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Paul A. Clarke, Ph.D - Publications

1996-1999 Chemistry Florida State University, Tallahassee, FL, United States 
 1999-1999 Chemistry University of Exeter, Exeter, England, United Kingdom 
 1999-2006 Chemistry University of Nottingham, Nottingham, England, United Kingdom 
 2006- Chemistry University of York, York, England, United Kingdom 
Natural product synthesis

27 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
2020 Hawkins K, Patterson A, Clarke PA, Smith DK. Catalytic Gels for a Prebiotically-Relevant Asymmetric Aldol Reaction in Water: From Organocatalyst Design to Hydrogel Discovery and Back Again. Journal of the American Chemical Society. PMID 32023044 DOI: 10.1021/Jacs.9B13156  0.335
2018 Griggs SD, Thompson N, Tape DT, Fabre M, Clarke PA. Correction: Synthesis of highly substituted 2-spiropiperidines. Organic & Biomolecular Chemistry. PMID 30095852 DOI: 10.1039/C8Ob90117A  0.301
2018 Griggs SD, Thompson N, Tape DT, Fabre M, Clarke PA. Synthesis of highly substituted 2-spiropiperidines. Organic & Biomolecular Chemistry. PMID 30067258 DOI: 10.1039/C8Ob01272E  0.383
2017 Steer AM, Bia N, Smith DK, Clarke PA. Prebiotic synthesis of 2-deoxy-d-ribose from interstellar building blocks promoted by amino esters or amino nitriles. Chemical Communications (Cambridge, England). PMID 28884758 DOI: 10.1039/C7Cc06083A  0.32
2017 Griggs SD, Thompson N, Tape DT, Fabre M, Clarke PA. A Two-Step Synthesis of 2-Spiropiperidines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28561323 DOI: 10.1002/Chem.201702467  0.316
2017 Ermanis K, Hsiao YT, Kaya U, Jeuken A, Clarke PA. The stereodivergent formation of 2,6-cis and 2,6-trans-tetrahydropyrans: experimental and computational investigation of the mechanism of a thioester oxy-Michael cyclization. Chemical Science. 8: 482-490. PMID 28451195 DOI: 10.1039/C6Sc03478K  0.322
2016 Clarke PA, Nasir NM, Sellars PB, Peter AM, Lawson CA, Burroughs JL. Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland-Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B. Organic & Biomolecular Chemistry. PMID 27340028 DOI: 10.1039/C6Ob01182A  0.357
2015 Rayner PJ, Smith JC, Denneval C, O'Brien P, Clarke PA, Horan RA. Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine. Chemical Communications (Cambridge, England). PMID 26620913 DOI: 10.1039/C5Cc08690F  0.303
2012 Clarke PA, Mistry N, Thomas GH. Synthesis of the complete series of mono acetates of N-acetyl-D-neuraminic acid. Organic & Biomolecular Chemistry. 10: 529-35. PMID 22095310 DOI: 10.1039/C1Ob06348K  0.311
2011 Iqbal M, Black RJ, Winn J, Reeder AT, Blake AJ, Clarke PA. Studies on transannulation reactions across a nine-membered ring: the synthesis of natural product-like structures. Organic & Biomolecular Chemistry. 9: 5062-78. PMID 21597625 DOI: 10.1039/C1Ob05448A  0.342
2011 Clarke PA, Santos S, Mistry N, Burroughs L, Humphries AC. The asymmetric Maitland-Japp reaction and its application to the construction of the C1-C19 bis-pyran unit of phorboxazole B. Organic Letters. 13: 624-7. PMID 21247215 DOI: 10.1021/Ol102860R  0.321
2011 Clarke PA, Winn J. Synthesis of an austrodorane sesquiterpenoid core via a transannular Prins cyclization Tetrahedron Letters. 52: 1469-1472. DOI: 10.1016/J.Tetlet.2011.01.093  0.325
2009 Clarke PA, Cridland AP, Rolla GA, Iqbal M, Bainbridge NP, Whitwood AC, Wilson C. Studies on the synthesis of the ABC rings of (+/-)-hexacyclinic acid. The Journal of Organic Chemistry. 74: 7812-21. PMID 19813768 DOI: 10.1021/Jo901547K  0.341
2008 Clarke PA, Zaytsev AV, Morgan TW, Whitwood AC, Wilson C. One-pot synthesis of functionalized piperid-4-ones: a four-component condensation. Organic Letters. 10: 2877-80. PMID 18533668 DOI: 10.1021/Ol801051G  0.324
2007 Clarke PA, Santos S, Martin WHC. Combining pot, atom and step economy (PASE) in organic synthesis. Synthesis of tetrahydropyran-4-ones Green Chemistry. 9: 438-440. DOI: 10.1039/B700923B  0.477
2005 Clarke PA, Martin WH, Hargreaves JM, Wilson C, Blake AJ. The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland-Japp reaction. Organic & Biomolecular Chemistry. 3: 3551-63. PMID 16172694 DOI: 10.1039/B508252H  0.513
2005 Clarke PA, Martin WH, Hargreaves JM, Wilson C, Blake AJ. Revisiting the Maitland-Japp reaction. Concise construction of highly functionalised tetrahydropyran-4-ones. Chemical Communications (Cambridge, England). 1061-3. PMID 15719116 DOI: 10.1039/B416247A  0.502
2005 Clarke PA, Martin WHC. Exploiting the Maitland-Japp reaction: A synthesis of (±)- centrolobine Tetrahedron. 61: 5433-5438. DOI: 10.1016/J.Tet.2005.04.011  0.482
2005 Clarke PA, Martin WHC. Exploiting the Maitland—Japp Reaction: A Synthesis of (.+-.)-Centrolobine Cheminform. 36. DOI: 10.1002/chin.200541206  0.455
2005 Clarke PA, Martin WHC. An Expedient Synthesis of (.+-.)-Centrolobine. Cheminform. 36. DOI: 10.1002/chin.200513235  0.416
2004 Clarke PA, Martin WHC. An expedient synthesis of (±)-centrolobine Tetrahedron Letters. 45: 9061-9063. DOI: 10.1016/J.Tetlet.2004.10.035  0.498
2003 Clarke PA, Martin WHC. Synthetic methods: Part (v) protecting groups Annual Reports On the Progress of Chemistry - Section B. 99: 84-103. DOI: 10.1039/B212008A  0.331
2002 Clarke PA, Martin WH. Diastereoselective synthesis of highly substituted tetrahydropyran-4-ones. Organic Letters. 4: 4527-9. PMID 12465929 DOI: 10.1021/Ol027081J  0.515
2002 Clarke PA, Kayaleh NE, Smith MA, Baker JR, Bird SJ, Chan C. A one-step procedure for the monoacylation of symmetrical 1,2-diols. The Journal of Organic Chemistry. 67: 5226-31. PMID 12126410 DOI: 10.1021/Jo0257041  0.324
2000 Buck RT, Clarke PA, Coe DM, Drysdale MJ, Ferris L, Haigh D, Moody CJ, Pearson ND, Swann E. The carbenoid approach to peptide synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 2160-7. PMID 10926221 DOI: 10.1002/1521-3765(20000616)6:12<2160::Aid-Chem2160>3.0.Co;2-Y  0.343
1996 Armstrong A, Barsanti PA, Clarke PA, Wood A. Ketone-directed peracid epoxidation of cyclic alkenes Journal of the Chemical Society - Perkin Transactions 1. 1373-1380. DOI: 10.1039/P19960001373  0.536
1996 Armstrong A, Clarke PA, Wood A. Evidence that a dioxirane is not responsible for alkene epoxidation in a ketone–Oxone® system Chemical Communications. 849-850. DOI: 10.1039/Cc9960000849  0.486
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