Robert Britton
Affiliations: | Simon Fraser University, Burnaby, British Columbia, Canada |
Area:
organic chemistryGoogle:
"Robert Britton"Mean distance: 8.99 | S | N | B | C | P |
Parents
Sign in to add mentorVictor A. Snieckus | research assistant | 1991-1996 | University of Waterloo |
Edward Piers | grad student | 1996-2002 | UBC |
Ian Paterson | post-doc | 2002-2004 | Cambridge |
Children
Sign in to add traineeBaldip Kang | grad student | 2012 | Simon Fraser |
Jeffrey S. Mowat | grad student | 2012 | Simon Fraser |
James D. Senior | post-doc | Simon Fraser | |
Bharanishashank Adluri | post-doc | 2016-2018 | Simon Fraser |
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Publications
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Kaghad A, Panagopoulos D, Caballero-García G, et al. (2023) An α-chloroaldehyde-based formal synthesis of eribulin. Nature Communications. 14: 1904 |
Davison EK, Petrone DA, Meanwell M, et al. (2022) Practical and concise synthesis of nucleoside analogs. Nature Protocols |
Meanwell M, Fehr G, Ren W, et al. (2021) Diversity-oriented synthesis of glycomimetics. Communications Chemistry. 4: 96 |
Challa VR, Kwon D, Taron M, et al. (2021) Total synthesis of biselide A. Chemical Science. 12: 5534-5543 |
Meanwell M, Silverman SM, Lehmann J, et al. (2020) A short de novo synthesis of nucleoside analogs. Science (New York, N.Y.). 369: 725-730 |
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) |
Newton JJ, Jelier BJ, Meanwell M, et al. (2020) Quaternary Ammonium Trifluoromethoxide Salts as Stable Sources of Nucleophilic OCF. Organic Letters |
Ren W, Farren-Dai M, Sannikova N, et al. (2020) Glycoside Hydrolase Stabilization of Transition State Charge: New Directions for Inhibitor Design Chemical Science |
Newton J, Driedger D, Nodwell MB, et al. (2019) A Convenient Synthesis of Difluoroalkyl Ethers from Thionoesters using Silver(I) Fluoride. Chemistry (Weinheim An Der Bergstrasse, Germany) |
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) |