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Timothy F. Jamison - Publications

Affiliations: 
1999- Chemistry Massachusetts Institute of Technology, Cambridge, MA, United States 
Area:
organic synthesis
Website:
http://chemistry.mit.edu/professor-timothy-f-jamison

129 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
2021 Gopalsamuthiram V, Kadam AL, Noble JK, Snead DR, Williams C, Jamison TF, Senanayake C, Yadaw AK, Roy S, Sirasani G, Gupton BF, Burns J, Cook DW, Stringham RW, Ahmad S, et al. Toward a Practical, Nonenzymatic Process for Investigational COVID-19 Antiviral Molnupiravir from Cytidine: Supply-Centered Synthesis. Organic Process Research & Development. 25: 2679-2685. PMID 34955627 DOI: 10.1021/acs.oprd.1c00219  0.304
2021 Fu WC, MacQueen PM, Jamison TF. Continuous flow strategies for using fluorinated greenhouse gases in fluoroalkylations. Chemical Society Reviews. PMID 34018500 DOI: 10.1039/d0cs00670j  0.775
2020 Danahy KE, Styduhar ED, Fodness AM, Heckman LM, Jamison TF. On-Demand Generation and Use in Continuous Synthesis of the Ambiphilic Nitrogen Source Chloramine. Organic Letters. PMID 33086788 DOI: 10.1021/acs.orglett.0c03021  0.811
2020 Fu WC, Jamison TF. Deuteriodifluoromethylation and gem-Difluoroalkenylation of Aldehydes Using ClCF H in Continuous Flow. Angewandte Chemie (International Ed. in English). PMID 32495996 DOI: 10.1002/Anie.202004260  0.764
2019 Seo H, Jamison TF. Catalytic Generation and Use of Ketyl Radical from Unactivated Aliphatic Carbonyl Compounds. Organic Letters. PMID 31820654 DOI: 10.1021/Acs.Orglett.9B04235  0.414
2019 Breen CP, Jamison TF. Continuous Flow Synthesis of ACE Inhibitors From N-Substituted l-Alanine Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31625640 DOI: 10.1002/Chem.201904400  0.423
2019 Kelley EH, Jamison TF. Synthesis of the Framework of Tamulamides A and B. Organic Letters. PMID 31523969 DOI: 10.1021/Acs.Orglett.9B03015  0.367
2019 Coley CW, Thomas DA, Lummiss JAM, Jaworski JN, Breen CP, Schultz V, Hart T, Fishman JS, Rogers L, Gao H, Hicklin RW, Plehiers PP, Byington J, Piotti JS, Green WH, ... ... Jamison TF, et al. A robotic platform for flow synthesis of organic compounds informed by AI planning. Science (New York, N.Y.). 365. PMID 31395756 DOI: 10.1126/Science.Aax1566  0.387
2019 Fu WC, Jamison TF. Modular Continuous Flow Synthesis of Imatinib and Analogues. Organic Letters. PMID 31314541 DOI: 10.1021/Acs.Orglett.9B02259  0.782
2019 McGeough CP, Strom AE, Jamison TF. Ni-Catalyzed Cross-Electrophile Coupling for the Synthesis of Skipped Polyenes. Organic Letters. PMID 31046296 DOI: 10.1021/Acs.Orglett.9B01019  0.412
2019 Russell MG, Jamison TF. Seven-Step Continuous Flow Synthesis of Linezolid Without Intermediate Purification. Angewandte Chemie (International Ed. in English). PMID 30964955 DOI: 10.1002/Anie.201901814  0.443
2019 Bedermann AA, McTeague TA, Jamison TF. Automated On-Demand Titration of Organometallic Reagents in Continuous Flow Organic Process Research & Development. 23: 278-282. DOI: 10.1021/Acs.Oprd.8B00434  0.416
2018 Ziegler RE, Desai BK, Jee JA, Gupton BF, Roper TD, Jamison TF. Corrigendum: 7-Step Flow Synthesis of the HIV Integrase Inhibitor Dolutegravir. Angewandte Chemie (International Ed. in English). 57: 14969. PMID 30398024 DOI: 10.1002/Anie.201809594  0.32
2018 Bédard AC, Adamo A, Aroh KC, Russell MG, Bedermann AA, Torosian J, Yue B, Jensen KF, Jamison TF. Reconfigurable system for automated optimization of diverse chemical reactions. Science (New York, N.Y.). 361: 1220-1225. PMID 30237351 DOI: 10.1126/Science.Aat0650  0.376
2018 Gates ZP, Vinogradov AA, Quartararo AJ, Bandyopadhyay A, Choo ZN, Evans ED, Halloran KH, Mijalis AJ, Mong SK, Simon MD, Standley EA, Styduhar ED, Tasker SZ, Touti F, Weber JM, ... ... Jamison TF, et al. Xenoprotein engineering via synthetic libraries. Proceedings of the National Academy of Sciences of the United States of America. PMID 29784819 DOI: 10.1073/Pnas.1722633115  0.757
2018 Heckman LM, He Z, Jamison TF. Synthesis of Highly Substituted 2-Arylindoles via Copper-Catalyzed Coupling of Isocyanides and Arylboronic Acids. Organic Letters. PMID 29761699 DOI: 10.1021/Acs.Orglett.8B01132  0.447
2018 Ziegler RE, Desai BK, Jee JA, Gupton BF, Roper TD, Jamison TF. 7-Step Flow Synthesis of the HIV Integrase Inhibitor Dolutegravir. Angewandte Chemie (International Ed. in English). PMID 29756689 DOI: 10.1002/Anie.201802256  0.383
2018 Kelley EH, Jamison TF. Synthesis of the ABC framework of tamulamides A and B. Bioorganic & Medicinal Chemistry. PMID 29729986 DOI: 10.1016/J.Bmc.2018.04.046  0.371
2018 Katcher M, Jamison TF. Studies toward brevisulcenal F via convergent strategies for marine ladder polyether synthesis. Tetrahedron. 74: 1111-1122. PMID 29479119 DOI: 10.1016/J.Tet.2018.01.039  0.804
2018 Li H, Breen CP, Seo H, Jamison TF, Fang YQ, Bio MM. Ni-Catalyzed Electrochemical Decarboxylative C-C Couplings in Batch and Continuous Flow. Organic Letters. PMID 29431449 DOI: 10.1021/Acs.Orglett.8B00070  0.428
2018 Zhang P, Weeranoppanant N, Thomas DA, Tahara K, Stelzer T, Russell MG, O'Mahony M, Myerson AS, Lin H, Kelly LP, Jensen KF, Jamison TF, Dai C, Cui Y, Briggs N, et al. Advanced Continuous Flow Platform for On-Demand Pharmaceutical Manufacturing. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29385292 DOI: 10.1002/Chem.201706004  0.556
2018 Leibfarth FA, Russell MG, Langley DM, Seo H, Kelly LP, Carney DW, Sello JK, Jamison TF. Continuous-Flow Chemistry in Undergraduate Education: Sustainable Conversion of Reclaimed Vegetable Oil into Biodiesel Journal of Chemical Education. 95: 1371-1375. DOI: 10.1021/Acs.Jchemed.7B00719  0.774
2018 Ziegler RE, Desai BK, Jee J, Gupton BF, Roper TD, Jamison TF. Berichtigung: 7‐Step Flow Synthesis of the HIV Integrase Inhibitor Dolutegravir Angewandte Chemie. 130: 15185-15185. DOI: 10.1002/Ange.201809594  0.302
2017 Seo H, Liu A, Jamison TF. Direct β-Selective Hydrocarboxylation of Styrenes with CO2 Enabled by Continuous Flow Photoredox Catalysis. Journal of the American Chemical Society. PMID 28953365 DOI: 10.1021/Jacs.7B05942  0.318
2017 Morse PD, Jamison TF. Synthesis and Utilization of Nitroalkyne Equivalents in Batch and Continuous Flow. Angewandte Chemie (International Ed. in English). PMID 28929565 DOI: 10.1002/Anie.201706157  0.505
2017 Lin H, Dai C, Jamison TF, Jensen KF. A Rapid Total Synthesis of Ciprofloxacin Hydrochloride in Continuous Flow. Angewandte Chemie (International Ed. in English). PMID 28561939 DOI: 10.1002/Anie.201703812  0.632
2017 Britton J, Jamison TF. A Unified Continuous Flow Assembly Line Synthesis of Highly Substituted Pyrazoles and Pyrazolines. Angewandte Chemie (International Ed. in English). PMID 28544160 DOI: 10.1002/Anie.201704529  0.465
2017 Seo H, Katcher MH, Jamison TF. Photoredox activation of carbon dioxide for amino acid synthesis in continuous flow. Nature Chemistry. 9: 453-456. PMID 28430203 DOI: 10.1038/Nchem.2690  0.788
2017 Bédard AC, Longstreet AR, Britton J, Wang Y, Moriguchi H, Hicklin RW, Green WH, Jamison TF. Minimizing E-factor in the continuous-flow synthesis of diazepam and atropine. Bioorganic & Medicinal Chemistry. PMID 28284869 DOI: 10.1016/J.Bmc.2017.02.002  0.365
2017 Lummiss JA, Morse PD, Beingessner RL, Jamison TF. Towards More Efficient, Greener Syntheses Through Flow Chemistry. Chemical Record (New York, N.Y.). PMID 28245339 DOI: 10.1002/Tcr.201600139  0.453
2017 Wicker AC, Leibfarth FA, Jamison TF. Flow-IEG enables programmable thermodynamic properties in sequence-defined unimolecular macromolecules Polymer Chemistry. 8: 5786-5794. DOI: 10.1039/C7Py01204G  0.717
2016 McTeague TA, Jamison TF. Photoredox Activation of SF6 for Fluorination. Angewandte Chemie (International Ed. in English). PMID 27813242 DOI: 10.1002/Anie.201608792  0.416
2016 Adamo A, Beingessner RL, Behnam M, Chen J, Jamison TF, Jensen KF, Monbaliu JC, Myerson AS, Revalor EM, Snead DR, Stelzer T, Weeranoppanant N, Wong SY, Zhang P. On-demand continuous-flow production of pharmaceuticals in a compact, reconfigurable system. Science (New York, N.Y.). 352: 61-7. PMID 27034366 DOI: 10.1126/Science.Aaf1337  0.396
2016 Haimov E, Nairoukh Z, Shterenberg A, Berkovitz T, Jamison TF, Marek I. Stereoselective Formation of Fully Substituted Ketone Enolates. Angewandte Chemie (International Ed. in English). PMID 27027778 DOI: 10.1002/Anie.201601883  0.418
2016 Morse PD, Beingessner RL, Jamison TF. Enhanced Reaction Efficiency in Continuous Flow Israel Journal of Chemistry. 57: 218-227. DOI: 10.1002/Ijch.201600095  0.424
2015 Barnes JC, Ehrlich DJ, Gao AX, Leibfarth FA, Jiang Y, Zhou E, Jamison TF, Johnson JA. Iterative exponential growth of stereo- and sequence-controlled polymers. Nature Chemistry. 7: 810-5. PMID 26391080 DOI: 10.1038/Nchem.2346  0.677
2015 Leibfarth FA, Johnson JA, Jamison TF. Scalable synthesis of sequence-defined, unimolecular macromolecules by Flow-IEG. Proceedings of the National Academy of Sciences of the United States of America. 112: 10617-22. PMID 26269573 DOI: 10.1073/Pnas.1508599112  0.722
2015 Armbrust KW, Beaver MG, Jamison TF. Rhodium-catalyzed endo-selective epoxide-opening cascades: formal synthesis of (-)-brevisin. Journal of the American Chemical Society. 137: 6941-6. PMID 25984951 DOI: 10.1021/Jacs.5B03570  0.801
2015 Standley EA, Tasker SZ, Jensen KL, Jamison TF. Nickel Catalysis: Synergy between Method Development and Total Synthesis. Accounts of Chemical Research. 48: 1503-14. PMID 25905431 DOI: 10.1021/Acs.Accounts.5B00064  0.486
2015 Jensen KL, Nielsen DU, Jamison TF. A General Strategy for the Synthesis of Enantiomerically Pure Azetidines and Aziridines through Nickel-Catalyzed Cross-Coupling. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7379-83. PMID 25820027 DOI: 10.1002/Chem.201500886  0.441
2015 Starkov P, Jamison TF, Marek I. Electrophilic amination: the case of nitrenoids. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5278-300. PMID 25641706 DOI: 10.1002/Chem.201405779  0.323
2015 Snead DR, Jamison TF. A three-minute synthesis and purification of ibuprofen: pushing the limits of continuous-flow processing. Angewandte Chemie (International Ed. in English). 54: 983-7. PMID 25470733 DOI: 10.1002/Anie.201409093  0.391
2015 Dai C, Snead DR, Zhang P, Jamison TF. Continuous-flow synthesis and purification of atropine with sequential in-line separations of structurally similar impurities Journal of Flow Chemistry. 5: 133-138. DOI: 10.1556/1846.2015.00013  0.549
2015 Leibfarth FA, Johnson JA, Jamison TF. Scalable synthesis of sequence-defined, unimolecular macromolecules by Flow-IEG Proceedings of the National Academy of Sciences of the United States of America. 112: 10617-10622. DOI: 10.1073/pnas.1508599112  0.69
2015 Knochel P, Fernandez S, Jensen KL, Nielsen DU, Jamison TF. Asymetric Nickel-Catalyzed Synthesis of Azetidines and Aziridines Synfacts. 11: 755-755. DOI: 10.1055/S-0034-1380906  0.445
2014 Andrade LH, Kroutil W, Jamison TF. Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP. Organic Letters. 16: 6092-5. PMID 25394227 DOI: 10.1021/Ol502712V  0.38
2014 He Z, Bae M, Wu J, Jamison TF. Synthesis of highly functionalized polycyclic quinoxaline derivatives using visible-light photoredox catalysis. Angewandte Chemie (International Ed. in English). 53: 14451-5. PMID 25347967 DOI: 10.1002/Anie.201408522  0.422
2014 Jensen KL, Standley EA, Jamison TF. Highly regioselective nickel-catalyzed cross-coupling of N-tosylaziridines and alkylzinc reagents. Journal of the American Chemical Society. 136: 11145-52. PMID 25055180 DOI: 10.1021/Ja505823S  0.447
2014 Wu J, Yang X, He Z, Mao X, Hatton TA, Jamison TF. Continuous flow synthesis of ketones from carbon dioxide and organolithium or Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 8416-20. PMID 24961600 DOI: 10.1002/Anie.201405014  0.443
2014 Standley EA, Smith SJ, Müller P, Jamison TF. A Broadly Applicable Strategy for Entry into Homogeneous Nickel(0) Catalysts from Air-Stable Nickel(II) Complexes. Organometallics. 33: 2012-2018. PMID 24803717 DOI: 10.1021/Om500156Q  0.363
2014 Yang X, Wu J, Mao X, Jamison TF, Hatton TA. Microwave assisted synthesis of cyclic carbonates from olefins with sodium bicarbonates as the C1 source. Chemical Communications (Cambridge, England). 50: 3245-8. PMID 24522755 DOI: 10.1039/C4Cc00252K  0.302
2014 Wu J, Kozak JA, Simeon F, Hatton TA, Jamison TF. Mechanism-guided design of flow systems for multicomponent reactions: Conversion of CO2 and olefins to cyclic carbonates Chemical Science. 5: 1227-1231. DOI: 10.1039/C3Sc53422G  0.446
2014 Zhang P, Russell MG, Jamison TF. Continuous flow total synthesis of rufinamide Organic Process Research and Development. 18: 1567-1570. DOI: 10.1021/Op500166N  0.484
2014 Heider PL, Born SC, Basak S, Benyahia B, Lakerveld R, Zhang H, Hogan R, Buchbinder L, Wolfe A, Mascia S, Evans JMB, Jamison TF, Jensen KF. Development of a multi-step synthesis and workup sequence for an integrated, continuous manufacturing process of a pharmaceutical Organic Process Research and Development. 18: 402-409. DOI: 10.1021/Op400294Z  0.39
2013 Kozak JA, Wu J, Su X, Simeon F, Hatton TA, Jamison TF. Bromine-catalyzed conversion of CO2 and epoxides to cyclic carbonates under continuous flow conditions. Journal of the American Chemical Society. 135: 18497-501. PMID 24256033 DOI: 10.1021/Ja4079094  0.363
2013 Mascia S, Heider PL, Zhang H, Lakerveld R, Benyahia B, Barton PI, Braatz RD, Cooney CL, Evans JM, Jamison TF, Jensen KF, Myerson AS, Trout BL. End-to-end continuous manufacturing of pharmaceuticals: integrated synthesis, purification, and final dosage formation. Angewandte Chemie (International Ed. in English). 52: 12359-63. PMID 24115355 DOI: 10.1002/Anie.201305429  0.337
2013 Byers JA, Jamison TF. Entropic factors provide unusual reactivity and selectivity in epoxide-opening reactions promoted by water. Proceedings of the National Academy of Sciences of the United States of America. 110: 16724-9. PMID 24046369 DOI: 10.1073/Pnas.1311133110  0.61
2013 Schleicher KD, Jamison TF. A reductive coupling strategy towards ripostatin A. Beilstein Journal of Organic Chemistry. 9: 1533-50. PMID 23946853 DOI: 10.3762/Bjoc.9.175  0.378
2013 Mousseau JJ, Morten CJ, Jamison TF. A dioxane template for highly selective epoxy alcohol cyclizations. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10004-16. PMID 23775936 DOI: 10.1002/Chem.201300845  0.427
2013 Zhang Y, Blackman ML, Leduc AB, Jamison TF. Peptide fragment coupling using a continuous-flow photochemical rearrangement of nitrones. Angewandte Chemie (International Ed. in English). 52: 4251-5. PMID 23460372 DOI: 10.1002/Anie.201300504  0.325
2013 Standley EA, Jamison TF. Simplifying nickel(0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes. Journal of the American Chemical Society. 135: 1585-92. PMID 23316879 DOI: 10.1021/Ja3116718  0.457
2012 Shen B, Bedore MW, Sniady A, Jamison TF. Continuous flow photocatalysis enhanced using an aluminum mirror: rapid and selective synthesis of 2'-deoxy and 2',3'-dideoxynucleosides. Chemical Communications (Cambridge, England). 48: 7444-6. PMID 22728875 DOI: 10.1039/C2Cc33356B  0.437
2012 Shen B, Jamison TF. Rapid continuous synthesis of 5'-deoxyribonucleosides in flow via Brønsted acid catalyzed glycosylation. Organic Letters. 14: 3348-51. PMID 22694250 DOI: 10.1021/Ol301324G  0.421
2012 Webb D, Jamison TF. A continuous homologation of esters: an efficient telescoped reduction-olefination sequence. Organic Letters. 14: 2465-7. PMID 22545983 DOI: 10.1021/Ol300722E  0.391
2012 Tucker JW, Zhang Y, Jamison TF, Stephenson CR. Visible-light photoredox catalysis in flow. Angewandte Chemie (International Ed. in English). 51: 4144-7. PMID 22431004 DOI: 10.1002/Anie.201200961  0.714
2012 Gutierrez AC, Jamison TF. Scalable and Robust Synthesis of CpRu(MeCN)3PF6via Continuous Flow Photochemistry Journal of Flow Chemistry. 1: 24-27. DOI: 10.1556/Jfchem.2011.00004  0.433
2012 Nagy KD, Shen B, Jamison TF, Jensen KF. Mixing and dispersion in small-scale flow systems Organic Process Research and Development. 16: 976-981. DOI: 10.1021/Op200349F  0.404
2012 Yu J, Meijer EW, Booker SJ, Mapp AK, Jamison TF, Aube J, Wasielewski MR, Schuster DI, Snyder SA, Tang Y, Chang CJ, Glorius F, Feringa B. Arthur C. Cope Scholar Awards and Eli Lilly Award Angewandte Chemie. 51: 8693-8694. DOI: 10.1002/Anie.201204828  0.563
2011 Gutierrez AC, Jamison TF. Continuous photochemical generation of catalytically active [CpRu]+ complexes from CpRu(η6-C6H6)PF6. Organic Letters. 13: 6414-7. PMID 22085085 DOI: 10.1021/Ol2027015  0.459
2011 Matsubara R, Gutierrez AC, Jamison TF. Nickel-catalyzed Heck-type reactions of benzyl chlorides and simple olefins. Journal of the American Chemical Society. 133: 19020-3. PMID 22066899 DOI: 10.1021/Ja209235D  0.473
2011 Beaver MG, Jamison TF. Ni(II) salts and 2-propanol effect catalytic reductive coupling of epoxides and alkynes. Organic Letters. 13: 4140-3. PMID 21718038 DOI: 10.1021/Ol201702A  0.309
2011 Matsubara R, Jamison TF. Nickel-catalyzed allylic substitution of simple alkenes. Chemistry, An Asian Journal. 6: 1860-75. PMID 21387565 DOI: 10.1002/Asia.201000875  0.473
2011 Sniady A, Bedore MW, Jamison TF. One-flow, multistep synthesis of nucleosides by Brønsted acid-catalyzed glycosylation. Angewandte Chemie (International Ed. in English). 50: 2155-8. PMID 21344574 DOI: 10.1002/Anie.201006440  0.406
2011 Morten CJ, Byers JA, Jamison TF. Evidence that epoxide-opening cascades promoted by water are stepwise and become faster and more selective after the first cyclization. Journal of the American Chemical Society. 133: 1902-8. PMID 21235230 DOI: 10.1021/Ja1088748  0.65
2011 Zhang Y, Jamison TF, Patel S, Mainolfi N. Continuous flow coupling and decarboxylation reactions promoted by copper tubing. Organic Letters. 13: 280-3. PMID 21141809 DOI: 10.1021/Ol1026848  0.416
2011 Zaborenko N, Bedore MW, Jamison TF, Jensen KF. Kinetic and scale-up investigations of epoxide aminolysis in microreactors at high temperatures and pressures Organic Process Research and Development. 15: 131-139. DOI: 10.1021/Op100252M  0.4
2010 Matsubara R, Jamison TF. Nickel-catalyzed allylic substitution of simple alkenes. Journal of the American Chemical Society. 132: 6880-1. PMID 20433144 DOI: 10.1021/Ja101186P  0.441
2010 Heffron TP, Simpson GL, Merino E, Jamison TF. Ladder polyether synthesis via epoxide-opening cascades directed by a disappearing trimethylsilyl group. The Journal of Organic Chemistry. 75: 2681-701. PMID 20302314 DOI: 10.1021/Jo1002455  0.384
2010 Kondoh A, Jamison TF. Rhodium-catalyzed dehydrogenative borylation of cyclic alkenes. Chemical Communications (Cambridge, England). 46: 907-9. PMID 20107646 DOI: 10.1055/S-0029-1219667  0.472
2010 Liu P, McCarren P, Cheong PH, Jamison TF, Houk KN. Origins of regioselectivity and alkene-directing effects in nickel-catalyzed reductive couplings of alkynes and aldehydes. Journal of the American Chemical Society. 132: 2050-7. PMID 20095609 DOI: 10.1021/Ja909562Y  0.454
2010 Jensen KF, Bedore MW, Zaborenko N, Jamison TF. Aminolysis of epoxides in a microreactor system: A continuous flow approach to β-Amino alcohols Organic Process Research and Development. 14: 432-440. DOI: 10.1021/Op9003136  0.426
2010 Ho C, Schleicher KD, Chan C, Jamison TF. ChemInform Abstract: Catalytic Addition of Simple Alkenes to Carbonyl Compounds by Use of Group 10 Metals Cheminform. 41. DOI: 10.1002/CHIN.201002259  0.623
2009 Ho CY, Schleicher KD, Jamison TF. Catalytic Addition of Simple Alkenes to Carbonyl Compounds Using Group 10 Metals. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2009: 2565-2582. PMID 21904421 DOI: 10.1055/S-0029-1217747  0.713
2009 Sparling BA, Simpson GL, Jamison TF. Strategic use of nickel(0)-catalyzed enyne-epoxide reductive coupling towards the synthesis of (-)-cyatha-3,12-diene. Tetrahedron. 65: 3270-3280. PMID 20161213 DOI: 10.1016/J.Tet.2008.11.086  0.463
2009 Morten CJ, Byers JA, Van Dyke AR, Vilotijevic I, Jamison TF. The development of endo-selective epoxide-opening cascades in water. Chemical Society Reviews. 38: 3175-92. PMID 19847350 DOI: 10.1039/B816697H  0.781
2009 Van Dyke AR, Jamison TF. Functionalized templates for the convergent assembly of polyethers: synthesis of the HIJK rings of gymnocin A. Angewandte Chemie (International Ed. in English). 48: 4430-2. PMID 19431181 DOI: 10.1002/Anie.200900924  0.786
2009 McCarren PR, Liu P, Cheong PH, Jamison TF, Houk KN. Mechanism and transition-state structures for nickel-catalyzed reductive alkyne-aldehyde coupling reactions. Journal of the American Chemical Society. 131: 6654-5. PMID 19397371 DOI: 10.1021/Ja900701G  0.376
2009 Byers JA, Jamison TF. On the synergism between H2O and a tetrahydropyran template in the regioselective cyclization of an epoxy alcohol. Journal of the American Chemical Society. 131: 6383-5. PMID 19385615 DOI: 10.1021/Ja9004909  0.559
2008 Ng SS, Ho CY, Schleicher KD, Jamison TF. Nickel-Catalyzed Coupling Reactions of Alkenes. Pure and Applied Chemistry. Chimie Pure Et Appliquee. 80: 929-939. PMID 21814295 DOI: 10.1351/Pac200880050929  0.724
2008 Ho CY, Ohmiya H, Jamison TF. Alpha-olefins as alkenylmetal equivalents in catalytic conjugate addition reactions. Angewandte Chemie (International Ed. in English). 47: 1893-5. PMID 18236501 DOI: 10.1002/Anie.200705163  0.795
2008 Ho C, Ohmiya H, Jamison TF. ChemInform Abstract: α-Olefins as Alkenylmetal Equivalents in Catalytic Conjugate Addition Reactions. Cheminform. 39. DOI: 10.1002/CHIN.200828075  0.667
2007 Moslin RM, Jamison TF. Total synthesis of (+)-acutiphycin. The Journal of Organic Chemistry. 72: 9736-45. PMID 17985925 DOI: 10.1021/Jo701821H  0.501
2007 Moslin RM, Miller-Moslin K, Jamison TF. Regioselectivity and enantioselectivity in nickel-catalysed reductive coupling reactions of alkynes. Chemical Communications (Cambridge, England). 4441-9. PMID 17971951 DOI: 10.1039/B707737H  0.453
2007 Woodin KS, Jamison TF. Total synthesis of pumiliotoxins 209F and 251D via late-stage, nickel-catalyzed epoxide-alkyne reductive cyclization. The Journal of Organic Chemistry. 72: 7451-4. PMID 17696401 DOI: 10.1021/Jo071132E  0.418
2007 Ho CY, Jamison TF. Highly selective coupling of alkenes and aldehydes catalyzed by [Ni(NHC){P(OPh)3}]: synergy between a strong sigma donor and a strong pi acceptor. Angewandte Chemie (International Ed. in English). 46: 782-5. PMID 17154217 DOI: 10.1002/Anie.200603907  0.696
2007 Van Dyke AR, Miller KM, Jamison TF. (S)-(+)-neomenthyldiphenylphosphine in nickel-catalyzed asymmetric reductive coupling of alkynes and aldehydes: Enantioselective synthesis of allylic alcohols and α-hydroxy ketones Organic Syntheses. 84: 111-119. DOI: 10.1002/0471264229.Os084.11  0.399
2006 Moslin RM, Jamison TF. Highly convergent total synthesis of (+)-acutiphycin. Journal of the American Chemical Society. 128: 15106-7. PMID 17117859 DOI: 10.1021/Ja0670660  0.458
2006 Ng SS, Ho CY, Jamison TF. Nickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates. Journal of the American Chemical Society. 128: 11513-28. PMID 16939275 DOI: 10.1021/Ja062866W  0.714
2006 Ho CY, Ng SS, Jamison TF. Nickel-catalyzed, carbonyl-ene-type reactions: selective for alpha olefins and more efficient with electron-rich aldehydes. Journal of the American Chemical Society. 128: 5362-3. PMID 16620106 DOI: 10.1021/Ja061471+  0.706
2006 Moslin RM, Jamison TF. Mechanistic implications of nickel-catalyzed reductive coupling of aldehydes and chiral 1,6-enynes. Organic Letters. 8: 455-8. PMID 16435858 DOI: 10.1021/Ol052719N  0.459
2006 Simpson GL, Heffron TP, Merino E, Jamison TF. Ladder polyether synthesis via epoxide-opening cascades using a disappearing directing group. Journal of the American Chemical Society. 128: 1056-7. PMID 16433504 DOI: 10.1021/Ja057973P  0.356
2006 Ng SS, Jamison TF. Nickel-catalyzed coupling of terminal allenes, aldehydes, and silanes Tetrahedron. 62: 11350-11359. DOI: 10.1016/J.Tet.2006.05.006  0.432
2006 Moslin RM, Miller KM, Jamison TF. Directing effects of tethered alkenes in nickel-catalyzed coupling reactions of 1,6-enynes and aldehydes Tetrahedron. 62: 7598-7610. DOI: 10.1016/J.Tet.2006.03.122  0.472
2005 Miller KM, Jamison TF. Highly regioselective, catalytic asymmetric reductive coupling of 1,3-enynes and ketones. Organic Letters. 7: 3077-80. PMID 15987209 DOI: 10.1021/Ol051075G  0.452
2005 Colby EA, O'Brien KC, Jamison TF. Total syntheses of amphidinolides T1 and T4 via catalytic, stereoselective, reductive macrocyclizations. Journal of the American Chemical Society. 127: 4297-307. PMID 15783211 DOI: 10.1021/Ja042733F  0.426
2005 O'Brien KC, Colby EA, Jamison TF. Synthesis of C13-C22 of amphidinolide T2 via nickel-catalyzed reductive coupling of an alkyne and a terminal epoxide Tetrahedron. 61: 6243-6248. DOI: 10.1016/J.Tet.2005.03.116  0.416
2005 Miller KM, Colby EA, Woodin KS, Jamison TF. Asymmetric catalytic reductive coupling of 1,3-enynes and aromatic aldehydes Advanced Synthesis and Catalysis. 347: 1533-1536. DOI: 10.1002/Adsc.200505175  0.472
2004 Molinaro C, Jamison TF. Catalytic reductive coupling of epoxides and aldehydes: epoxide-ring opening precedes carbonyl reduction. Angewandte Chemie (International Ed. in English). 44: 129-32. PMID 15599916 DOI: 10.1002/Anie.200461705  0.653
2004 Miller KM, Jamison TF. Ligand-switchable directing effects of tethered alkenes in nickel-catalyzed additions to alkynes. Journal of the American Chemical Society. 126: 15342-3. PMID 15563136 DOI: 10.1021/Ja0446799  0.455
2004 Chan J, Jamison TF. Enantioselective synthesis of (-)-terpestacin and structural revision of siccanol using catalytic stereoselective fragment couplings and macrocyclizations. Journal of the American Chemical Society. 126: 10682-91. PMID 15327327 DOI: 10.1021/Ja0470968  0.438
2004 Patel SJ, Jamison TF. Asymmetric catalytic coupling of organoboranes, alkynes, and imines with a removable (trialkylsilyloxy)ethyl group--direct access to enantiomerically pure primary allylic amines. Angewandte Chemie (International Ed. in English). 43: 3941-4. PMID 15274220 DOI: 10.1002/Anie.200460044  0.398
2004 Miller KM, Luanphaisarnnont T, Molinaro C, Jamison TF. Alkene-directed, nickel-catalyzed alkyne coupling reactions. Journal of the American Chemical Society. 126: 4130-1. PMID 15053602 DOI: 10.1021/Ja0491735  0.71
2004 Colby EA, O'Brien KC, Jamison TF. Synthesis of amphidinolide T1 via catalytic, stereoselective macrocyclization. Journal of the American Chemical Society. 126: 998-9. PMID 14746449 DOI: 10.1021/Ja039716V  0.429
2003 Molinaro C, Jamison TF. Nickel-catalyzed reductive coupling of alkynes and epoxides. Journal of the American Chemical Society. 125: 8076-7. PMID 12837057 DOI: 10.1021/Ja0361401  0.696
2003 Patel SJ, Jamison TF. Catalytic three-component coupling of alkynes, imines, and organoboron reagents. Angewandte Chemie (International Ed. in English). 42: 1364-7. PMID 12671969 DOI: 10.1002/Anie.200390349  0.362
2003 Miller KM, Molinaro C, Jamison TF. Catalytic reductive carbon-carbon bond-forming reactions of alkynes Tetrahedron Asymmetry. 14: 3619-3625. DOI: 10.1016/J.Tetasy.2003.07.010  0.68
2003 Heffron TP, Trenkle JD, Jamison TF. Synthesis of skipped enynes via phosphine-promoted couplings of propargylcopper reagents Tetrahedron. 59: 8913-8917. DOI: 10.1016/J.Tet.2003.04.002  0.449
2003 Jamison TF, Lubell WD, Dener JM, Krisché MJ, Rapoport H. 9‐Bromo‐9‐Phenylfluorene Organic Syntheses. 220-220. DOI: 10.1002/0471264180.Os071.28  0.553
2002 Skaggs AJ, Lin EY, Jamison TF. Cobalt cluster-containing carbonyl ylides for catalytic, three-component assembly of oxygen heterocycles. Organic Letters. 4: 2277-80. PMID 12074686 DOI: 10.1021/Ol026149S  0.373
2001 Thompson CF, Jamison TF, Jacobsen EN. FR901464: total synthesis, proof of structure, and evaluation of synthetic analogues. Journal of the American Chemical Society. 123: 9974-83. PMID 11592876 DOI: 10.1021/Ja016615T  0.62
2000 Huang WS, Chan J, Jamison TF. Highly selective catalytic intermolecular reductive coupling of alkynes and aldehydes Organic Letters. 2: 4221-3. PMID 11150204 DOI: 10.1021/Ol006781Q  0.44
2000 Thompson CF, Jamison TF, Jacobsen EN. Total synthesis of FR901464. Convergent assembly of chiral components prepared by asymmetric catalysis [17] Journal of the American Chemical Society. 122: 10482-10483. DOI: 10.1021/Ja0055357  0.491
1999 Dossetter AG, Jamison TF, Jacobsen EN. Highly Enantio- and Diastereoselective Hetero-Diels-Alder Reactions Catalyzed by New Chiral Tridentate Chromium(III) Catalysts. Angewandte Chemie (International Ed. in English). 38: 2398-2400. PMID 10458800 DOI: 10.1002/(Sici)1521-3773(19990816)38:16<2398::Aid-Anie2398>3.0.Co;2-E  0.595
1999 Dossetter A, Jamison T, Jacobsen E. Hochenantio- und -diastereoselektive Hetero-Diels-Alder-Reaktionen, katalyisert durch neue chirale Chrom(III)-Komplexe Angewandte Chemie. 111: 2549-2552. DOI: 10.1002/(Sici)1521-3757(19990816)111:16<2549::Aid-Ange2549>3.0.Co;2-H  0.511
1998 Francis MB, Jamison TF, Jacobsen EN. Combinatorial libraries of transition-metal complexes, catalysts and materials. Current Opinion in Chemical Biology. 2: 422-8. PMID 9691076 DOI: 10.1016/S1367-5931(98)80019-7  0.67
1997 Jamison TF, Shambayati S, Crowe WE, Schreiber SL. Tandem use of cobalt-mediated reactions to synthesize (+)- epoxydictymene, a diterpene containing a trans-fused 5-5 ring system Journal of the American Chemical Society. 119: 4353-4363. DOI: 10.1021/Ja970022U  0.576
1996 Hung DT, Jamison TF, Schreiber SL. Understanding and controlling the cell cycle with natural products. Chemistry & Biology. 3: 623-39. PMID 8807895 DOI: 10.1016/S1074-5521(96)90129-5  0.625
1994 Jamison TF, Shambayati S, Crowe WE, Schreiber SL. Cobalt-mediated total synthesis of (+)-epoxydictymene Journal of the American Chemical Society. 116: 5505-5506. DOI: 10.1021/Ja00091A079  0.524
1990 Lubell WD, Jamison TF, Rapoport H. N-(9-phenylfluoren-9-yl)-α-amino ketones and N-(9-phenylfluoren-9-yl)-α-amino aldehydes as chiral educts for the synthesis of optically pure 4-alkyl-3-hydroxy-2-amino acids. Synthesis of the C-9 amino acid MeBmt present in cyclosporin Journal of Organic Chemistry. 55: 3511-3522. DOI: 10.1021/Jo00298A025  0.486
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