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Taotao Ling, Ph.D. - Publications

Affiliations: 
2001 University of California, San Diego, La Jolla, CA 
Area:
Organic Chemistry
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Year Citation  Score
2024 Barras BJ, Ling T, Rivas F. Recent Advances in Chemistry and Antioxidant/Anticancer Biology of Monoterpene and Meroterpenoid Natural Product. Molecules (Basel, Switzerland). 29. PMID 38202861 DOI: 10.3390/molecules29010279  0.678
2022 Ling T, Boyd L, Rivas F. Triterpenoids as Reactive Oxygen Species Modulators of Cell Fate. Chemical Research in Toxicology. 35: 569-584. PMID 35312315 DOI: 10.1021/acs.chemrestox.1c00428  0.631
2020 Ling T, Hadi V, Bollinger J, Rivas F. Identification of rapid access to polycyclic systems via a base-catalyzed cascade cyclization reaction and their biological evaluation. Bioorganic Chemistry. 99: 103846. PMID 32334195 DOI: 10.1016/J.Bioorg.2020.103846  0.682
2019 Ling T, Miller DJ, Lang W, Griffith E, Rodríguez-Cortés A, El Ayachi I, Palacios G, Min J, Miranda-Carboni GA, Lee RE, Rivas F. Mechanistic insight on the mode of action of colletoic acid. Journal of Medicinal Chemistry. PMID 31294974 DOI: 10.1021/Acs.Jmedchem.9B00187  0.651
2019 Ling T, Lang WH, Maier J, Quintana Centurion M, Rivas F. Cytostatic and Cytotoxic Natural Products against Cancer Cell Models. Molecules (Basel, Switzerland). 24. PMID 31130671 DOI: 10.3390/Molecules24102012  0.689
2019 Ling T, Lang WH, Craig J, Potts MB, Budhraja A, Opferman J, Bollinger J, Maier J, Marsico TD, Rivas F. Studies of Jatrogossone A as a Reactive Oxygen Species Inducer in Cancer Cellular Models. Journal of Natural Products. PMID 31084028 DOI: 10.1021/Acs.Jnatprod.8B01087  0.682
2019 Ling T, Lang WH, Martinez-Montemayor MM, Rivas F. Development of ergosterol peroxide probes for cellular localisation studies. Organic & Biomolecular Chemistry. PMID 31025693 DOI: 10.1039/C9Ob00145J  0.67
2019 Martínez-Montemayor MM, Ling T, Suárez-Arroyo IJ, Ortiz-Soto G, Santiago-Negrón CL, Lacourt-Ventura MY, Valentín-Acevedo A, Lang WH, Rivas F. Identification of Biologically Active Compounds and Synthesis of Improved Derivatives That Confer Anti-cancer Activities . Frontiers in Pharmacology. 10: 115. PMID 30837881 DOI: 10.3389/Fphar.2019.00115  0.67
2019 Santiago CL, Rivas F, Ling T, Suarez-Arroyo IJ, Ortiz G, Lacourt MY, Valentin A, Lang WH, Martínez-Montemayor MM. Abstract 1869: Mechanistic evaluation of ergosterol peroxide onin vitrobreast cancer models Cancer Research. DOI: 10.1158/1538-7445.Sabcs18-1869  0.637
2018 Ling T, Maier J, Das S, Budhraja A, Bassett R, Potts MB, Shelat A, Rankovic Z, Opferman JT, Rivas F. Identification of substituted 5-membered heterocyclic compounds as potential anti-leukemic agents. European Journal of Medicinal Chemistry. 164: 391-398. PMID 30611980 DOI: 10.1016/J.Ejmech.2018.12.059  0.68
2018 Ling T, Lang W, Feng X, Das S, Maier J, Jeffries C, Shelat A, Rivas F. Novel vitexin-inspired scaffold against leukemia. European Journal of Medicinal Chemistry. 146: 501-510. PMID 29407975 DOI: 10.1016/J.Ejmech.2018.01.004  0.682
2016 Gautam LN, Ling T, Lang W, Rivas F. Anti-proliferative evaluation of monoterpene derivatives against leukemia. European Journal of Medicinal Chemistry. 113: 75-80. PMID 26922230 DOI: 10.1016/J.Ejmech.2016.02.034  0.649
2016 Ling T, Gautam LN, Griffith E, Das S, Lang W, Shadrick WR, Shelat A, Lee R, Rivas F. Synthesis and evaluation of colletoic acid core derivatives. European Journal of Medicinal Chemistry. 110: 126-132. PMID 26820555 DOI: 10.1016/J.Ejmech.2016.01.027  0.653
2016 Rivas F, Ling T. Advances toward the Synthesis of Functionalized γ-Lactams Organic Preparations and Procedures International. 48: 254-295. DOI: 10.1080/00304948.2016.1165059  0.656
2016 Ling T, Rivas F. All-carbon quaternary centers in natural products and medicinal chemistry: recent advances Tetrahedron. 72: 6729-6777. DOI: 10.1016/J.Tet.2016.09.002  0.629
2015 Ling T, Tran M, González MA, Gautam LN, Connelly M, Wood RK, Fatima I, Miranda-Carboni G, Rivas F. (+)-Dehydroabietylamine derivatives target triple-negative breast cancer. European Journal of Medicinal Chemistry. 102: 9-13. PMID 26241873 DOI: 10.1016/J.Ejmech.2015.07.034  0.647
2013 Zhai B, Clark J, Ling T, Connelly M, Medina-Bolivar F, Rivas F. Antimalarial evaluation of the chemical constituents of hairy root culture of Bixa orellana L. Molecules (Basel, Switzerland). 19: 756-66. PMID 24406786 DOI: 10.3390/Molecules19010756  0.659
2013 Ling T, Griffith E, Mitachi K, Rivas F. Scalable and divergent total synthesis of (+)-colletoic acid, a selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor. Organic Letters. 15: 5790-3. PMID 24175735 DOI: 10.1021/Ol402842U  0.69
2013 Hadi V, Hotard M, Ling T, Salinas YG, Palacios G, Connelly M, Rivas F. Evaluation of Jatropha isabelli natural products and their synthetic analogs as potential antimalarial therapeutic agents. European Journal of Medicinal Chemistry. 65: 376-80. PMID 23747806 DOI: 10.1016/J.Ejmech.2013.04.030  0.683
2012 Mitachi K, Salinas YG, Connelly M, Jensen N, Ling T, Rivas F. Synthesis and structure-activity relationship of disubstituted benzamides as a novel class of antimalarial agents. Bioorganic & Medicinal Chemistry Letters. 22: 4536-9. PMID 22727641 DOI: 10.1016/J.Bmcl.2012.05.124  0.678
2011 Ling T, Xu J, Smith R, Ali A, Cantrell CL, Theodorakis EA. Synthesis of (-)-callicarpenal, a potent arthropod-repellent. Tetrahedron. 67: 3023-3029. PMID 21643472 DOI: 10.1016/J.Tet.2011.02.078  0.643
2006 Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Tang W, Frederick MO, Chen DY, Li Y, Ling T, Yamada YM. Total synthesis and structural elucidation of azaspiracid-1. Final assignment and total synthesis of the correct structure of azaspiracid-1. Journal of the American Chemical Society. 128: 2859-72. PMID 16506764 DOI: 10.1021/Ja054750Q  0.547
2006 Nicolaou KC, Chen DY, Li Y, Uesaka N, Petrovic G, Koftis TV, Bernal F, Frederick MO, Govindasamy M, Ling T, Pihko PM, Tang W, Vyskocil S. Total synthesis and structural elucidation of azaspiracid-1. Synthesis-based analysis of originally proposed structures and indication of their non-identity to the natural product. Journal of the American Chemical Society. 128: 2258-67. PMID 16478179 DOI: 10.1021/Ja054748Z  0.515
2006 Nicolaou K, Koftis T, Vyskocil S, Petrovic G, Tang W, Frederick M, Chen D, Ling T, Li Y, Yamada Y. Synthesis and Structural Elucidation of Azaspiracid-1 Synfacts. 2006: 0748-0748. DOI: 10.1055/S-2006-941937  0.414
2006 Ito E, Frederick MO, Koftis TV, Tang W, Petrovic G, Ling T, Nicolaou KC. Structure toxicity relationships of synthetic azaspiracid-1 and analogs in mice Harmful Algae. 5: 586-591. DOI: 10.1016/J.Hal.2005.11.005  0.405
2004 Nicolaou KC, Chen DY, Huang X, Ling T, Bella M, Snyder SA. Chemistry and biology of diazonamide A: first total synthesis and confirmation of the true structure. Journal of the American Chemical Society. 126: 12888-96. PMID 15469286 DOI: 10.1021/Ja040092I  0.462
2004 Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Ling T, Yamada YM, Tang W, Frederick MO. Structural revision and total synthesis of azaspiracid-1, part 2: definition of the ABCD domain and total synthesis. Angewandte Chemie (International Ed. in English). 43: 4318-24. PMID 15368381 DOI: 10.1002/Anie.200460696  0.391
2004 Nicolaou KC, Vyskocil S, Koftis TV, Yamada YM, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Structural revision and total synthesis of azaspiracid-1, part 1: intelligence gathering and tentative proposal. Angewandte Chemie (International Ed. in English). 43: 4312-8. PMID 15368380 DOI: 10.1002/Anie.200460695  0.47
2004 Nicolaou KC, Chen DY, Huang X, Ling T, Bella M, Snyder SA. Chemistry and Biology of Diazonamide A:  First Total Synthesis and Confirmation of the True Structure [J. Am. Chem. Soc.2004,126, 12888−12896]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja040823E  0.461
2004 Theodorakis EA, Ling T, Rueden EJ, Poupon E, Kim SH. Chapter 4 Quinone sesquiterpenes: A challenge for the development of a new synthetic methodology Strategies and Tactics in Organic Synthesis. 5: 111-131. DOI: 10.1016/S1874-6004(04)80027-3  0.658
2004 Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Cover Picture: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. Int. Ed. 33/2004) Angewandte Chemie International Edition. 43: 4239-4239. DOI: 10.1002/Anie.200490111  0.465
2004 Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Titelbild: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. 33/2004) Angewandte Chemie. 116: 4335-4335. DOI: 10.1002/Ange.200490110  0.472
2003 Lam T, Ling T, Chowdhury C, Chao TH, Bahjat FR, Lloyd GK, Moldawer LL, Palladino MA, Theodorakis EA. Synthesis of a novel family of diterpenes and their evaluation as anti-inflammatory agents. Bioorganic & Medicinal Chemistry Letters. 13: 3217-21. PMID 12951096 DOI: 10.1016/S0960-894X(03)00669-3  0.77
2003 Nicolaou KC, Chen DY, Li Y, Qian W, Ling T, Vyskocil S, Koftis TV, Govindasamy M, Uesaka N. Total synthesis of the proposed azaspiracid-1 structure, part 2: coupling of the C1-C20, C21-C27, and C28-C40 fragments and completion of the synthesis. Angewandte Chemie (International Ed. in English). 42: 3649-53. PMID 12916037 DOI: 10.1002/Anie.200351826  0.411
2003 Nicolaou KC, Li Y, Uesaka N, Koftis TV, Vyskocil S, Ling T, Govindasamy M, Qian W, Bernal F, Chen DY. Total synthesis of the proposed azaspiracid-1 structure, part 1: construction of the enantiomerically pure C1-C20, C21-C27, and C28-C40 fragments. Angewandte Chemie (International Ed. in English). 42: 3643-8. PMID 12916036 DOI: 10.1002/Anie.200351825  0.482
2002 Ling T, Poupon E, Rueden EJ, Kim SH, Theodorakis EA. Unified synthesis of quinone sesquiterpenes based on a radical decarboxylation and quinone addition reaction. Journal of the American Chemical Society. 124: 12261-7. PMID 12371868 DOI: 10.1021/Ja027517Q  0.64
2002 Nicolaou KC, Bella M, Chen DY, Huang X, Ling T, Snyder SA. Total synthesis of diazonamide A. Angewandte Chemie (International Ed. in English). 41: 3495-9. PMID 12298077 DOI: 10.1002/1521-3773(20020916)41:18<3495::Aid-Anie3495>3.0.Co;2-7  0.496
2002 Ling T, Poupon E, Rueden EJ, Theodorakis EA. Synthesis of (-)-ilimaquinone via a radical decarboxylation and quinone addition reaction. Organic Letters. 4: 819-22. PMID 11869136 DOI: 10.1021/Ol025501Z  0.603
2002 Ling T, Rivas F, Theodorakis EA. Stereoselective synthesis of the fully functionalized core fragment of terpentecin Tetrahedron Letters. 43: 9019-9022. DOI: 10.1016/S0040-4039(02)02314-6  0.742
2001 Ling T, Chowdhury C, Kramer BA, Vong BG, Palladino MA, Theodorakis EA. Enantioselective synthesis of the antiinflammatory agent (-)-acanthoic acid. The Journal of Organic Chemistry. 66: 8843-53. PMID 11749614 DOI: 10.1021/Jo0159035  0.768
2001 Haidekker MA, Ling T, Anglo M, Stevens HY, Frangos JA, Theodorakis EA. New fluorescent probes for the measurement of cell membrane viscosity. Chemistry & Biology. 8: 123-31. PMID 11251287 DOI: 10.1016/S1074-5521(00)90061-9  0.515
2000 Ling T, Kramer BA, Palladino MA, Theodorakis EA. Stereoselective synthesis of (-)-acanthoic acid. Organic Letters. 2: 2073-6. PMID 10891233 DOI: 10.1021/Ol0060578  0.642
2000 Drouet KE, Ling T, Tran HV, Theodorakis EA. Enantioselective synthesis of the [6,6] spiroketal core of reveromycin A. Organic Letters. 2: 207-10. PMID 10814283 DOI: 10.1021/Ol991290V  0.633
1999 Ling T, Xiang AX, Theodorakis EA. Enantioselective Total Synthesis of Avarol and Avarone. Angewandte Chemie (International Ed. in English). 38: 3089-3091. PMID 10540432 DOI: 10.1002/(Sici)1521-3773(19991018)38:20<3089::Aid-Anie3089>3.0.Co;2-W  0.775
1999 Ling T, Xiang AX, Theodorakis EA. Enantioselektive Totalsynthese von Avarol und Avaron Angewandte Chemie. 111: 3277-3279. DOI: 10.1002/(Sici)1521-3757(19991018)111:20<3277::Aid-Ange3277>3.0.Co;2-M  0.712
1998 Xiang AX, Watson DA, Ling T, Theodorakis EA. Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology. The Journal of Organic Chemistry. 63: 6774-6775. PMID 11672290 DOI: 10.1021/Jo981331L  0.787
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