Year |
Citation |
Score |
2023 |
Mao R, Wackelin DJ, Jamieson CS, Rogge T, Gao S, Das A, Taylor DM, Houk KN, Arnold FH. Enantio- and Diastereoenriched Enzymatic Synthesis of 1,2,3-Polysubstituted Cyclopropanes from (/)-Trisubstituted Enol Acetates. Journal of the American Chemical Society. PMID 37433085 DOI: 10.1021/jacs.3c04870 |
0.414 |
|
2023 |
Liu J, Lu J, Zhang C, Zhou Q, Jamieson CS, Shang C, Houk KN, Zhou J, Hu Y. Tandem intermolecular [4 + 2] cycloadditions are catalysed by glycosylated enzymes for natural product biosynthesis. Nature Chemistry. PMID 37365335 DOI: 10.1038/s41557-023-01260-8 |
0.348 |
|
2023 |
Niwa K, Ohashi M, Xie K, Chiang CY, Jamieson CS, Sato M, Watanabe K, Liu F, Houk KN, Tang Y. Biosynthesis of Polycyclic Natural Products from Conjugated Polyenes via Tandem Isomerization and Pericyclic Reactions. Journal of the American Chemical Society. 145: 13520-13525. PMID 37310230 DOI: 10.1021/jacs.3c02380 |
0.59 |
|
2023 |
Mao R, Wackelin DJ, Jamieson CS, Rogge T, Gao S, Das A, Taylor DM, Houk KN, Arnold FH. Enantio- and Diastereoenriched Enzymatic Synthesis of 1,2,3-Polysubstituted Cyclopropanes from (Z/E)-Trisubstituted Enol Acetates. Research Square. PMID 37090661 DOI: 10.21203/rs.3.rs-2802333/v1 |
0.747 |
|
2023 |
Jamieson CS, Sengupta A, Houk KN. Correction to "Cycloadditions of Cyclopentadiene and Cycloheptatriene with Tropones: All -[6+4] Cycloadditions Are Ambimodal". Journal of the American Chemical Society. PMID 37058599 DOI: 10.1021/jacs.3c03280 |
0.662 |
|
2023 |
Martin-Somer A, Xue XS, Jamieson CS, Zou Y, Houk KN. 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. PMID 36757329 DOI: 10.1021/jacs.2c12871 |
0.692 |
|
2023 |
Ohashi M, Tan D, Lu J, Jamieson CS, Kanayama D, Zhou J, Houk KN, Tang Y. Enzymatic Decalin Formation in Natural Product Biosynthesis. Journal of the American Chemical Society. PMID 36723171 DOI: 10.1021/jacs.2c12854 |
0.53 |
|
2022 |
Sun Z, Jamieson CS, Ohashi M, Houk KN, Tang Y. Discovery and characterization of a terpene biosynthetic pathway featuring a norbornene-forming Diels-Alderase. Nature Communications. 13: 2568. PMID 35546152 DOI: 10.1038/s41467-022-30288-6 |
0.575 |
|
2022 |
Jamieson CS, Ohashi M, Houk KN, Tang Y. Computational Prediction and Experimental Validation of a Bridged Cation Intermediate in Akanthomycin Biosynthesis. Journal of the American Chemical Society. 144: 5280-5283. PMID 35297629 DOI: 10.1021/jacs.2c02288 |
0.469 |
|
2021 |
Sato M, Kishimoto S, Yokoyama M, Jamieson CS, Narita K, Maeda N, Hara K, Hashimoto H, Tsunematsu Y, Houk KN, Tang Y, Watanabe K. Catalytic mechanism and -to- selectivity reversion of an octalin-forming natural Diels-Alderase. Nature Catalysis. 4: 223-232. PMID 35873532 DOI: 10.1038/s41929-021-00577-2 |
0.624 |
|
2021 |
Houk KN, Zhang H, Thøgersen MK, Jamieson CS, Xue XS, Jørgensen KA. Ambimodal Transition States in Diels-Alder Cycloadditions of Tropolone and Tropolonate with N-Methylmaleimide. Angewandte Chemie (International Ed. in English). PMID 34472178 DOI: 10.1002/anie.202109608 |
0.572 |
|
2021 |
Wang RB, Ma SG, Jamieson CS, Gao RM, Liu YB, Li Y, Wang XJ, Li YH, Houk KN, Qu J, Yu SS. Library construction of stereochemically diverse isomers of spirooliganin: their total synthesis and antiviral activity. Chemical Science. 12: 7003-7011. PMID 34123328 DOI: 10.1039/d1sc01277k |
0.497 |
|
2021 |
Bullock CX, Jamieson CS, Moënne-Loccoz P, Taylor B, Gonzalez JAM, Draves EA, Kuo LY. Sulfide Oxidation by 2,6-Bis[hydroxyl(methyl)amino]-4-morpholino-1,3,5-triazinatodioxomolybdenum(VI): Mechanistic Implications with DFT Calculations for a New Class of Molybdenum(VI) Complex. Inorganic Chemistry. PMID 33983027 DOI: 10.1021/acs.inorgchem.1c00145 |
0.526 |
|
2021 |
Jamieson CS, Misa J, Tang Y, Billingsley JM. Biosynthesis and synthetic biology of psychoactive natural products. Chemical Society Reviews. PMID 33908526 DOI: 10.1039/d1cs00065a |
0.444 |
|
2021 |
Zhang H, Novak AJE, Jamieson CS, Xue XS, Chen S, Trauner D, Houk KN. Computational Exploration of the Mechanism of Critical Steps in the Biomimetic Synthesis of Preuisolactone A, and Discovery of New Ambimodal (5 + 2)/(4 + 2) Cycloadditions. Journal of the American Chemical Society. PMID 33887906 DOI: 10.1021/jacs.1c01856 |
0.362 |
|
2021 |
Ohashi M, Kakule TB, Tang MC, Jamieson CS, Liu M, Zhao YL, Houk KN, Tang Y. Biosynthesis of Cyclophane-Containing Hirsutellone Family of Fungal Natural Products. Journal of the American Chemical Society. PMID 33834778 DOI: 10.1021/jacs.1c00098 |
0.506 |
|
2021 |
Jamieson CS, Sengupta A, Houk KN. Cycloadditions of Cyclopentadiene and Cycloheptatriene with Tropones: All -[6+4] Cycloadditions Are Ambimodal. Journal of the American Chemical Society. PMID 33656318 DOI: 10.1021/jacs.0c13401 |
0.751 |
|
2021 |
Einsiedler M, Jamieson CS, Maskeri M, Houk KN, Gulder TAM. Fungal Dioxygenase AsqJ Is Promiscuous and Bimodal: Substrate-Directed Formation of Quinolones versus Quinazolinones. Angewandte Chemie (International Ed. in English). PMID 33411393 DOI: 10.1002/anie.202017086 |
0.724 |
|
2020 |
Yan Y, Zang X, Jamieson CS, Lin HC, Houk KN, Zhou J, Tang Y. Biosynthesis of the fungal glyceraldehyde-3-phosphate dehydrogenase inhibitor heptelidic acid and mechanism of self-resistance. Chemical Science. 11: 9554-9562. PMID 34094220 DOI: 10.1039/d0sc03805a |
0.335 |
|
2020 |
Gao DW, Jamieson CS, Wang G, Yan Y, Zhou J, Houk KN, Tang Y. A Polyketide Cyclase That Forms Medium-Ring Lactones. Journal of the American Chemical Society. PMID 33351624 DOI: 10.1021/jacs.0c11226 |
0.716 |
|
2020 |
Ohashi M, Jamieson CS, Cai Y, Tan D, Kanayama D, Tang MC, Anthony SM, Chari JV, Barber JS, Picazo E, Kakule TB, Cao S, Garg NK, Zhou J, Houk KN, et al. An enzymatic Alder-ene reaction. Nature. 586: 64-69. PMID 32999480 DOI: 10.1038/s41586-020-2743-5 |
0.549 |
|
2020 |
Yan Y, Zang X, Jamieson CS, Lin H, Houk KN, Zhou J, Tang Y. Biosynthesis of the fungal glyceraldehyde-3-phosphate dehydrogenase inhibitor heptelidic acid and mechanism of self-resistance Chemical Science. 11: 9554-9562. DOI: 10.1039/D0Sc03805A |
0.379 |
|
2019 |
McLeod D, Thøgersen MK, Jessen NI, Jørgensen KA, Jamieson CS, Xue XS, Houk KN, Liu F, Hoffmann R. Expanding the Frontiers of Higher-Order Cycloadditions. Accounts of Chemical Research. PMID 31789016 DOI: 10.1021/Acs.Accounts.9B00498 |
0.654 |
|
2019 |
Quintela-Varela H, Jamieson C, Shao Q, Houk K, Trauner D. Bioinspired Synthesis of (-)-PF-1018. Angewandte Chemie (International Ed. in English). PMID 31788926 DOI: 10.1002/Anie.201912452 |
0.541 |
|
2019 |
Chen Q, Gao J, Jamieson C, Liu J, Ohashi M, Bai J, Yan D, Liu B, Che Y, Wang Y, Houk KN, Hu Y. Enzymatic Intermolecular Hetero-Diels-Alder Reaction in the Biosynthesis of Tropolonic Sesquiterpenes. Journal of the American Chemical Society. PMID 31461283 DOI: 10.1021/Jacs.9B06592 |
0.616 |
|
2019 |
Cai Y, Hai Y, Ohashi M, Jamieson CS, Garcia-Borras M, Houk KN, Zhou J, Tang Y. Structural basis for stereoselective dehydration and hydrogen-bonding catalysis by the SAM-dependent pericyclase LepI. Nature Chemistry. PMID 31332284 DOI: 10.2210/Pdb6Ix9/Pdb |
0.747 |
|
2019 |
Zhang Z, Jamieson CS, Zhao YL, Li D, Ohashi M, Houk KN, Tang Y. Enzyme-catalyzed inverse-electron demand Diels-Alder reaction in the biosynthesis of antifungal ilicicolin H. Journal of the American Chemical Society. PMID 30905148 DOI: 10.1021/Jacs.9B02204 |
0.63 |
|
2019 |
Xue XS, Jamieson CS, Garcia-Borràs M, Dong X, Yang Z, Houk KN. An Ambimodal Trispericyclic Transition State and Dynamic Control of Periselectivity. Journal of the American Chemical Society. PMID 30623652 DOI: 10.1021/Jacs.8B12674 |
0.766 |
|
2019 |
Tan D, Jamieson CS, Ohashi M, Tang MC, Houk KN, Tang Y. Genome-mined Diels-Alderase catalyzes formation of the cis-octahydrodecalins of varicidin A and B. Journal of the American Chemical Society. PMID 30609896 DOI: 10.1021/Jacs.8B12010 |
0.618 |
|
2019 |
Yang Z, Jamieson CS, Xue X, Garcia-Borràs M, Benton T, Dong X, Liu F, Houk K. Mechanisms and Dynamics of Reactions Involving Entropic Intermediates Trends in Chemistry. 1: 22-34. DOI: 10.1016/j.trechm.2019.01.009 |
0.705 |
|
2018 |
Jamieson CS, Ohashi M, Liu F, Tang Y, Houk KN. The expanding world of biosynthetic pericyclases: cooperation of experiment and theory for discovery. Natural Product Reports. PMID 30311924 DOI: 10.1039/C8Np00075A |
0.667 |
|
2018 |
Yang Z, Dong X, Yu Y, Yu P, Li Y, Jamieson C, Houk KN. Relationships Between Product Ratios in Ambimodal Pericyclic Reactions and Bond Lengths in Transition Structures. Journal of the American Chemical Society. PMID 29419295 DOI: 10.1021/Jacs.7B13562 |
0.73 |
|
2018 |
Kreiman HW, Batali ME, Jamieson C, Lyon MA, Duncan JA. CASSCF Calculations Reveal Competitive Chair (Pericyclic) and Boat (Pseudopericyclic) Transition States for the [3,3] Sigmatropic Rearrangement of Allyl Esters. The Journal of Organic Chemistry. PMID 29350923 DOI: 10.1021/Acs.Joc.7B02316 |
0.386 |
|
Low-probability matches (unlikely to be authored by this person) |
2021 |
Bemis CY, Ungarean CN, Shved AS, Jamieson CS, Hwang T, Lee KS, Houk KN, Sarlah D. Total Synthesis and Computational Investigations of Sesquiterpene-Tropolones Ameliorate Stereochemical Inconsistencies and Resolve an Ambiguous Biosynthetic Relationship. Journal of the American Chemical Society. PMID 33825475 DOI: 10.1021/jacs.1c02150 |
0.274 |
|
Hide low-probability matches. |