Cooper Stergis Jamieson
Affiliations: | University of California, Los Angeles, Los Angeles, CA |
Area:
Pericyclases, ambimodal reactions, natural product biosynthesis, computational chemistryWebsite:
https://www.researchgate.net/profile/Cooper_JamiesonGoogle:
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Publications
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| Mao R, Wackelin DJ, Jamieson CS, et al. (2023) Enantio- and Diastereoenriched Enzymatic Synthesis of 1,2,3-Polysubstituted Cyclopropanes from (/)-Trisubstituted Enol Acetates. Journal of the American Chemical Society |
| Liu J, Lu J, Zhang C, et al. (2023) Tandem intermolecular [4 + 2] cycloadditions are catalysed by glycosylated enzymes for natural product biosynthesis. Nature Chemistry |
| Niwa K, Ohashi M, Xie K, et al. (2023) Biosynthesis of Polycyclic Natural Products from Conjugated Polyenes via Tandem Isomerization and Pericyclic Reactions. Journal of the American Chemical Society. 145: 13520-13525 |
| Mao R, Wackelin DJ, Jamieson CS, et al. (2023) Enantio- and Diastereoenriched Enzymatic Synthesis of 1,2,3-Polysubstituted Cyclopropanes from (Z/E)-Trisubstituted Enol Acetates. Research Square |
| Jamieson CS, Sengupta A, Houk KN. (2023) Correction to "Cycloadditions of Cyclopentadiene and Cycloheptatriene with Tropones: All -[6+4] Cycloadditions Are Ambimodal". Journal of the American Chemical Society |
| Martin-Somer A, Xue XS, Jamieson CS, et al. (2023) Computational Design of a Tetrapericyclic Cycloaddition and the Nature of Potential Energy Surfaces with Multiple Bifurcations. Journal of the American Chemical Society. 145: 4221-30 |
| Ohashi M, Tan D, Lu J, et al. (2023) Enzymatic Decalin Formation in Natural Product Biosynthesis. Journal of the American Chemical Society |
| Sun Z, Jamieson CS, Ohashi M, et al. (2022) Discovery and characterization of a terpene biosynthetic pathway featuring a norbornene-forming Diels-Alderase. Nature Communications. 13: 2568 |
| Jamieson CS, Ohashi M, Houk KN, et al. (2022) Computational Prediction and Experimental Validation of a Bridged Cation Intermediate in Akanthomycin Biosynthesis. Journal of the American Chemical Society. 144: 5280-5283 |
| Sato M, Kishimoto S, Yokoyama M, et al. (2021) Catalytic mechanism and -to- selectivity reversion of an octalin-forming natural Diels-Alderase. Nature Catalysis. 4: 223-232 |