, Novaes LFT, Harwood S, Morikawa T, Yang Z, Maimone TJ. Development of a Terpene Feedstock-based Oxidative Synthetic Approach to the Illicium Sesquiterpenes. Journal of the American Chemical Society. PMID 30698435 DOI: 10.1021/Jacs.8B12247  0.405
2019 Condakes M, Rosen RZ, Harwood SJ, Maimone TJ. A copper-catalyzed double coupling enables a 3-step synthesis of the quassinoid core architecture Chemical Science. 10: 768-772. DOI: 10.1039/C8Sc03835J  0.332
2019 Brill ZG, Zhao Y, Vasilev VH, Maimone TJ. Synthetic approaches to the daphnane and tigliane diterpenes from aromatic precursors Tetrahedron. 75: 4212-4221. DOI: 10.1016/J.Tet.2019.04.058  0.388
2019 Ting CP, Tschanen E, Jang E, Maimone TJ. Total synthesis of podophyllotoxin and select analog designs via C–H activation Tetrahedron. 75: 3299-3308. DOI: 10.1016/J.Tet.2019.04.052  0.419
2019 Tong B, Maimone TJ. Enlightening Terpene Synthesis Chem. 5: 1368-1370. DOI: 10.1016/J.Chempr.2019.05.002  0.313
2018 Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, Henderson MJ, Lynch C, Zhao T, Wan KK, Itkin Z, Dillon C, Shen M, Cheff DM, Lee TD, Bougie D, Cheng K, Coussens NP, ... ... Maimone TJ, et al. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741. PMID 30648156 DOI: 10.1021/Acscentsci.8B00747  0.743
2018 Hu X, Lim P, Fairhurst RM, Maimone TJ. Synthesis and Study of the Antimalarial Cardamom Peroxide. Tetrahedron. 74: 3358-3369. PMID 30319159 DOI: 10.1016/J.Tet.2018.03.045  0.352
2018 Nomura DK, Maimone TJ. Target Identification of Bioactive Covalently Acting Natural Products. Current Topics in Microbiology and Immunology. PMID 30105423 DOI: 10.1007/82_2018_121  0.6
2018 Hung K, Hu X, Maimone TJ. Total synthesis of complex terpenoids employing radical cascade processes. Natural Product Reports. PMID 29417970 DOI: 10.1039/C7Np00065K  0.387
2017 Condakes ML, Hung K, Harwood S, Maimone TJ. Total Syntheses of (-)-Majucin and (-)-Jiadifenoxolane A, Complex Majucin-Type Illicium Sesquiterpenes. Journal of the American Chemical Society. PMID 29148748 DOI: 10.1021/Jacs.7B11493  0.339
2017 Xu G, Elkin M, Tantillo D, Newhouse T, Maimone T. Traversing Biosynthetic Carbocation Landscapes in the Total Synthesis of Andrastin and Terretonin Meroterpenes. Angewandte Chemie (International Ed. in English). PMID 28799296 DOI: 10.1002/Anie.201705654  0.666
2017 Brill ZG, Condakes ML, Ting CP, Maimone TJ. Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products. Chemical Reviews. PMID 28293944 DOI: 10.1021/Acs.Chemrev.6B00834  0.384
2017 Hu X, Xu S, Maimone TJ. A Double Allylation Strategy for Gram-Scale Guaianolide Production: Total Synthesis of (+)-Mikanokryptin. Angewandte Chemie (International Ed. in English). PMID 28052523 DOI: 10.1002/Anie.201611078  0.399
2016 Hung K, Condakes M, Morikawa T, Maimone TJ. Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin. Journal of the American Chemical Society. PMID 27966918 DOI: 10.1021/Jacs.6B11739  0.363
2016 Ting CP, Xu G, Zeng X, Maimone TJ. Annulative Methods Enable a Total Synthesis of the Complex Meroterpene Berkeleyone A. Journal of the American Chemical Society. PMID 27809506 DOI: 10.1021/Jacs.6B10397  0.399
2016 Brill ZG, Grover HK, Maimone TJ. Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade. Science (New York, N.Y.). 352: 1078-82. PMID 27230373 DOI: 10.1126/Science.Aaf6742  0.397
2016 Maimone T, Ting C. The Total Synthesis of Hyperforin Synlett. 27: 1443-1449. DOI: 10.1055/S-0035-1561619  0.373
2015 Ting CP, Maimone TJ. Total Synthesis of Hyperforin. Journal of the American Chemical Society. PMID 26252484 DOI: 10.1021/Jacs.5B06939  0.414
2015 Maimone TJ, Ishihara Y, Baran PS. Scalable Total Syntheses of (-)-Hapalindole U and (+)-Ambiguine H. Tetrahedron. 71: 3652-3665. PMID 25983347 DOI: 10.1016/J.Tet.2014.11.010  0.65
2015 Zhao YM, Maimone TJ. Short, enantioselective total synthesis of chatancin. Angewandte Chemie (International Ed. in English). 54: 1223-6. PMID 25470723 DOI: 10.1002/Anie.201410443  0.385
2014 Hu X, Maimone TJ. Four-step synthesis of the antimalarial cardamom peroxide via an oxygen stitching strategy. Journal of the American Chemical Society. 136: 5287-90. PMID 24673099 DOI: 10.1021/Ja502208Z  0.323
2014 Ting CP, Maimone TJ. C-H bond arylation in the synthesis of aryltetralin lignans: a short total synthesis of podophyllotoxin. Angewandte Chemie (International Ed. in English). 53: 3115-9. PMID 24519950 DOI: 10.1002/Anie.201311112  0.351
2014 Carreira EM, Westphal M, Ting CP, Maimone TJ. Synthesis of Podophyllotoxin Synfacts. 10: 457-457. DOI: 10.1055/S-0033-1341095  0.344
2012 Milner PJ, Maimone TJ, Su M, Chen J, Müller P, Buchwald SL. Investigating the dearomative rearrangement of biaryl phosphine-ligated Pd(II) complexes. Journal of the American Chemical Society. 134: 19922-34. PMID 23153301 DOI: 10.1021/Ja310351E  0.693
2012 Krenske EH, Perry EW, Jerome SV, Maimone TJ, Baran PS, Houk KN. Why a proximity-induced Diels-Alder reaction is so fast. Organic Letters. 14: 3016-9. PMID 22630569 DOI: 10.1021/Ol301083Q  0.487
2011 Maimone TJ, Milner PJ, Kinzel T, Zhang Y, Takase MK, Buchwald SL. Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides. Journal of the American Chemical Society. 133: 18106-9. PMID 21999801 DOI: 10.1021/Ja208461K  0.659
2011 Noël T, Maimone TJ, Buchwald SL. Accelerating palladium-catalyzed C-F bond formation: use of a microflow packed-bed reactor. Angewandte Chemie (International Ed. in English). 50: 8900-3. PMID 21837710 DOI: 10.1002/Anie.201104652  0.589
2010 Maimone TJ, Buchwald SL. Pd-catalyzed O-arylation of ethyl acetohydroximate: synthesis of O-arylhydroxylamines and substituted benzofurans. Journal of the American Chemical Society. 132: 9990-1. PMID 20604520 DOI: 10.1021/Ja1044874  0.446
2010 Maimone TJ, Shi J, Ashida S, Baran PS. Synthesis of Vinigrol Synfacts. 2010: 259-259. DOI: 10.1055/S-0029-1219247  0.524
2009 Maimone TJ, Shi J, Ashida S, Baran PS. Total synthesis of vinigrol. Journal of the American Chemical Society. 131: 17066-7. PMID 19877628 DOI: 10.1021/Ja908194B  0.525
2008 Maimone TJ, Voica AF, Baran PS. A concise approach to vinigrol. Angewandte Chemie (International Ed. in English). 47: 3054-6. PMID 18338349 DOI: 10.1002/Anie.200800167  0.693
2008 Maimone T, Voica A, Baran P. Ein einfacher Zugang zu Vinigrol Angewandte Chemie. 120: 3097-3099. DOI: 10.1002/Ange.200800167  0.682
2007 Malerich JP, Maimone TJ, Elliott GI, Trauner D. Biomimetic Synthesis of Antimalarial Naphthoquinones. Journal of the American Chemical Society. 129: 1836. PMID 27518592 DOI: 10.1021/Ja069018L  0.488
2007 Richter JM, Whitefield BW, Maimone TJ, Lin DW, Castroviejo MP, Baran PS. Scope and mechanism of direct indole and pyrrole couplings adjacent to carbonyl compounds: total synthesis of acremoauxin A and oxazinin 3. Journal of the American Chemical Society. 129: 12857-69. PMID 17900115 DOI: 10.1021/Ja074392M  0.678
2007 Maimone TJ, Baran PS. Modern synthetic efforts toward biologically active terpenes. Nature Chemical Biology. 3: 396-407. PMID 17576427 DOI: 10.1038/Nchembio.2007.1  0.561
2007 Baran PS, Maimone TJ, Richter JM. Total synthesis of marine natural products without using protecting groups. Nature. 446: 404-8. PMID 17377577 DOI: 10.1038/Nature05569  0.688
2007 Baran PS, Maimone TJ. Organic chemistry: a tuxedo for iodine atoms. Nature. 445: 826-7. PMID 17314962 DOI: 10.1038/445826A  0.466
2005 Malerich JP, Maimone TJ, Elliott GI, Trauner D. Biomimetic synthesis of antimalarial naphthoquinones. Journal of the American Chemical Society. 127: 6276-83. PMID 15853334 DOI: 10.1021/Ja050092Y  0.5
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