2020 - Fellow of the American Academy of Arts and Sciences
2019 - Fellow of the American Chemical Society
2017 - Fellow of John Simon Guggenheim Memorial Foundation
2009 - Fellow of Alfred P. Sloan Foundation
2008 - Hellman Fellow
His scientific interests lie mostly in Organic chemistry, Total synthesis, Catalysis, Combinatorial chemistry and Stereochemistry. Richmond Sarpong combines subjects such as Annulation and Organic synthesis with his study of Total synthesis. His Cycloisomerization study, which is part of a larger body of work in Catalysis, is frequently linked to Overall efficiency, bridging the gap between disciplines.
His research in Combinatorial chemistry intersects with topics in Natural product and Ring. Richmond Sarpong has researched Stereochemistry in several fields, including Guanidine and Dragmacidin D. His Stereoisomerism research incorporates elements of Bicyclic molecule and Cyclopropanation.
His primary areas of study are Stereochemistry, Organic chemistry, Catalysis, Total synthesis and Combinatorial chemistry. His Stereochemistry study frequently involves adjacent topics like Molecule. His research brings together the fields of Lycopodium and Organic chemistry.
Richmond Sarpong frequently studies issues relating to Pyridine and Catalysis. His work on Lycopodium alkaloid as part of general Total synthesis study is frequently connected to Chemical synthesis, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. Combinatorial chemistry and Amination are frequently intertwined in his study.
His primary areas of study are Stereochemistry, Total synthesis, Cleavage, Organic chemistry and Combinatorial chemistry. His Stereochemistry study frequently draws connections between adjacent fields such as Molecule. The various areas that Richmond Sarpong examines in his Total synthesis study include Calyciphylline B, Daphniphyllum, Chemical network, Ring and Natural product.
The study incorporates disciplines such as Bond cleavage, Catalysis, Ligand, Structural motif and Piperidine in addition to Cleavage. The Combinatorial chemistry study combines topics in areas such as Indane and Formal synthesis. Richmond Sarpong studied Bicyclic molecule and Intramolecular force that intersect with Drug discovery, Density functional theory and Amination.
Richmond Sarpong focuses on Stereochemistry, Total synthesis, Cleavage, Severe acute respiratory syndrome coronavirus 2 and 2019-20 coronavirus outbreak. He is interested in Piperidine, which is a field of Stereochemistry. His Total synthesis research includes themes of Natural product, Chemical network and Calyciphylline B, Daphniphyllum.
His Natural product research is multidisciplinary, incorporating elements of Indole test, Alkylation, Ring and Nicholas reaction. His Cleavage research is multidisciplinary, incorporating perspectives in Lactam, Bond cleavage, Catalysis, Transition metal and Reactivity. The study incorporates disciplines such as Single bond and Structural motif in addition to Catalysis.
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Production of the antimalarial drug precursor artemisinic acid in engineered yeast
Dae-Kyun Ro;Eric M. Paradise;Mario Ouellet;Karl J. Fisher.
Intramolecular C(sp3)–H amination
Jenna L. Jeffrey;Richmond Sarpong.
Chemical Science (2013)
The First Total Synthesis of Dragmacidin D
Neil K. Garg;Richmond Sarpong;Brian M. Stoltz.
Journal of the American Chemical Society (2002)
Application of in situ-generated Rh-bound trimethylenemethane variants to the synthesis of 3,4-fused pyrroles.
Erica E. Schultz;Richmond Sarpong.
Journal of the American Chemical Society (2013)
Total synthesis of (+)-complanadine A using an iridium-catalyzed pyridine C-H functionalization.
Daniel F. Fischer;Richmond Sarpong.
Journal of the American Chemical Society (2010)
Neonicotinoid insecticides induce salicylate-associated plant defense responses.
Kevin A. Ford;John E. Casida;Divya Chandran;Alexander G. Gulevich.
Proceedings of the National Academy of Sciences of the United States of America (2010)
Pt-Catalyzed Cyclization/1,2-Migration for the Synthesis of Indolizines, Pyrrolones, and Indolizinones
Cameron R. Smith;Eric M. Bunnelle;and Allison J. Rhodes;Richmond Sarpong.
Organic Letters (2007)
Toward a Symphony of Reactivity: Cascades Involving Catalysis and Sigmatropic Rearrangements
Amanda C. Jones;Jeremy A. May;Richmond Sarpong;Brian M. Stoltz.
Angewandte Chemie (2014)
Pt-catalyzed pentannulations from in situ generated metallo-carbenoids utilizing propargylic esters.
B. A. Bhanu Prasad;Francis K. Yoshimoto;Richmond Sarpong.
Journal of the American Chemical Society (2005)
Expedient Synthesis of Fused Azepine Derivatives Using a Sequential Rhodium(II)-Catalyzed Cyclopropanation/1-Aza-Cope Rearrangement of Dienyltriazoles
Erica E. Schultz;Vincent N. G. Lindsay;Richmond Sarpong.
Angewandte Chemie (2014)
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