Ian Paterson
Affiliations: | Chemistry | University of Cambridge, Cambridge, England, United Kingdom |
Area:
Asymmetric synthesisWebsite:
http://www-paterson.ch.cam.ac.uk/index.htmlGoogle:
"Ian Paterson"Mean distance: 7.11
Parents
Sign in to add mentor| Ian Fleming | grad student | 1976-1979 | Cambridge |
| Gilbert Stork | post-doc | Columbia |
Children
Sign in to add trainee| Mark Coster | grad student | Cambridge | |
| Jonathan M. Goodman | grad student | Cambridge | |
| Jennifer Kan | grad student | Cambridge | |
| Cynthia McClure | grad student | Cambridge | |
| Simon B. Blakey | grad student | 1997-2002 | Cambridge |
| Mike Housden | grad student | 2007-2011 | Cambridge |
| Sarah J. Fink | grad student | 2008-2012 | Cambridge |
| Nelson Y. S. Lam | grad student | 2015-2019 | Cambridge |
| David Berrisford | post-doc | Cambridge | |
| Prabhat Arya | post-doc | 1986-1987 | Cambridge |
| Robert Britton | post-doc | 2002-2004 | Cambridge |
| Dirk Menche | post-doc | 2002-2004 | Cambridge |
| Gaelle Chouraqui | post-doc | 2005-2006 | Cambridge |
BETA: Related publications
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Publications
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| Muir G, Paterson I, Lam NYS, et al. (2024) Synthesis of the Phormidolide A Macrocycle Supports the Proposed Configurational Reassignment. Organic Letters |
| Estévez-Gallego J, Álvarez-Bernad B, Pera B, et al. (2022) Chemical modulation of microtubule structure through the laulimalide/peloruside site. Structure (London, England : 1993) |
| Stockdale TP, Lam NYS, Paterson I. (2022) A synthesis-enabled relative configurational assignment of the C31-C46 region of hemicalide. Chemical Communications (Cambridge, England) |
| Ndukwe IE, Wang X, Lam NYS, et al. (2020) Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A. Chemical Communications (Cambridge, England) |
| Pettigrew TR, Porter RJ, Walsh SJ, et al. (2020) Total synthesis and biological evaluation of simplified aplyronine analogues as synthetically tractable anticancer agents. Chemical Communications (Cambridge, England) |
| Anketell M, Sharrock T, Paterson I. (2019) A Unified Total Synthesis of the Actinoallolides, a Family of Potent Anti-trypanosomal Macrolides. Angewandte Chemie (International Ed. in English) |
| Lam NYS, Muir G, Challa VR, et al. (2019) A counterintuitive stereochemical outcome from a chelation-controlled vinylmetal aldehyde addition leads to the configurational reassignment of phormidolide A. Chemical Communications (Cambridge, England) |
| Lam NYS, Paterson I. (2019) Stereocontrolled Synthesis as an Enabling Tool for the Configurational Assignment of Marine Polyketide Natural Products European Journal of Organic Chemistry. 2020: 2310-2320 |
| Phillips AW, Anketell MJ, Balan T, et al. (2018) Toward the total synthesis of patellazole B: synthesis of an advanced C1-C25 fragment corresponding to the macrocyclic skeleton. Organic & Biomolecular Chemistry |
| Han BY, Lam NYS, MacGregor CI, et al. (2018) A synthesis-enabled relative stereochemical assignment of the C1-C28 region of hemicalide. Chemical Communications (Cambridge, England) |