| 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 |
0.33 |
|
| 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 |
0.777 |
|
| 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 |
0.821 |
|
| 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 |
|
| 2020 |
Nguyen LV, Jamison TF. Total Synthesis of (±)-Sceptrin. Organic Letters. PMID 32379973 DOI: 10.1021/Acs.Orglett.0C01381 |
0.405 |
|
| 2020 |
Jamison TF, Monos TM, Jaworski JN, Stephens JC. Continuous-Flow Synthesis of Tramadol from Cyclohexanone Synlett. 31: 1888-1893. DOI: 10.1055/S-0039-1690884 |
0.454 |
|
| 2020 |
Breen CP, Parrish C, Shangguan N, Majumdar S, Murnen H, Jamison TF, Bio MM. A Scalable Membrane Pervaporation Approach for Continuous Flow Olefin Metathesis Organic Process Research & Development. 24: 2298-2303. DOI: 10.1021/Acs.Oprd.0C00061 |
0.335 |
|
| 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 |
0.431 |
|
| 2019 |
Mear SJ, Jamison TF. Diazotization of -Sulfonyl-cysteines. The Journal of Organic Chemistry. PMID 31657562 DOI: 10.1021/Acs.Joc.9B02630 |
0.304 |
|
| 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 |
0.44 |
|
| 2019 |
Kelley EH, Jamison TF. Synthesis of the Framework of Tamulamides A and B. Organic Letters. PMID 31523969 DOI: 10.1021/Acs.Orglett.9B03015 |
0.385 |
|
| 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 |
0.398 |
|
| 2019 |
Fu WC, Jamison TF. Modular Continuous Flow Synthesis of Imatinib and Analogues. Organic Letters. PMID 31314541 DOI: 10.1021/Acs.Orglett.9B02259 |
0.785 |
|
| 2019 |
Sittihan S, Jamison TF. Total Synthesis of the Marine Ladder Polyether Gymnocin B. Journal of the American Chemical Society. 141: 11239-11244. PMID 31283211 DOI: 10.1021/Jacs.9B04696 |
0.365 |
|
| 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 |
0.432 |
|
| 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 |
0.459 |
|
| 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 |
0.428 |
|
| 2019 |
Russell MG, Veryser C, Hunter JF, Beingessner RL, Jamison TF. Monolithic Silica Support for Immobilized Catalysis in Continuous Flow Advanced Synthesis & Catalysis. 362: 314-319. DOI: 10.1002/Adsc.201901185 |
0.334 |
|
| 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 |
0.327 |
|
| 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 |
0.386 |
|
| 2018 |
Weber JM, Longstreet AR, Jamison TF. Bench-Stable Nickel Precatalysts with Heck-type Activation. Organometallics. 37: 2716-2722. PMID 30174368 DOI: 10.1021/Acs.Organomet.8B00351 |
0.38 |
|
| 2018 |
Strieth-Kalthoff F, Longstreet AR, Weber JM, Jamison TF. Bench-Stable -Heterocyclic Carbene Nickel Precatalysts for C-C and C-N Bond-Forming Reactions. Chemcatchem. 10: 2873-2877. PMID 30147804 DOI: 10.1002/Cctc.201800454 |
0.384 |
|
| 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 |
0.761 |
|
| 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 |
0.468 |
|
| 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 |
0.398 |
|
| 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 |
0.387 |
|
| 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 |
0.809 |
|
| 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 |
0.447 |
|
| 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 |
0.562 |
|
| 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 |
0.769 |
|
| 2018 |
Seo H, Bédard A, Chen WP, Hicklin RW, Alabugin A, Jamison TF. Selective N-monomethylation of primary anilines with dimethyl carbonate in continuous flow Tetrahedron. 74: 3124-3128. DOI: 10.1016/J.Tet.2017.11.068 |
0.422 |
|
| 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 |
0.306 |
|
| 2018 |
Seo H, Nguyen LV, Jamison TF. Using Carbon Dioxide as a Building Block in Continuous Flow Synthesis Advanced Synthesis & Catalysis. 361: 247-264. DOI: 10.1002/Adsc.201801228 |
0.373 |
|
| 2017 |
Britton J, Jamison TF. The assembly and use of continuous flow systems for chemical synthesis. Nature Protocols. 12: 2423-2446. PMID 29072707 DOI: 10.1038/Nprot.2017.102 |
0.436 |
|
| 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 |
0.323 |
|
| 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 |
0.53 |
|
| 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 |
0.645 |
|
| 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 |
0.49 |
|
| 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 |
0.792 |
|
| 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 |
0.377 |
|
| 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 |
0.472 |
|
| 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 |
0.709 |
|
| 2017 |
Su X, Tan K, Elbert J, Rüttiger C, Gallei M, Jamison TF, Hatton TA. Asymmetric Faradaic systems for selective electrochemical separations Energy & Environmental Science. 10: 1272-1283. DOI: 10.1039/C7Ee00066A |
0.341 |
|
| 2017 |
Britton J, Jamison TF. Synthesis of Celecoxib, Mavacoxib, SC-560, Fluxapyroxad, and Bixafen Enabled by Continuous Flow Reaction Modules European Journal of Organic Chemistry. 2017: 6566-6574. DOI: 10.1002/Ejoc.201700992 |
0.477 |
|
| 2016 |
McTeague TA, Jamison TF. Photoredox Activation of SF6 for Fluorination. Angewandte Chemie (International Ed. in English). PMID 27813242 DOI: 10.1002/Anie.201608792 |
0.432 |
|
| 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 |
0.409 |
|
| 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 |
0.438 |
|
| 2016 |
Andrade LH, Sousa BA, Jamison TF. Confining a biocatalyst for highly efficient and selective synthesis of carboxamide derivatives under continuous-flow conditions Journal of Flow Chemistry. 6: 67-72. DOI: 10.1556/1846.2016.00008 |
0.463 |
|
| 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 |
0.438 |
|
| 2016 |
Su X, Kulik HJ, Jamison TF, Hatton TA. Anion-Selective Redox Electrodes: Electrochemically Mediated Separation with Heterogeneous Organometallic Interfaces Advanced Functional Materials. 26: 3394-3404. DOI: 10.1002/Adfm.201600079 |
0.304 |
|
| 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 |
0.661 |
|
| 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 |
0.713 |
|
| 2015 |
Tasker SZ, Jamison TF. Highly Regioselective Indoline Synthesis under Nickel/Photoredox Dual Catalysis. Journal of the American Chemical Society. 137: 9531-4. PMID 26196355 DOI: 10.1021/Jacs.5B05597 |
0.395 |
|
| 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 |
0.81 |
|
| 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 |
0.511 |
|
| 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 |
0.466 |
|
| 2015 |
Ocampo CE, Lee D, Jamison TF. Selective Lewis acid catalyzed assembly of phosphonomethyl ethers: three-step synthesis of tenofovir. Organic Letters. 17: 820-3. PMID 25664399 DOI: 10.1021/Ol503612H |
0.424 |
|
| 2015 |
Czabaniuk LC, Jamison TF. Hydroxyl-substituted ladder polyethers via selective tandem epoxidation/cyclization sequence. Organic Letters. 17: 774-7. PMID 25647091 DOI: 10.1021/Ol503400J |
0.445 |
|
| 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 |
0.329 |
|
| 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 |
0.406 |
|
| 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 |
0.555 |
|
| 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 |
0.678 |
|
| 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 |
0.471 |
|
| 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 |
0.392 |
|
| 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 |
0.442 |
|
| 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 |
0.466 |
|
| 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 |
0.464 |
|
| 2014 |
Tasker SZ, Standley EA, Jamison TF. Recent advances in homogeneous nickel catalysis. Nature. 509: 299-309. PMID 24828188 DOI: 10.1038/Nature13274 |
0.322 |
|
| 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 |
0.372 |
|
| 2014 |
He Z, Jamison TF. Continuous-flow synthesis of functionalized phenols by aerobic oxidation of Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 3353-7. PMID 24554581 DOI: 10.1002/Anie.201310572 |
0.386 |
|
| 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 |
0.306 |
|
| 2014 |
Tasker SZ, Gutierrez AC, Jamison TF. Nickel-catalyzed Mizoroki-Heck reaction of aryl sulfonates and chlorides with electronically unbiased terminal olefins: high selectivity for branched products. Angewandte Chemie (International Ed. in English). 53: 1858-61. PMID 24402966 DOI: 10.1002/Anie.201308391 |
0.455 |
|
| 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 |
0.463 |
|
| 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 |
0.509 |
|
| 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 |
0.403 |
|
| 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 |
0.373 |
|
| 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 |
0.344 |
|
| 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 |
0.616 |
|
| 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 |
0.39 |
|
| 2013 |
Underwood BS, Tanuwidjaja J, Ng SS, Jamison TF. Total syntheses of the squalene-derived halogenated polyethers ent-dioxepandehydrothyrsiferol and armatol A via bromonium- and Lewis acid-initiated epoxide-opening cascades. Tetrahedron. 69: 5205-5220. PMID 23878408 DOI: 10.1016/J.Tet.2013.04.041 |
0.433 |
|
| 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 |
0.449 |
|
| 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 |
0.328 |
|
| 2013 |
Kleinke AS, Jamison TF. Hydrogen-free alkene reduction in continuous flow. Organic Letters. 15: 710-3. PMID 23339476 DOI: 10.1021/Ol400051N |
0.331 |
|
| 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 |
0.481 |
|
| 2013 |
Shen B, Jamison TF. Continuous flow photochemistry for the rapid and selective synthesis of 2′-deoxy and 2′,3′-dideoxynucleosides Australian Journal of Chemistry. 66: 157-164. DOI: 10.1071/Ch12426 |
0.491 |
|
| 2013 |
Snead DR, Jamison TF. End-to-end continuous flow synthesis and purification of diphenhydramine hydrochloride featuring atom economy, in-line separation, and flow of molten ammonium salts Chemical Science. 4: 2822-2827. DOI: 10.1039/C3Sc50859E |
0.372 |
|
| 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 |
0.454 |
|
| 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 |
0.44 |
|
| 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 |
0.408 |
|
| 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 |
0.725 |
|
| 2012 |
Webb D, Jamison TF. Diisobutylaluminum hydride reductions revitalized: a fast, robust, and selective continuous flow system for aldehyde synthesis. Organic Letters. 14: 568-71. PMID 22206502 DOI: 10.1021/Ol2031872 |
0.406 |
|
| 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 |
0.45 |
|
| 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 |
0.414 |
|
| 2012 |
Leduc AB, Jamison TF. Continuous flow oxidation of alcohols and aldehydes utilizing bleach and catalytic tetrabutylammonium bromide Organic Process Research and Development. 16: 1082-1089. DOI: 10.1021/Op200118H |
0.312 |
|
| 2012 |
Kleinke AS, Webb D, Jamison TF. Recent progress in the synthesis of oxepanes and medium ring ethers Tetrahedron. 68: 6999-7018. DOI: 10.1016/J.Tet.2012.05.081 |
0.383 |
|
| 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 |
0.552 |
|
| 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 |
0.477 |
|
| 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 |
0.497 |
|
| 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 |
0.316 |
|
| 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 |
0.498 |
|
| 2011 |
Palde PB, Jamison TF. Safe and efficient tetrazole synthesis in a continuous-flow microreactor. Angewandte Chemie (International Ed. in English). 50: 3525-8. PMID 21387506 DOI: 10.1002/Anie.201006272 |
0.422 |
|
| 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 |
0.423 |
|
| 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 |
0.663 |
|
| 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 |
0.43 |
|
| 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 |
0.414 |
|
| 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 |
0.463 |
|
| 2010 |
Vilotijevic I, Jamison TF. Synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascades. Marine Drugs. 8: 763-809. PMID 20411125 DOI: 10.3390/Md8030763 |
0.44 |
|
| 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 |
0.399 |
|
| 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 |
0.496 |
|
| 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 |
0.473 |
|
| 2010 |
Tanuwidjaja J, Ng S-, Jamison TF. Synthesis of ent-Dioxepandehydrothyrsiferol Synfacts. 2010: 137-137. DOI: 10.1055/S-0029-1219026 |
0.417 |
|
| 2010 |
Trenkle JD, Jamison TF. Synthesis of Gloeosporone Synfacts. 2010: 7-7. DOI: 10.1055/S-0029-1218263 |
0.417 |
|
| 2010 |
Webb D, Jamison TF. Continuous flow multi-step organic synthesis Chemical Science. 1: 675-680. DOI: 10.1039/C0Sc00381F |
0.42 |
|
| 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 |
0.442 |
|
| 2010 |
Foley MA, Jamison TF. Amide bond formation via reversible, carboxylic acid-promoted lactone aminolysis Organic Process Research and Development. 14: 1177-1181. DOI: 10.1021/Op1001269 |
0.328 |
|
| 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 |
0.619 |
|
| 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 |
0.718 |
|
| 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 |
0.489 |
|
| 2009 |
Morten CJ, Jamison TF. New synthetic strategies for the stereocontrolled synthesis of substituted "skipped" diepoxides. Tetrahedron. 65: 6648-6655. PMID 20161178 DOI: 10.1016/J.Tet.2009.05.074 |
0.413 |
|
| 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 |
0.785 |
|
| 2009 |
Tanuwidjaja J, Ng SS, Jamison TF. Total synthesis of ent-dioxepandehydrothyrsiferol via a bromonium-initiated epoxide-opening cascade. Journal of the American Chemical Society. 131: 12084-5. PMID 19663441 DOI: 10.1021/Ja9052366 |
0.42 |
|
| 2009 |
Vilotijevic I, Jamison TF. Epoxide-opening cascades in the synthesis of polycyclic polyether natural products. Angewandte Chemie (International Ed. in English). 48: 5250-81. PMID 19572302 DOI: 10.1002/Anie.200900600 |
0.404 |
|
| 2009 |
Trenkle JD, Jamison TF. Macrocyclization by nickel-catalyzed, ester-promoted, epoxide-alkyne reductive coupling: total synthesis of (-)-gloeosporone. Angewandte Chemie (International Ed. in English). 48: 5366-8. PMID 19536804 DOI: 10.1002/Anie.200902079 |
0.45 |
|
| 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 |
0.793 |
|
| 2009 |
Morten CJ, Jamison TF. Water overcomes methyl group directing effects in epoxide-opening cascades. Journal of the American Chemical Society. 131: 6678-9. PMID 19402635 DOI: 10.1021/Ja9025243 |
0.304 |
|
| 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 |
0.39 |
|
| 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 |
0.561 |
|
| 2009 |
Van Dyke A, Jamison T. Funktionalisierte Template für den konvergenten Aufbau von Polyethern: Synthese der HIJK-Ringe von Gymnocin A Angewandte Chemie. 121: 4494-4496. DOI: 10.1002/Ange.200900924 |
0.3 |
|
| 2009 |
Vilotijevic I, Jamison T. Epoxidöffnungskaskaden zur Synthese polycyclischer Polyether-Naturstoffe Angewandte Chemie. 121: 5352-5385. DOI: 10.1002/Ange.200900600 |
0.34 |
|
| 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 |
0.731 |
|
| 2008 |
Sparling BA, Moslin RM, Jamison TF. SmI2-promoted Reformatsky-type coupling reactions in exceptionally hindered contexts. Organic Letters. 10: 1291-4. PMID 18302397 DOI: 10.1021/Ol800099A |
0.404 |
|
| 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 |
0.802 |
|
| 2008 |
Sparling BA, Moslin RM, Jamison TF. Synthesis of Highly Hindered β-Hydroxy Ketones and E-Enones Synfacts. 2008: 621-621. DOI: 10.1055/S-2008-1078399 |
0.324 |
|
| 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 |
0.668 |
|
| 2007 |
Moslin RM, Jamison TF. Total synthesis of (+)-acutiphycin. The Journal of Organic Chemistry. 72: 9736-45. PMID 17985925 DOI: 10.1021/Jo701821H |
0.528 |
|
| 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 |
0.471 |
|
| 2007 |
Vilotijevic I, Jamison TF. Epoxide-opening cascades promoted by water. Science (New York, N.Y.). 317: 1189-92. PMID 17761875 DOI: 10.1126/Science.1146421 |
0.393 |
|
| 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 |
0.439 |
|
| 2007 |
Schleicher KD, Jamison TF. Nickel-catalyzed synthesis of acrylamides from alpha-olefins and isocyanates. Organic Letters. 9: 875-8. PMID 17269783 DOI: 10.1021/Ol063111X |
0.382 |
|
| 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 |
0.7 |
|
| 2007 |
Jamison T, Moslin R. Synthesis of (+)-Acutiphycin Synfacts. 2007: 0347-0347. DOI: 10.1055/S-2007-968281 |
0.417 |
|
| 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 |
0.419 |
|
| 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 |
0.482 |
|
| 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 |
0.72 |
|
| 2006 |
Langille NF, Jamison TF. trans-hydroalumination/alkylation: one-pot synthesis of trisubstituted allylic alcohols. Organic Letters. 8: 3761-4. PMID 16898811 DOI: 10.1021/Ol0613721 |
0.367 |
|
| 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+ |
0.712 |
|
| 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 |
0.481 |
|
| 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 |
0.37 |
|
| 2006 |
Heffron TP, Jamison TF. Concerning Lewis acid promoted, directing-group-free epoxide-ring-opening cascades Synlett. 2329-2333. DOI: 10.1055/S-2006-949637 |
0.316 |
|
| 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 |
0.454 |
|
| 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 |
0.495 |
|
| 2005 |
Ng SS, Jamison TF. Simple alkenes as substitutes for organometallic reagents: nickel-catalyzed, intermolecular coupling of aldehydes, silyl triflates, and alpha olefins. Journal of the American Chemical Society. 127: 14194-5. PMID 16218608 DOI: 10.1021/Ja055363J |
0.425 |
|
| 2005 |
Colby EA, Jamison TF. A comparative analysis of the total syntheses of the amphidinolide T natural products. Organic & Biomolecular Chemistry. 3: 2675-84. PMID 16032344 DOI: 10.1039/B507315B |
0.323 |
|
| 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 |
0.472 |
|
| 2005 |
Luanphaisarnnont T, Ndubaku CO, Jamison TF. anti-1,2-Diols via Ni-catalyzed reductive coupling of alkynes and alpha-oxyaldehydes. Organic Letters. 7: 2937-40. PMID 15987174 DOI: 10.1021/Ol050881K |
0.43 |
|
| 2005 |
Ng SS, Jamison TF. Highly enantioselective and regioselective nickel-catalyzed coupling of allenes, aldehydes, and silanes. Journal of the American Chemical Society. 127: 7320-1. PMID 15898774 DOI: 10.1021/Ja0521831 |
0.456 |
|
| 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 |
0.446 |
|
| 2005 |
Ng SS, Jamison TF. Enantioselective and regioselective nickel-catalyzed multicomponent coupling of chiral allenes, aromatic aldehydes, and silanes Tetrahedron. 61: 11405-11417. DOI: 10.1016/J.Tet.2005.08.063 |
0.439 |
|
| 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 |
0.436 |
|
| 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 |
0.496 |
|
| 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 |
0.662 |
|
| 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 |
0.478 |
|
| 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 |
0.46 |
|
| 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 |
0.415 |
|
| 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 |
0.723 |
|
| 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 |
0.45 |
|
| 2003 |
Chan J, Jamison TF. Synthesis of (-)-terpestacin via catalytic, stereoselective fragment coupling: siccanol is terpestacin, not 11-epi-terpestacin. Journal of the American Chemical Society. 125: 11514-5. PMID 13129351 DOI: 10.1021/Ja0373925 |
0.417 |
|
| 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 |
0.708 |
|
| 2003 |
Heffron TP, Jamison TF. SiMe3-based homologation-epoxidation-cyclization strategy for ladder THP synthesis. Organic Letters. 5: 2339-42. PMID 12816443 DOI: 10.1021/Ol0347040 |
0.462 |
|
| 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 |
0.373 |
|
| 2003 |
Miller KM, Huang WS, Jamison TF. Catalytic asymmetric reductive coupling of alkynes and aldehydes: enantioselective synthesis of allylic alcohols and alpha-hydroxy ketones. Journal of the American Chemical Society. 125: 3442-3. PMID 12643701 DOI: 10.1021/Ja034366Y |
0.434 |
|
| 2003 |
Colby EA, Jamison TF. P-chiral, monodentate ferrocenyl phosphines, novel ligands for asymmetric catalysis. The Journal of Organic Chemistry. 68: 156-66. PMID 12515474 DOI: 10.1021/Jo0264123 |
0.392 |
|
| 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 |
0.69 |
|
| 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 |
0.472 |
|
| 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 |
0.56 |
|
| 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 |
0.386 |
|
| 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 |
0.636 |
|
| 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 |
0.462 |
|
| 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 |
0.499 |
|
| 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 |
0.605 |
|
| 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 |
0.513 |
|
| 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 |
0.669 |
|
| 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 |
0.591 |
|
| 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 |
0.612 |
|
| 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 |
0.537 |
|
| 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 |
0.493 |
|
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