Year |
Citation |
Score |
2023 |
Pettus TR. Nucleophilic Addition of 4,5-Dihydrooxazole Derivatives to Base Generated o-Quinone Methides: A Four-Component Reaction The Journal of Organic Chemistry. 88: 2583-2588. DOI: 10.1021/acs.joc.2c02614 |
0.461 |
|
2019 |
Pettus TR. Nucleophilic Imines and Electrophilic o-Quinone Methides, a Three-Component Assembly of Assorted 3,4-Dihydro-2H-1,3-benzoxazines Organic Letters. DOI: 10.1021/acs.orglett.9b02655 |
0.376 |
|
2018 |
Pettus T, Feng Z, Burnett G. A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519. DOI: 10.1055/s-0036-1592001 |
0.443 |
|
2018 |
Pettus T, Feng Z, Burnett G. A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519. DOI: 10.1055/s-0036-1592001 |
0.443 |
|
2018 |
Pettus T, Feng Z, Burnett G. A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519. DOI: 10.1055/S-0036-1592001 |
0.801 |
|
2018 |
Pettus T, Feng Z, Burnett G. A Biomimetic Synthesis of des-Hydroxy Paecilospirone Synlett. 29: 1517-1519. DOI: 10.1055/S-0036-1592001 |
0.801 |
|
2015 |
Feng ZG, Bai WJ, Pettus TR. Unified total syntheses of (-)-medicarpin, (-)-sophoracarpan A, and (±)-kushecarpin A with some structural revisions. Angewandte Chemie (International Ed. in English). 54: 1864-7. PMID 25476784 DOI: 10.1002/Anie.201408910 |
0.767 |
|
2014 |
Bai WJ, David JG, Feng ZG, Weaver MG, Wu KL, Pettus TR. The domestication of ortho-quinone methides. Accounts of Chemical Research. 47: 3655-64. PMID 25469551 DOI: 10.1021/Ar500330X |
0.829 |
|
2014 |
David JG, Bai WJ, Weaver MG, Pettus TR. A general diastereoselective catalytic vinylogous aldol reaction among tetramic acid-derived pyrroles. Organic Letters. 16: 4384-7. PMID 25119431 DOI: 10.1021/Ol501715R |
0.764 |
|
2014 |
Weaver MG, Bai WJ, Jackson SK, Pettus TR. Diels-Alder construction of regiodifferentiated meta-amino phenols and derivatives. Organic Letters. 16: 1294-7. PMID 24524325 DOI: 10.1021/Ol4034447 |
0.78 |
|
2012 |
Green JC, Burnett GL, Pettus TR. New strategies for natural products containing chroman spiroketals. Pure and Applied Chemistry. Chimie Pure Et Appliquee. 84: 1621-1631. PMID 25554712 DOI: 10.1351/Pac-Con-11-10-34 |
0.723 |
|
2012 |
Bai WJ, Jackson SK, Pettus TR. Mild construction of 3-methyl tetramic acids enabling a formal synthesis of palau'imide. Organic Letters. 14: 3862-5. PMID 22804621 DOI: 10.1021/Ol301556A |
0.725 |
|
2012 |
Green JC, Brown ER, Pettus TR. Intramolecular condensation via an o-quinone methide: total synthesis of (±)-heliol. Organic Letters. 14: 2929-31. PMID 22650973 DOI: 10.1021/Ol301092W |
0.751 |
|
2012 |
Cohn EP, Wu KL, Pettus TR, Reich NO. A new strategy for detection and development of tractable telomerase inhibitors. Journal of Medicinal Chemistry. 55: 3678-86. PMID 22413845 DOI: 10.1021/Jm201191D |
0.655 |
|
2012 |
Bai WJ, Green JC, Pettus TR. Total syntheses of ent-heliespirones A and C. The Journal of Organic Chemistry. 77: 379-87. PMID 22074003 DOI: 10.1021/Jo201971G |
0.721 |
|
2011 |
Green JC, Jiménez-Alonso S, Brown ER, Pettus TR. Total synthesis and repudiation of the helianane family. Organic Letters. 13: 5500-3. PMID 21928811 DOI: 10.1021/Ol2022214 |
0.799 |
|
2011 |
Wu KL, Mercado EV, Pettus TR. A convergent total synthesis of (±)-γ-rubromycin. Journal of the American Chemical Society. 133: 6114-7. PMID 21452818 DOI: 10.1021/Ja1115524 |
0.635 |
|
2011 |
Cha JY, Burnett GL, Huang Y, Davidson JB, Pettus TR. A strategy for the late-stage divergent syntheses of scyphostatin analogues. The Journal of Organic Chemistry. 76: 1361-71. PMID 21250721 DOI: 10.1021/Jo102327E |
0.751 |
|
2011 |
Green JC, Pettus TR. An oxidative dearomatization-induced [5 + 2] cascade enabling the syntheses of α-cedrene, α-pipitzol, and sec-cedrenol. Journal of the American Chemical Society. 133: 1603-8. PMID 21194216 DOI: 10.1021/Ja109925G |
0.671 |
|
2011 |
Wenderski TA, Marsini MA, Pettus TR. A diastereoselective formal synthesis of berkelic acid. Organic Letters. 13: 118-21. PMID 21138313 DOI: 10.1021/Ol102652T |
0.842 |
|
2010 |
Wenderski TA, Hoarau C, Mejorado L, Pettus TR. Dearomatization applications of I((III)) reagents and some unusual reactivity amongst resorcinol derived cyclohexadienones. Tetrahedron. 66: 5873-5883. PMID 23750053 DOI: 10.1016/J.Tet.2010.05.041 |
0.803 |
|
2009 |
Wenderski TA, Denatale V, Pettus TR. Synthesis of 2,2-Disubstituted Pentalenes and Indenes by a Useful Modification to Nakamura's DMCP [3+2]-Cycloaddition Protocol. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 16: 2637-2642. PMID 21442051 DOI: 10.1055/S-0029-1217755 |
0.817 |
|
2009 |
Cha JY, Huang Y, Pettus TR. Total synthesis of TK-57-164A, isariotin F, and their putative progenitor isariotin E. Angewandte Chemie (International Ed. in English). 48: 9519-21. PMID 19921667 DOI: 10.1002/Anie.200904716 |
0.574 |
|
2009 |
Wenderski TA, Huang S, Pettus TR. Enantioselective total synthesis of all of the known chiral cleroindicins (C-F): clarification among optical rotations and assignments. The Journal of Organic Chemistry. 74: 4104-9. PMID 19476394 DOI: 10.1021/Jo900401K |
0.798 |
|
2009 |
Miller LA, Marsini MA, Pettus TR. Chemoselective reactions of 3-benzyloxy-1,2-o-quinone with organometallic reagents. Organic Letters. 11: 1955-8. PMID 19331343 DOI: 10.1021/Ol9004068 |
0.814 |
|
2009 |
Pettus T, Pettus L. Intermolecular Applications of o-Quinone Methides (o-QMs) Anionically Generated at Low Temperatures: Kinetic Conditions Quinone Methides. 89-117. DOI: 10.1002/9780470452882.ch4 |
0.796 |
|
2008 |
Huang Y, Pettus TR. A Cycloaddition Strategy for Use toward Berkelic Acid, an MMP Inhibitor and Potent Anticancer Agent Displaying a Unique Chroman Spiroketal Motif. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 9: 1353-1356. PMID 19183702 DOI: 10.1055/S-2008-1072750 |
0.611 |
|
2008 |
Marsini MA, Huang Y, Lindsey CC, Wu KL, Pettus TR. Diastereoselective syntheses of chroman spiroketals via [4 + 2] cycloaddition of enol ethers and o-quinone methides. Organic Letters. 10: 1477-80. PMID 18336038 DOI: 10.1021/Ol8003244 |
0.817 |
|
2008 |
Pettus T, Wenderski T. Chapter 13 Seduced by a siren's call: expanding applications for aromatic compounds and the synthesis of (+)-rishirilide B Strategies and Tactics in Organic Synthesis. 7: 460-490. DOI: 10.1016/S1874-6004(08)80017-2 |
0.829 |
|
2007 |
Wu KL, Wilkinson S, Reich NO, Pettus TR. Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition. Organic Letters. 9: 5537-40. PMID 18044909 DOI: 10.1021/Ol702450D |
0.582 |
|
2007 |
Marsini MA, Huang Y, Van De Water RW, Pettus TR. Synthesis of resorcinol derived spironitronates. Organic Letters. 9: 3229-32. PMID 17645344 DOI: 10.1021/Ol0710257 |
0.808 |
|
2007 |
Pettus T, Mejorado L. Synthesis of (+)-Rishirilide B Synfacts. 2007: 0463-0463. DOI: 10.1055/s-2007-968399 |
0.371 |
|
2007 |
Pettus T, Mejorado L. Synthesis of (+)-Rishirilide B Synfacts. 2007: 0463-0463. DOI: 10.1055/S-2007-968399 |
0.791 |
|
2007 |
Pettus T, Mejorado L. Synthesis of (+)-Rishirilide B Synfacts. 2007: 0463-0463. DOI: 10.1055/s-2007-968399 |
0.371 |
|
2007 |
Pettus T, Mejorado L. Synthesis of (+)-Rishirilide B Synfacts. 2007: 0463-0463. DOI: 10.1055/s-2007-968399 |
0.371 |
|
2007 |
Pettus T, Mejorado L. Synthesis of (+)-Rishirilide B Synfacts. 2007: 0463-0463. DOI: 10.1055/S-2007-968399 |
0.791 |
|
2006 |
Selenski C, Pettus TR. (±)-Diinsininone: made nature's way. Tetrahedron. 62: 5298-5307. PMID 19079766 DOI: 10.1016/J.Tet.2006.01.109 |
0.819 |
|
2006 |
Mejorado L, Pettus TR. Diastereoselective Synthesis of a Simplified Core of Rishirilide B. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 3209-3214. PMID 18846264 DOI: 10.1055/S-2006-950188 |
0.835 |
|
2006 |
Lindsey CC, Pettus TR. Unusual cycloadditions of o-quinone methides with oxazoles. Tetrahedron Letters. 47: 201-204. PMID 18592015 DOI: 10.1016/J.Tetlet.2005.10.168 |
0.716 |
|
2006 |
Mejorado LH, Pettus TR. Total synthesis of (+)-rishirilide B: development and application of general processes for enantioselective oxidative dearomatization of resorcinol derivatives. Journal of the American Chemical Society. 128: 15625-31. PMID 17147370 DOI: 10.1021/Ja062987W |
0.857 |
|
2006 |
Marsini MA, Gowin KM, Pettus TR. Total synthesis of (+/-)-mitorubrinic acid. Organic Letters. 8: 3481-3. PMID 16869640 DOI: 10.1021/Ol0610993 |
0.798 |
|
2006 |
Hoarau C, Pettus TR. General synthesis for chiral 4-alkyl-4-hydroxycyclohexenones. Organic Letters. 8: 2843-6. PMID 16774271 DOI: 10.1021/Ol061000S |
0.693 |
|
2006 |
Lindsey CC, Wu KL, Pettus TR. Synthesis of electron deficient 5,6-aryloxy spiroketals. Organic Letters. 8: 2365-7. PMID 16706527 DOI: 10.1021/Ol0606886 |
0.741 |
|
2006 |
Pettus T, Huang Y, Zhang J. Synthesis of (±)-Brazilin Synfacts. 2006: 0424-0424. DOI: 10.1055/s-2006-934391 |
0.311 |
|
2006 |
Pettus T, Huang Y, Zhang J. Synthesis of (±)-Brazilin Synfacts. 2006: 0424-0424. DOI: 10.1055/s-2006-934391 |
0.311 |
|
2006 |
Pettus T, Huang Y, Zhang J. Synthesis of (±)-Brazilin Synfacts. 2006: 0424-0424. DOI: 10.1055/s-2006-934391 |
0.594 |
|
2006 |
Pettus T, Huang Y, Zhang J. Synthesis of (±)-Brazilin Synfacts. 2006: 0424-0424. DOI: 10.1055/s-2006-934391 |
0.311 |
|
2006 |
Pettus T, Huang Y, Zhang J. Synthesis of (±)-Brazilin Synfacts. 2006: 0424-0424. DOI: 10.1055/S-2006-934391 |
0.515 |
|
2005 |
Huang Y, Zhang J, Pettus TR. Synthesis of (+/-)-brazilin using IBX. Organic Letters. 7: 5841-4. PMID 16354080 DOI: 10.1021/Ol0523749 |
0.785 |
|
2004 |
McQuaid KM, Pettus TR. Chemoselective Epoxidation of Electron Deficient Enones with Iodosylbenzene. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 13: 2403-2405. PMID 19079634 DOI: 10.1055/S-2004-832814 |
0.675 |
|
2004 |
Selenski C, Pettus TR. Enantioselective [4 + 2] cycloadditions of o-quinone methides: total synthesis of (+)-mimosifoliol and formal synthesis of (+)-tolterodine. The Journal of Organic Chemistry. 69: 9196-203. PMID 15609955 DOI: 10.1021/Jo048703C |
0.845 |
|
2004 |
Mejorado LH, Hoarau C, Pettus TR. Diastereoselective dearomatization of resorcinols directed by a lactic acid tether: unprecedented enantioselective access to p-quinols. Organic Letters. 6: 1535-8. PMID 15128229 DOI: 10.1021/Ol0498592 |
0.818 |
|
2004 |
Magdziak D, Meek SJ, Pettus TR. Cyclohexadienone ketals and quinols: four building blocks potentially useful for enantioselective synthesis. Chemical Reviews. 104: 1383-430. PMID 15008626 DOI: 10.1021/Cr0306900 |
0.791 |
|
2003 |
Hoarau C, Pettus TR. Strategies for the Preparation of Differentially Protected ortho-Prenylated Phenols. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 127-137. PMID 18563206 DOI: 10.1055/S-2003-36234 |
0.668 |
|
2002 |
Jones RM, Selenski C, Pettus TR. Rapid syntheses of benzopyrans from o-OBOC salicylaldehydes and salicyl alcohols: a three-component reaction. The Journal of Organic Chemistry. 67: 6911-5. PMID 12353982 DOI: 10.1021/Jo020224V |
0.821 |
|
2002 |
Magdziak D, Rodriguez AA, Van De Water RW, Pettus TR. Regioselective oxidation of phenols to o-quinones with o-iodoxybenzoic acid (IBX). Organic Letters. 4: 285-8. PMID 11796071 DOI: 10.1021/Ol017068J |
0.793 |
|
2001 |
Jones RM, Van De Water RW, Lindsey CC, Hoarau C, Ung T, Pettus TR. A mild anionic method for generating o-quinone methides: facile preparations of ortho-functionalized phenols. The Journal of Organic Chemistry. 66: 3435-41. PMID 11348127 DOI: 10.1021/Jo001752E |
0.783 |
|
2001 |
Pettus LH, Van De Water RW, Pettus TR. Synthesis of (+/-)-epoxysorbicillinol using a novel cyclohexa-2,5-dienone with synthetic applications to other sorbicillin derivatives. Organic Letters. 3: 905-8. PMID 11263912 DOI: 10.1021/Ol0155438 |
0.836 |
|
2001 |
Magdziak D, Pettus LH, Pettus TR. Enantioselective hydride abstraction in organic substrates: a novel use for chiral carbenium ions. Organic Letters. 3: 557-9. PMID 11178824 DOI: 10.1021/Ol006963K |
0.788 |
|
2000 |
Martello LA, McDaid HM, Regl DL, Yang CP, Meng D, Pettus TR, Kaufman MD, Arimoto H, Danishefsky SJ, Smith AB, Horwitz SB. Taxol and discodermolide represent a synergistic drug combination in human carcinoma cell lines. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 6: 1978-87. PMID 10815923 |
0.401 |
|
1998 |
Chen X, Zhou B, Bhattacharya S, Gutteridge C, Pettus T, Danishefsky S. Totalsynthese von Eleutherobin: zum Schluß eine Überraschung Angewandte Chemie. 110: 835-838. DOI: 10.1002/(Sici)1521-3757(19980316)110:6<835::Aid-Ange835>3.0.Co;2-0 |
0.724 |
|
1998 |
Chen X, Gutteridge C, Bhattacharya S, Zhou B, Pettus T, Hascall T, Danishefsky S. Eine konvergente Route zur Totalsynthese der Eleutheside Angewandte Chemie. 110: 195-197. DOI: 10.1002/(Sici)1521-3757(19980116)110:1/2<195::Aid-Ange195>3.0.Co;2-C |
0.75 |
|
1989 |
Hudlicky T, Seoane G, Pettus T. Enantioselective synthesis of (-)-zeylena from styrene Journal of Organic Chemistry. 54: 4239-4243. DOI: 10.1021/Jo00278A052 |
0.539 |
|
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