Year |
Citation |
Score |
2022 |
Hoskin JF, Sorensen EJ. A Concise Synthesis of Pleurotin Enabled by a Nontraditional C-H Epimerization. Journal of the American Chemical Society. 144: 14042-14046. PMID 35900919 DOI: 10.1021/jacs.2c06504 |
0.815 |
|
2021 |
Falcone NA, Bosse AT, Park H, Yu JQ, Davies HML, Sorensen EJ. A C-H Functionalization Strategy Enables an Enantioselective Formal Synthesis of (-)-Aflatoxin B. Organic Letters. PMID 34865494 DOI: 10.1021/acs.orglett.1c03502 |
0.334 |
|
2021 |
Provencher PA, Hoskin JF, Wong JJ, Chen X, Yu JQ, Houk KN, Sorensen EJ. Pd(II)-Catalyzed Synthesis of Benzocyclobutenes by β-Methylene-Selective C(sp)-H Arylation with a Transient Directing Group. Journal of the American Chemical Society. PMID 34817163 DOI: 10.1021/jacs.1c09368 |
0.785 |
|
2020 |
Abrams DJ, Davies HML, Sorensen EJ. Donor-Acceptor-Acceptor 1,3-Bisdiazo Compounds: An Exploration of Synthesis and Stepwise Reactivity. Organic Letters. 22: 1791-1795. PMID 32105078 DOI: 10.1021/Acs.Orglett.0C00103 |
0.33 |
|
2019 |
Reber KP, Gilbert IW, Strassfeld DA, Sorensen EJ. Synthesis of (+)-Lineariifolianone and Related Cyclopropenone-Containing Sesquiterpenoids. The Journal of Organic Chemistry. PMID 30938526 DOI: 10.1021/Acs.Joc.9B00478 |
0.808 |
|
2019 |
Balaguer FA, Mühlethaler T, Estévez-Gallego J, Calvo E, Giménez-Abián JF, Risinger AL, Sorensen EJ, Vanderwal CD, Altmann KH, Mooberry SL, Steinmetz MO, Oliva MÁ, Prota AE, Díaz JF. Crystal Structure of the Cyclostreptin-Tubulin Adduct: Implications for Tubulin Activation by Taxane-Site Ligands. International Journal of Molecular Sciences. 20. PMID 30897704 DOI: 10.3390/Ijms20061392 |
0.566 |
|
2018 |
Chen XY, Sorensen EJ. Ir(iii)-catalyzed C-H alkylations of (hetero)aromatic aldehydes using alkyl boron reagents. Chemical Science. 9: 8951-8956. PMID 30647887 DOI: 10.1039/C8Sc03606C |
0.673 |
|
2018 |
Abrams DJ, Provencher PA, Sorensen EJ. Recent applications of C-H functionalization in complex natural product synthesis. Chemical Society Reviews. PMID 30426998 DOI: 10.1039/C8Cs00716K |
0.378 |
|
2018 |
Forneris CC, Ozturk S, Sorensen EJ, Seyedsayamdost MR. Installation of Multiple Aryl Ether Crosslinks onto Non-Native Substrate Peptides by the Vancomycin OxyB. Tetrahedron. 74: 3231-3237. PMID 30386000 DOI: 10.1016/J.Tet.2018.04.028 |
0.325 |
|
2018 |
Ozturk S, Forneris CC, Nguy AKL, Sorensen EJ, Seyedsayamdost MR. Modulating OxyB-Catalyzed Cross-Coupling Reactions in Vancomycin Biosynthesis by Incorporation of Diverse D-Tyr Analogs. The Journal of Organic Chemistry. PMID 29806454 DOI: 10.1021/Acs.Joc.8B00916 |
0.368 |
|
2018 |
Chen XY, Sorensen EJ. Pd-catalyzed, ortho C-H Methylation and Fluorination of Benzaldehydes Using Orthanilic Acids as Transient Directing Groups. Journal of the American Chemical Society. PMID 29412651 DOI: 10.1021/Jacs.8B00048 |
0.625 |
|
2018 |
Mack JBC, Bedell TA, DeLuca RJ, Hone GAB, Roizen JL, Cox CT, Sorensen EJ, Du Bois J. Rhodium-Catalyzed C–H Amination: A Case Study of Selectivity in C–H Functionalization Reactions Journal of Chemical Education. 95: 2243-2248. DOI: 10.1021/Acs.Jchemed.7B00697 |
0.805 |
|
2017 |
Chen XY, Ozturk S, Sorensen EJ. Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group. Organic Letters. PMID 29129077 DOI: 10.1021/Acs.Orglett.7B02906 |
0.61 |
|
2017 |
Danielsson J, Sun DX, Chen XY, Risinger AL, Mooberry SL, Sorensen EJ. A Stereocontrolled Annulation of the Taccalonolide Epoxy Lactone onto the Molecular Framework of trans-Androsterone. Organic Letters. PMID 28849658 DOI: 10.1021/Acs.Orglett.7B02349 |
0.703 |
|
2017 |
Forneris CC, Ozturk S, Gibson MI, Sorensen EJ, Seyedsayamdost MR. In Vitro Reconstitution of OxyA Enzymatic Activity Clarifies Late Steps in Vancomycin Biosynthesis. Acs Chemical Biology. PMID 28696669 DOI: 10.1021/Acschembio.7B00456 |
0.388 |
|
2017 |
Abrams DJ, West JG, Sorensen EJ. Toward a mild dehydroformylation using base-metal catalysis. Chemical Science. 8: 1954-1959. PMID 28451310 DOI: 10.1039/C6Sc04607J |
0.644 |
|
2017 |
Chen XY, Ozturk S, Sorensen EJ. Synthesis of Fluorenones from Benzaldehydes and Aryl Iodides: Dual C-H Functionalizations Using a Transient Directing Group. Organic Letters. PMID 28225629 DOI: 10.1021/Acs.Orglett.7B00161 |
0.693 |
|
2017 |
West JG, Sorensen EJ. Development of a Bio-Inspired Dual Catalytic System for Alkane Dehydrogenation Israel Journal of Chemistry. 57: 259-269. DOI: 10.1002/Ijch.201600115 |
0.701 |
|
2016 |
Liu J, Marsini MA, Bedell TA, Reider PJ, Sorensen EJ. Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions. Tetrahedron. 72: 3713-3717. PMID 27642195 DOI: 10.1016/J.Tet.2016.03.039 |
0.8 |
|
2016 |
West JG, Bedell TA, Sorensen EJ. The Uranyl Cation as a Visible-Light Photocatalyst for C(sp(3) )-H Fluorination. Angewandte Chemie (International Ed. in English). PMID 27320442 DOI: 10.1002/Anie.201603149 |
0.779 |
|
2016 |
Liu J, Bedell TA, West JG, Sorensen EJ. Design and Synthesis of Molecular Scaffolds with Anti-infective Activity. Tetrahedron. 72: 3579-3592. PMID 27284210 DOI: 10.1016/J.Tet.2016.01.044 |
0.799 |
|
2016 |
Bedell TA, Hone GA, Valette D, Yu JQ, Davies HM, Sorensen EJ. Rapid Construction of a Benzo-Fused Indoxamycin Core Enabled by Site-Selective C-H Functionalizations. Angewandte Chemie (International Ed. in English). 55: 8270-4. PMID 27206223 DOI: 10.1002/Anie.201602024 |
0.828 |
|
2015 |
West JG, Huang D, Sorensen EJ. Acceptorless dehydrogenation of small molecules through cooperative base metal catalysis. Nature Communications. 6: 10093. PMID 26656087 DOI: 10.1038/Ncomms10093 |
0.644 |
|
2015 |
Bedell TA, Hone GA, Bois JD, Sorensen EJ. An expedient synthesis of maraviroc (UK-427,857) via C-H functionalization. Tetrahedron Letters. 56: 3620-3623. PMID 26120216 DOI: 10.1016/J.Tetlet.2015.01.074 |
0.808 |
|
2015 |
Norris MD, Perkins MV, Sorensen EJ. Biomimetic total synthesis of gracilioethers B and C. Organic Letters. 17: 668-71. PMID 25621375 DOI: 10.1021/Ol503695J |
0.35 |
|
2015 |
Liu J, Bedell TA, West JG, Sorensen EJ. Design and synthesis of molecular scaffolds with anti-infective activity Tetrahedron. DOI: 10.1016/j.tet.2016.01.044 |
0.774 |
|
2014 |
Choi J, Park H, Yoo HJ, Kim S, Sorensen EJ, Lee C. Tandem Diels-Alder and retro-ene reactions of 1-sulfenyl- and 1-sulfonyl-1,3-dienes as a traceless route to cyclohexenes. Journal of the American Chemical Society. 136: 9918-21. PMID 24964017 DOI: 10.1021/Ja505721V |
0.448 |
|
2014 |
Siler DA, Mighion JD, Sorensen EJ. An enantiospecific synthesis of jiadifenolide Angewandte Chemie - International Edition. 53: 5332-5335. PMID 24757120 DOI: 10.1002/Anie.201402335 |
0.807 |
|
2013 |
Reber KP, Tilley SD, Carson CA, Sorensen EJ. Toward a synthesis of hirsutellone B by the concept of double cyclization Journal of Organic Chemistry. 78: 9584-9607. PMID 24032341 DOI: 10.1021/Jo401799F |
0.823 |
|
2013 |
Montiel D, Yates EV, Sun L, Sampias MM, Malona J, Sorensen EJ, Yang H. Ligand synthesis and passivation for silver and large gold nanoparticles for single-particle-based sensing and spectroscopy. Methods in Molecular Biology (Clifton, N.J.). 1025: 237-50. PMID 23918342 DOI: 10.1007/978-1-62703-462-3_18 |
0.766 |
|
2013 |
Sorensen EJ, Siler DA, Mighion JD. Taking risks in complex synthesis design Strategies and Tactics in Organic Synthesis. 9: 249-273. DOI: 10.1016/B978-0-08-099362-1.00009-6 |
0.769 |
|
2013 |
Montiel D, Yates EV, Sun L, Sampias MM, Malona J, Sorensen EJ, Yang H. Ligand synthesis and passivation for silver and large gold nanoparticles for single-particle-based sensing and spectroscopy Methods in Molecular Biology. 1025: 237-250. DOI: 10.1007/978-1-62703-462-3_18 |
0.771 |
|
2012 |
Kim J, Schneekloth JS, Sorensen EJ. A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction. Chemical Science (Royal Society of Chemistry : 2010). 3: 2849-2852. PMID 23878716 DOI: 10.1039/C2Sc20669B |
0.65 |
|
2012 |
Sorensen EJ. Organic synthesis: A biochemical messenger made easily Nature. 489: 214-215. PMID 22972292 DOI: 10.1038/489214A |
0.403 |
|
2012 |
Kim J, Schneekloth JS, Sorensen EJ. A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction Chemical Science. 3: 2849-2852. DOI: 10.1039/c2sc20669b |
0.575 |
|
2011 |
Xie H, Sammis GM, Flamme EM, Kraml CM, Sorensen EJ. The catalytic asymmetric Diels-Alder reactions and post-cycloaddition reductive transpositions of 1-hydrazinodienes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 11131-4. PMID 21898626 DOI: 10.1002/Chem.201102394 |
0.822 |
|
2011 |
Guerrero CA, Sorensen EJ. Concise, stereocontrolled synthesis of the citrinadin B core architecture. Organic Letters. 13: 5164-7. PMID 21894952 DOI: 10.1021/Ol2020362 |
0.655 |
|
2011 |
Lotesta SD, Liu J, Yates EV, Krieger I, Sacchettini JC, Freundlich JS, Sorensen EJ. Expanding the pleuromutilin class of antibiotics by de novo chemical synthesis. Chemical Science (Royal Society of Chemistry : 2010). 2: 1258-1261. PMID 21874155 DOI: 10.1039/C1Sc00116G |
0.705 |
|
2011 |
Liu J, Lotesta SD, Sorensen EJ. A concise synthesis of the molecular framework of pleuromutilin Chemical Communications. 47: 1500-1502. PMID 21079876 DOI: 10.1039/C0Cc04077K |
0.667 |
|
2011 |
Lotesta SD, Liu J, Yates EV, Krieger I, Sacchettini JC, Freundlich JS, Sorensen EJ. Expanding the pleuromutilin class of antibiotics by de novo chemical synthesis Chemical Science. 2: 1258-1261. DOI: 10.1039/c1sc00116g |
0.606 |
|
2010 |
Spangler JE, Carson CA, Sorensen EJ. Synthesis enables a structural revision of the Mycobacterium tuberculosis-produced diterpene, edaxadiene. Chemical Science (Royal Society of Chemistry : 2010). 1: 202-205. PMID 22114734 DOI: 10.1039/C0Sc00284D |
0.434 |
|
2010 |
Marsini MA, Reider PJ, Sorensen EJ. A concise and convergent synthesis of PA-824 Journal of Organic Chemistry. 75: 7479-7482. PMID 20929201 DOI: 10.1021/Jo1015807 |
0.779 |
|
2010 |
Freundlich JS, Lalgondar M, Wei JR, Swanson S, Sorensen EJ, Rubin EJ, Sacchettini JC. The abyssomicin C family as in vitro inhibitors of Mycobacterium tuberculosis. Tuberculosis (Edinburgh, Scotland). 90: 298-300. PMID 20739223 DOI: 10.1016/J.Tube.2010.08.002 |
0.306 |
|
2010 |
Chandler BD, Roland JT, Li Y, Sorensen EJ. Seebach's conjunctive reagent enables double cyclizations Organic Letters. 12: 2746-2749. PMID 20481611 DOI: 10.1021/Ol100845Z |
0.787 |
|
2010 |
Reider P, Sorensen E, Marsini M. Synthesis of PA-824 Synfacts. 2011: 0001-0001. DOI: 10.1055/S-0030-1258978 |
0.777 |
|
2010 |
NICOLAOU KC, YANG Z, LIU JJ, UENO H, NANTERMET PG, GUY RK, CLAIBORNE CF, RENAUD J, COULADOUROS EA, PAULVANNAN K, SORENSEN EJ. ChemInform Abstract: Total synthesis of taxol. Cheminform. 25: no-no. DOI: 10.1002/chin.199426230 |
0.644 |
|
2009 |
Schneekloth JS, Kim J, Sorensen EJ. An interrupted Ugi reaction enables the preparation of substituted indoxyls and aminoindoles. Tetrahedron. 65: 3096-3101. PMID 22163373 DOI: 10.1016/J.Tet.2008.08.055 |
0.596 |
|
2009 |
Spangler JE, Sorensen EJ. A Nature-Inspired Diels-Alder Reaction Facilitates Construction of the Bicyclo[2.2.2]octane Core of Andibenin B. Tetrahedron. 65: 6739-6745. PMID 21687810 DOI: 10.1016/J.Tet.2009.06.063 |
0.444 |
|
2009 |
Frie JL, Jeffrey CS, Sorensen EJ. A hypervalent iodine-induced double annulation enables a concise synthesis of the pentacyclic core structure of the cortistatins. Organic Letters. 11: 5394-7. PMID 19943697 DOI: 10.1021/Ol902168G |
0.836 |
|
2009 |
Reber KP, Tilley SD, Sorensen EJ. Bond formations by intermolecular and intramolecular trappings of acylketenes and their applications in natural product synthesis Chemical Society Reviews. 38: 3022-3034. PMID 19847338 DOI: 10.1039/B912599J |
0.825 |
|
2009 |
Tilley SD, Reber KP, Sorensen EJ. A rapid, asymmetric synthesis of the decahydrofluorene core of the hirsutellones Organic Letters. 11: 701-703. PMID 19119873 DOI: 10.1021/Ol802768P |
0.819 |
|
2009 |
Schneekloth JS, Kim J, Sorensen EJ. Preparation of Substituted Indoxyls and Aminoindoles Synfacts. 2009: 609-609. DOI: 10.1055/S-0029-1216708 |
0.586 |
|
2009 |
Davies HML, Sorensen EJ. Editorial: Rapid complexity generation in natural product total synthesis Chemical Society Reviews. 38: 2981-2982. DOI: 10.1039/B918568M |
0.404 |
|
2009 |
Schneekloth JS, Kim J,J, Sorensen EJ. An interrupted Ugi reaction enables the preparation of substituted indoxyls and aminoindoles Tetrahedron. 65: 3096-3101. DOI: 10.1016/j.tet.2008.08.055 |
0.551 |
|
2008 |
Seike H, Sorensen EJ. A Synthesis of the Tricyclic Core Structure of FR901483 Featuring an Ugi Four-Component Coupling and a Remarkably Selective Elimination Reaction. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2008: 695-701. PMID 22114366 DOI: 10.1055/S-2008-1042813 |
0.716 |
|
2008 |
Seike H, Sorensen EJ. A synthesis of the tricyclic core structure of FR901483 featuring an Ugi four-component coupling and a remarkably selective elimination reaction Synlett. 695-701. DOI: 10.1055/s-2008-1042813 |
0.679 |
|
2007 |
Keller S, Nicholson G, Drahl C, Sorensen E, Fiedler HP, Süssmuth RD. Abyssomicins G and H and atrop-abyssomicin C from the marine Verrucosispora strain AB-18-032. The Journal of Antibiotics. 60: 391-4. PMID 17617698 DOI: 10.1038/Ja.2007.54 |
0.777 |
|
2007 |
Evans MJ, Morris GM, Wu J, Olson AJ, Sorensen EJ, Cravatt BF. Mechanistic and structural requirements for active site labeling of phosphoglycerate mutase by spiroepoxides. Molecular Biosystems. 3: 495-506. PMID 17579775 DOI: 10.1039/B705113A |
0.31 |
|
2007 |
Buey RM, Calvo E, Barasoain I, Pineda O, Edler MC, Matesanz R, Cerezo G, Vanderwal CD, Day BW, Sorensen EJ, López JA, Andreu JM, Hamel E, Díaz JF. Cyclostreptin binds covalently to microtubule pores and lumenal taxoid binding sites. Nature Chemical Biology. 3: 117-25. PMID 17206139 DOI: 10.1038/Nchembio853 |
0.565 |
|
2007 |
Moreau RJ, Sorensen EJ. Classical carbonyl reactivity enables a short synthesis of the core structure of acutumine Tetrahedron. 63: 6446-6453. DOI: 10.1016/J.Tet.2007.03.024 |
0.778 |
|
2006 |
Hamel E, Day BW, Miller JH, Jung MK, Northcote PT, Ghosh AK, Curran DP, Cushman M, Nicolaou KC, Paterson I, Sorensen EJ. Synergistic effects of peloruside A and laulimalide with taxoid site drugs, but not with each other, on tubulin assembly. Molecular Pharmacology. 70: 1555-64. PMID 16887932 DOI: 10.1124/Mol.106.027847 |
0.404 |
|
2006 |
Jabbari A, Sorensen EJ, Houk KN. Transition states of the retro-ene reactions of allylic diazenes. Organic Letters. 8: 3105-7. PMID 16805563 DOI: 10.1021/Ol0612049 |
0.319 |
|
2006 |
Shipet WD, Sorensen EJ. Convergent, enantioselective syntheses of guanacastepenes A and E featuring a selective cyclobutane fragmentation Journal of the American Chemical Society. 128: 7025-7035. PMID 16719483 DOI: 10.1021/Ja060847G |
0.48 |
|
2006 |
Sorensen E, Shipe W. Syntheses of Guanacastepene E Synfacts. 2006: 1197-1197. DOI: 10.1055/s-2006-955593 |
0.71 |
|
2006 |
Zapf CW, Harrison BA, Drahl C, Sorensen EJ. Synthesis of Abyssomycin C Synfacts. 2006: 195-195. DOI: 10.1055/S-2006-931917 |
0.417 |
|
2006 |
Edler MC, Buey RM, Gussio R, Marcus AI, Vanderwal CD, Sorensen EJ, Díaz JF, Giannakakou P, Hamel E. Erratum: Cyclostreptin (FR182877), an antitumor tubulin-polymerizing agent deficient in enhancing tubulin assembly despite its high affinity for the taxoid site (Biochemistry (August 30, 2005) 44, 34 (11525-11538)) Biochemistry. 45. DOI: 10.1021/Bi068009M |
0.564 |
|
2006 |
Sorensen EJ, Theodorakis EA. Nature-inspired approaches to chemical synthesis Tetrahedron. 62: 5169. DOI: 10.1016/J.Tet.2006.02.084 |
0.634 |
|
2005 |
Zapf CW, Harrison BA, Drahl C, Sorensen EJ. A Diels-Alder macrocyclization enables an efficient asymmetric synthesis of the antibacterial natural product abyssomicin C. Angewandte Chemie (International Ed. in English). 44: 6533-7. PMID 16163781 DOI: 10.1002/Anie.200502119 |
0.821 |
|
2005 |
Drahl C, Cravatt BF, Sorensen EJ. Protein-reactive natural products. Angewandte Chemie (International Ed. in English). 44: 5788-809. PMID 16149114 DOI: 10.1002/Anie.200500900 |
0.774 |
|
2005 |
Edler MC, Buey RM, Gussio R, Marcus AI, Vanderwal CD, Sorensen EJ, Díaz JF, Giannakakou P, Hamel E. Cyclostreptin (FR182877), an antitumor tubulin-polymerizing agent deficient in enhancing tubulin assembly despite its high affinity for the taxoid site. Biochemistry. 44: 11525-38. PMID 16114889 DOI: 10.1021/Bi050660M |
0.592 |
|
2005 |
Sammis GM, Flamme EM, Xie H, Ho DM, Sorensen EJ. Design, synthesis, and reactivity of 1-hydrazinodienes for use in organic synthesis. Journal of the American Chemical Society. 127: 8612-3. PMID 15954764 DOI: 10.1021/Ja052383C |
0.82 |
|
2005 |
Alexanian EJ, Lee C, Sorensen EJ. Palladium-catalyzed ring-forming aminoacetoxylation of alkenes. Journal of the American Chemical Society. 127: 7690-1. PMID 15913354 DOI: 10.1021/Ja051406K |
0.731 |
|
2004 |
Sorensen EJ, Sammis GM. Chemistry. A dash of proline makes things sweet. Science (New York, N.Y.). 305: 1725-6. PMID 15375255 DOI: 10.1126/Science.1103026 |
0.761 |
|
2004 |
Stark LM, Pekari K, Sorensen EJ. A nucleophile-catalyzed cycloisomerization permits a concise synthesis of (+)-harziphilone Proceedings of the National Academy of Sciences of the United States of America. 101: 12064-12066. PMID 15232001 DOI: 10.1073/Pnas.0402563101 |
0.761 |
|
2004 |
Anderson EA, Alexanian EJ, Sorensen EJ. Synthesis of the furanosteroidal antibiotic viridin. Angewandte Chemie (International Ed. in English). 43: 1998-2001. PMID 15065284 DOI: 10.1002/Anie.200353129 |
0.766 |
|
2004 |
Vanderwal CD, Sorensen EJ. Chapter 1 A remarkable architectural self-construction process is discovered in a synthesis of FR182877 Strategies and Tactics in Organic Synthesis. 5: 1-50. DOI: 10.1016/S1874-6004(04)80024-8 |
0.665 |
|
2003 |
Adam GC, Vanderwal CD, Sorensen EJ, Cravatt BF. (-)-FR182877 is a potent and selective inhibitor of carboxylesterase-1. Angewandte Chemie (International Ed. in English). 42: 5480-4. PMID 14618582 DOI: 10.1002/Anie.200352576 |
0.574 |
|
2003 |
Sorensen EJ. Architectural self-construction in nature and chemical synthesis Bioorganic and Medicinal Chemistry. 11: 3225-3228. PMID 12837531 DOI: 10.1016/S0968-0896(03)00185-8 |
0.399 |
|
2003 |
Vanderwal CD, Vosburg DA, Weiler S, Sorensen EJ. An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursor. Journal of the American Chemical Society. 125: 5393-407. PMID 12720453 DOI: 10.1021/Ja021472B |
0.827 |
|
2003 |
Vosburg DA, Weiler S, Sorensen EJ. Concise stereocontrolled routes to fumagillol, fumagillin, and TNP-470. Chirality. 15: 156-66. PMID 12520508 DOI: 10.1002/Chir.10181 |
0.767 |
|
2003 |
Tamiya J, Sorensen EJ. A spontaneous bicyclization facilitates a synthesis of (-)-hispidospermidin Tetrahedron. 59: 6921-6932. DOI: 10.1016/S0040-4020(03)00936-0 |
0.817 |
|
2002 |
Shipe WD, Sorensen EJ. A Convergent Synthesis of the Tricyclic Architecture of the Guanacastepenes Featuring a Selective Ring Fragmentation Organic Letters. 4: 2063-2066. PMID 12049518 DOI: 10.1021/Ol0259342 |
0.821 |
|
2002 |
Vosburg DA, Vanderwal CD, Sorensen EJ. A synthesis of (+)-FR182877, featuring tandem transannular Diels-Alder reactions inspired by a postulated biogenesis. Journal of the American Chemical Society. 124: 4552-3. PMID 11971689 DOI: 10.1021/Ja025885O |
0.831 |
|
2001 |
Vanderwal CD, Vosburg DA, Sorensen EJ. Intramolecular allenolate acylations in studies toward a synthesis of FR182877. Organic Letters. 3: 4307-10. PMID 11784204 DOI: 10.1021/Ol016994V |
0.821 |
|
2001 |
Vanderwal CD, Vosburg DA, Sorensen EJ. Intramolecular allenolate acylations in studies toward a synthesis of FR182877 Organic Letters. 3: 4307-4310. DOI: 10.1021/ol016994v |
0.82 |
|
2000 |
Scheffler G, Seike H, Sorensen EJ. An Enantiospecific Synthesis of the Potent Immunosuppressant FR901483 Dr. G. Scheffler and H. Seike contributed equally to this work. We thank Dr. L. B. Pasternack and Dr. D. H. Huang for NMR spectroscopic assistance, and Dr. G. Siuzdak for mass spectrometric assistance. We also thank Dr. S. Takase and Dr. H. Setoi from the Fujisawa Pharmaceutical Co. for physical data for FR901483. This work was generously supported by The Skaggs Institute for Chemical Biology, a grant from the Merck Research Laboratories, a Beckman Young Investigator Award to E.J.S., and a predoctoral fellowship from the Heiwa Nakajima Foundation to H.S. Angewandte Chemie (International Ed. in English). 39: 4593-4596. PMID 11169681 DOI: 10.1002/1521-3773(20001215)39:24<4593::Aid-Anie4593>3.0.Co;2-X |
0.632 |
|
2000 |
Tamiya J, Sorensen EJ. A concise synthesis of (-)-hispidospermidin guided by a postulated biogenesis [10] Journal of the American Chemical Society. 122: 9556-9557. DOI: 10.1021/Ja0026758 |
0.81 |
|
2000 |
Scheffler G, Seike H, Sorensen EJ. An enantiospecific synthesis of the potent immunosuppressant FR901483 Angewandte Chemie - International Edition. 39: 4593-4596. DOI: 10.1002/1521-3773(20001215)39:24<4593::AID-ANIE4593>3.0.CO;2-X |
0.711 |
|
2000 |
Scheffler G, Seike H, Sorensen EJ. Eine enantioselektive Synthese des potenten Immunsuppressivums FR901483 Angewandte Chemie. 112: 4783-4785. DOI: 10.1002/1521-3757(20001215)112:24<4783::Aid-Ange4783>3.0.Co;2-X |
0.64 |
|
1999 |
Vosburg DA, Weiler S, Sorensen EJ. A Concise Synthesis of Fumagillol. Angewandte Chemie (International Ed. in English). 38: 971-974. PMID 29711854 DOI: 10.1002/(Sici)1521-3773(19990401)38:7<971::Aid-Anie971>3.0.Co;2-W |
0.724 |
|
1999 |
Vanderwal CD, Vosburg DA, Weiler S, Sorensen EJ. Postulated biogenesis of WS9885B and progress toward an enantioselective synthesis. Organic Letters. 1: 645-8. PMID 10823194 DOI: 10.1021/Ol990723R |
0.802 |
|
1999 |
Vosburg DA, Weiler S, Sorensen EJ. A concise synthesis of fumagillol Angewandte Chemie - International Edition. 38: 971-974. DOI: 10.1002/(SICI)1521-3773(19990401)38:7<971::AID-ANIE971>3.0.CO;2-W |
0.753 |
|
1999 |
Vosburg DA, Weiler S, Sorensen EJ. Eine kurze Synthese von Fumagillol Angewandte Chemie. 111: 1024-1027. DOI: 10.1002/(Sici)1521-3757(19990401)111:7<1024::Aid-Ange1024>3.0.Co;2-S |
0.718 |
|
1998 |
Nicolaou KC, Sorensen EJ, Winssinger N. The Art and Science of Organic and Natural Products Synthesis Journal of Chemical Education. 75: 1225-1258. DOI: 10.1021/Ed075P1225 |
0.631 |
|
1998 |
Nicolaou KC, Sorensen EJ, Winssinger N. The art and science of organic and natural products synthesis Journal of Chemical Education. 75: 1226-1258. |
0.548 |
|
1997 |
Meng D, Bertinato P, Balog A, Su DS, Kamenecka T, Sorensen EJ, Danishefsky SJ. Total syntheses of epothilones A and B Journal of the American Chemical Society. 119: 10073-10092. DOI: 10.1021/Ja971946K |
0.392 |
|
1997 |
Meng D, Su DS, Balog A, Bertinato P, Sorensen EJ, Danishefsky SJ, Zheng YH, Chou TC, He L, Horwitz SB. Remote effects in macrolide formation through ring-forming olefin metathesis: An application to the synthesis of fully active epothilone congeners Journal of the American Chemical Society. 119: 2733-2734. DOI: 10.1021/Ja964275J |
0.577 |
|
1997 |
Balog A, Bertinato P, Su DS, Meng D, Sorensen E, Danishefsky SJ, Zheng YH, Chou TC, He L, Horwitz SB. Stereoselective syntheses and evaluation of compounds in the 8-desmethylepothilone a series: Some surprising observations regarding their chemical and biological properties Tetrahedron Letters. 38: 4529-4532. DOI: 10.1016/S0040-4039(97)00931-3 |
0.473 |
|
1997 |
Su D, Meng D, Bertinato P, Balog A, Sorensen EJ, Danishefsky SJ, Chou T, He L, Horwitz SB. Totalsynthese von ( - )-Epothilon B: eine Erweiterung der Suzuki-Kupplung und Erkenntnisse über Struktur-Wirkungs-Beziehungen der Epothilone Angewandte Chemie. 109: 775-777. DOI: 10.1002/Ange.19971090719 |
0.397 |
|
1996 |
Bertinato P, Sorensen EJ, Meng D, Danishefsky SJ. Studies toward a Synthesis of Epothilone A: Stereocontrolled Assembly of the Acyl Region and Models for Macrocyclization. The Journal of Organic Chemistry. 61: 8000-8001. PMID 11667778 |
0.454 |
|
1996 |
Meng D, Sorensen EJ, Bertinato P, Danishefsky SJ. Studies toward a Synthesis of Epothilone A: Use of Hydropyran Templates for the Management of Acyclic Stereochemical Relationships. The Journal of Organic Chemistry. 61: 7998-7999. PMID 11667777 DOI: 10.1021/Jo961673W |
0.495 |
|
1996 |
Bertinato P, Sorensen EJ, Meng D, Danishefsky SJ. Studies toward a synthesis of epothilone A: Stereocontrolled assembly of the acyl region and models for macrocyclization Journal of Organic Chemistry. 61: 8000-8001. DOI: 10.1021/jo961674o |
0.454 |
|
1996 |
Meng D, Sorensen EJ, Bertinato P, Danishefsky SJ. Studies toward a synthesis of epothilone A: Use of hydropyran templates for the management of acyclic stereochemical relationships Journal of Organic Chemistry. 61: 7998-7999. DOI: 10.1021/jo961673w |
0.423 |
|
1996 |
Balog A, Meng D, Kamenecka T, Bertinato P, Su D, Sorensen EJ, Danishefsky SJ. Total Synthesis of (–)‐Epothilone A Angewandte Chemie. 35: 2801-2803. DOI: 10.1002/Anie.199628011 |
0.429 |
|
1996 |
Balog A, Meng D, Kamenecka T, Bertinato P, Su D, Sorensen EJ, Danishefsky SJ. Totalsynthese von (—)-Epothilon A Angewandte Chemie. 108: 2976-2978. DOI: 10.1002/Ange.19961082318 |
0.366 |
|
1996 |
Balog A, Meng D, Kamenecka T, Bertinato P, Su DS, Sorensen EJ, Danishefsky SJ. Total synthesis of (-)-epothilone A Angewandte Chemie - International Edition in English. 35: 2801-2803. |
0.371 |
|
1995 |
Nicolaou KC, Liu J, Yang Z, Ueno H, Sorensen EJ, Claiborne CF, Guy RK, Hwang C, Nakada M, Nantermet PG. Total synthesis of Taxol. 2. construction of A and C ring intermediates and initial attempts to construct the ABC ring system. [Erratum to document cited in CA122:160984] Journal of the American Chemical Society. 117: 8690-8690. DOI: 10.1021/Ja00138A035 |
0.666 |
|
1995 |
Nicolaou KC, Liu JJ, Yang Z, Ueno H, Sorensen EJ, Claiborne CF, Guy RK, Hwang CK, Nakada M, Nantermet PG. Total synthesis of Taxol. 2. Construction of A and C ring intermediates and initial attempts to construct the ABC ring system Journal of the American Chemical Society. 117: 634-644. DOI: 10.1021/Ja00107A007 |
0.683 |
|
1995 |
Nicolaou KC, Nantermet PG, Ueno H, Guy RK, Couladouros EA, Sorensen EJ. Total synthesis of Taxol. 1. Retrosynthesis, degradation, and reconstitution Journal of the American Chemical Society. 117: 624-633. DOI: 10.1021/Ja00107A006 |
0.67 |
|
1994 |
Nicolaou KC, Claiborne CF, Nantermet PG, Couladouros EA, Sorensen EJ. Synthesis of Novel Taxoids Journal of the American Chemical Society. 116: 1591-1592. DOI: 10.1021/Ja00083A063 |
0.589 |
|
1994 |
Nicolaou KC, Claiborne CF, Nantermet PG, Couladouros EA, Sorensen EJ. Synthesis of novel taxoids Journal of the American Chemical Society. 116: 1591-1592. |
0.393 |
|
1993 |
Nicolaou KC, Yang Z, Sorensen EJ, Nakada M. Synthesis of ABC taxoid ring systems via a convergent strategy Journal of the Chemical Society, Chemical Communications. 1024-1026. DOI: 10.1039/C39930001024 |
0.59 |
|
1992 |
Nicolaou KC, Hwang CK, Sorensen EJ, Clairborne CF. A convergent strategy towards taxol. A facile enantioselective entry into a fully functionalized ring A system Journal of the Chemical Society - Series Chemical Communications. 1117-1118. DOI: 10.1039/C39920001117 |
0.409 |
|
1992 |
Nicolaou KC, Sorensen EJ, Discordia R, Hwang C, Bergman RG, Minto RE, Bharucha KN. Ten-Membered Ring Enediynes with Remarkable Chemical and Biological Profiles Angewandte Chemie International Edition in English. 31: 1044-1046. DOI: 10.1002/Anie.199210441 |
0.451 |
|
1992 |
Nicolaou KC, Sorensen EJ, Discordia R, Hwang C, Minto RE, Bharucha KN, Bergman RG. Zehngliedrige cyclische Endiine mit bemerkenswerten chemischen und biologischen Eigenschaften Angewandte Chemie. 104: 1094-1096. DOI: 10.1002/Ange.19921040838 |
0.336 |
|
Show low-probability matches. |