| Year |
Citation |
Score |
| 2021 |
León Rayo DF, Hong YJ, Campeau D, Tantillo DJ, Gagosz F. On the Mechanism of Au-catalyzed Enynamide-Yne Dehydro-Diels-Alder Reactions: An Experimental and Computational Study. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33945650 DOI: 10.1002/chem.202100580 |
0.478 |
|
| 2018 |
Pelot KA, Hagelthorn DM, Hong YJ, Tantillo DJ, Zerbe P. Diterpene Synthase-Catalyzed Biosynthesis of Distinct Clerodane Stereoisomers. Chembiochem : a European Journal of Chemical Biology. PMID 30393911 DOI: 10.1002/Cbic.201800580 |
0.419 |
|
| 2018 |
Hong YJ, Tantillo DJ. A Maze of Dyotropic Rearrangements and Triple Shifts: Carbocation Rearrangements Connecting Stemarene, Stemodene, Betaerdene, Aphidicolene and Scopadulanol. The Journal of Organic Chemistry. PMID 29494166 DOI: 10.1021/Acs.Joc.8B00138 |
0.485 |
|
| 2018 |
Xu M, Jia M, Hong YJ, Yin X, Tantillo DJ, Proteau PJ, Peters RJ. Premutilin Synthase: Ring Rearrangement by a Class II Diterpene Cyclase. Organic Letters. PMID 29388775 DOI: 10.1021/Acs.Orglett.8B00121 |
0.452 |
|
| 2017 |
Bartels F, Hong YJ, Ueda D, Weber M, Sato T, Tantillo DJ, Christmann M. Bioinspired synthesis of pentacyclic onocerane triterpenoids. Chemical Science. 8: 8285-8290. PMID 29619174 DOI: 10.1039/C7Sc03903D |
0.435 |
|
| 2017 |
Christmann M, Schmiedel VM, Hong YJ, Lentz D, Tantillo D. Synthesis and Structure Revision of Dichrocephones A and B. Angewandte Chemie (International Ed. in English). PMID 29251825 DOI: 10.1002/Anie.201711766 |
0.455 |
|
| 2017 |
Huang AC, Hong YJ, Bond AD, Tantillo DJ, Osbourn A. Diverged Plant Terpene Synthases Reroute the Carbocation Cyclization Path towards the Formation of Unprecedented 6/11/5 and 6/6/7/5 Sesterterpene Scaffolds. Angewandte Chemie (International Ed. in English). PMID 29194888 DOI: 10.1002/Anie.201711444 |
0.487 |
|
| 2017 |
Xu Y, Hong YJ, Tantillo DJ, Brown MK. Intramolecular Chirality Transfer [2 + 2] Cycloadditions of Allenoates and Alkenes. Organic Letters. PMID 28686031 DOI: 10.1021/Acs.Orglett.7B01420 |
0.384 |
|
| 2017 |
Huang AC, Kautsar SA, Hong YJ, Medema MH, Bond AD, Tantillo DJ, Osbourn A. Unearthing a sesterterpene biosynthetic repertoire in the Brassicaceae through genome mining reveals convergent evolution. Proceedings of the National Academy of Sciences of the United States of America. PMID 28673978 DOI: 10.1073/Pnas.1705567114 |
0.429 |
|
| 2017 |
Hong YJ, Tantillo DJ. Is a 1,4-Alkyl Shift Involved in the Biosynthesis of Ledol and Viridiflorol? The Journal of Organic Chemistry. PMID 28277661 DOI: 10.1021/Acs.Joc.7B00187 |
0.465 |
|
| 2017 |
Hong YJ, Tantillo DJ. The Variediene-Forming Carbocation Cyclization/Rearrangement Cascade Australian Journal of Chemistry. 70: 362. DOI: 10.1071/Ch16504 |
0.441 |
|
| 2016 |
Potter KC, Jia M, Hong YJ, Tantillo D, Peters RJ. Product Rearrangement from Altering a Single Residue in the Rice syn-Copalyl Diphosphate Synthase. Organic Letters. PMID 26878189 DOI: 10.1021/Acs.Orglett.6B00181 |
0.497 |
|
| 2015 |
Potter KC, Zi J, Hong YJ, Schulte S, Malchow B, Tantillo DJ, Peters RJ. Blocking Deprotonation with Retention of Aromaticity in a Plant ent-Copalyl Diphosphate Synthase Leads to Product Rearrangement. Angewandte Chemie (International Ed. in English). PMID 26603275 DOI: 10.1002/Anie.201509060 |
0.493 |
|
| 2015 |
Hong YJ, Tantillo DJ. Correction: The energetic viability of an unexpected skeletal rearrangement in cyclooctatin biosynthesis. Organic & Biomolecular Chemistry. 13: 11140. PMID 26526514 DOI: 10.1039/C5Ob90181B |
0.403 |
|
| 2015 |
Hong YJ, Tantillo DJ. Tension between Internal and External Modes of Stabilization in Carbocations Relevant to Terpene Biosynthesis: Modulating Minima Depth via C-H···π Interactions. Organic Letters. PMID 26506248 DOI: 10.1021/Acs.Orglett.5B02740 |
0.439 |
|
| 2015 |
Hong YJ, Tantillo DJ. The energetic viability of an unexpected skeletal rearrangement in cyclooctatin biosynthesis. Organic & Biomolecular Chemistry. PMID 26371548 DOI: 10.1039/C5Ob01785H |
0.454 |
|
| 2015 |
Hong YJ, Tantillo DJ. Feasibility of intramolecular proton transfers in terpene biosynthesis--guiding principles. Journal of the American Chemical Society. 137: 4134-40. PMID 25764274 DOI: 10.1021/Ja512685X |
0.485 |
|
| 2015 |
Hong YJ, Giner JL, Tantillo DJ. Bicyclobutonium ions in biosynthesis--interconversion of cyclopropyl-containing sterols from orchids. Journal of the American Chemical Society. 137: 2085-8. PMID 25607948 DOI: 10.1021/Ja512901A |
0.378 |
|
| 2014 |
Zi J, Matsuba Y, Hong YJ, Jackson AJ, Tantillo DJ, Pichersky E, Peters RJ. Biosynthesis of lycosantalonol, a cis-prenyl derived diterpenoid. Journal of the American Chemical Society. 136: 16951-3. PMID 25406026 DOI: 10.1021/Ja508477E |
0.497 |
|
| 2014 |
Rasik CM, Hong YJ, Tantillo DJ, Brown MK. Origins of diastereoselectivity in Lewis acid promoted ketene-alkene [2 + 2] cycloadditions. Organic Letters. 16: 5168-71. PMID 25230201 DOI: 10.1021/Ol5025184 |
0.405 |
|
| 2014 |
Hong YJ, Tantillo DJ. How cyclobutanes are assembled in nature--insights from quantum chemistry. Chemical Society Reviews. 43: 5042-50. PMID 24710596 DOI: 10.1039/C3Cs60452G |
0.48 |
|
| 2014 |
Hong YJ, Tantillo DJ. Branching out from the bisabolyl cation. Unifying mechanistic pathways to barbatene, bazzanene, chamigrene, chamipinene, cumacrene, cuprenene, dunniene, isobazzanene, iso-γ-bisabolene, isochamigrene, laurene, microbiotene, sesquithujene, sesquisabinene, thujopsene, trichodiene, and widdradiene sesquiterpenes. Journal of the American Chemical Society. 136: 2450-63. PMID 24490652 DOI: 10.1021/Ja4106489 |
0.5 |
|
| 2014 |
Hong YJ, Tantillo DJ. Biosynthetic consequences of multiple sequential post-transition-state bifurcations. Nature Chemistry. 6: 104-11. PMID 24451585 DOI: 10.1038/Nchem.1843 |
0.483 |
|
| 2014 |
Hong YJ, Tantillo DJ. Viability of nonclassical carbocations proposed as intermediates in the biosynthesis of atiserene, beyerene, kaurene, and trachylobane diterpenes Helvetica Chimica Acta. 97: 1475-1480. DOI: 10.1002/Hlca.201400082 |
0.469 |
|
| 2013 |
Chooi YH, Hong YJ, Cacho RA, Tantillo DJ, Tang Y. A cytochrome P450 serves as an unexpected terpene cyclase during fungal meroterpenoid biosynthesis. Journal of the American Chemical Society. 135: 16805-8. PMID 24161266 DOI: 10.1021/Ja408966T |
0.482 |
|
| 2013 |
Hong YJ, Irmisch S, Wang SC, Garms S, Gershenzon J, Zu L, Köllner TG, Tantillo DJ. Theoretical and experimental analysis of the reaction mechanism of MrTPS2, a triquinane-forming sesquiterpene synthase from chamomile. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13590-600. PMID 23963956 DOI: 10.1002/Chem.201301018 |
0.502 |
|
| 2013 |
Vaughan MM, Wang Q, Webster FX, Kiemle D, Hong YJ, Tantillo DJ, Coates RM, Wray AT, Askew W, O'Donnell C, Tokuhisa JG, Tholl D. Formation of the unusual semivolatile diterpene rhizathalene by the Arabidopsis class I terpene synthase TPS08 in the root stele is involved in defense against belowground herbivory. The Plant Cell. 25: 1108-25. PMID 23512856 DOI: 10.1105/Tpc.112.100057 |
0.418 |
|
| 2013 |
Hong YJ, Giner JL, Tantillo DJ. Triple shifts and thioether assistance in rearrangements associated with an unusual biomethylation of the sterol side chain. The Journal of Organic Chemistry. 78: 935-41. PMID 23270431 DOI: 10.1021/Jo3024208 |
0.508 |
|
| 2013 |
Pemberton RP, Hong YJ, Tantillo DJ. Inherent dynamical preferences in carbocation rearrangements leading to terpene natural products Pure and Applied Chemistry. 85: 1949-1957. DOI: 10.1351/Pac-Con-12-11-22 |
0.435 |
|
| 2013 |
Hong YJ, Tantillo DJ. C-H⋯π interactions as modulators of carbocation structure-implications for terpene biosynthesis Chemical Science. 4: 2512-2518. DOI: 10.1039/C3Sc50571E |
0.437 |
|
| 2012 |
Hong YJ, Ponec R, Tantillo DJ. Changes in charge distribution, molecular volume, accessible surface area and electronic structure along the reaction coordinate for a carbocationic triple shift rearrangement of relevance to diterpene biosynthesis. The Journal of Physical Chemistry. A. 116: 8902-9. PMID 22881994 DOI: 10.1021/Jp3047328 |
0.458 |
|
| 2012 |
Hong YJ, Tantillo DJ. Theoretical calculations on carbocations involved in the biosynthesis of bergamotenes and related terpenes--the same and not the same. Chemical Communications (Cambridge, England). 48: 1571-3. PMID 21983931 DOI: 10.1039/C1Cc14414F |
0.457 |
|
| 2011 |
Hong YJ, Tantillo DJ. The taxadiene-forming carbocation cascade. Journal of the American Chemical Society. 133: 18249-56. PMID 21988104 DOI: 10.1021/Ja2055929 |
0.493 |
|
| 2011 |
Hong YJ, Tantillo DJ. How many secondary carbocations are involved in the biosynthesis of avermitilol? Organic Letters. 13: 1294-7. PMID 21322615 DOI: 10.1021/Ol103079V |
0.483 |
|
| 2011 |
Hong YJ, Tantillo DJ. Does gold as a substituent accelerate [3,3] sigmatropic shifts? Organometallics. 30: 5825-5831. DOI: 10.1021/Om200676N |
0.39 |
|
| 2010 |
Hong YJ, Tantillo DJ. Quantum chemical dissection of the classic terpinyl/pinyl/bornyl/camphyl cation conundrum-the role of pyrophosphate in manipulating pathways to monoterpenes. Organic & Biomolecular Chemistry. 8: 4589-600. PMID 20725661 DOI: 10.1039/C0Ob00167H |
0.491 |
|
| 2010 |
Hong YJ, Tantillo DJ. Formation of beyerene, kaurene, trachylobane, and atiserene diterpenes by rearrangements that avoid secondary carbocations. Journal of the American Chemical Society. 132: 5375-86. PMID 20353180 DOI: 10.1021/Ja9084786 |
0.492 |
|
| 2010 |
Hong YJ, Tantillo DJ. A tangled web-interconnecting pathways to amorphadiene and the amorphene sesquiterpenes Chemical Science. 1: 609-614. DOI: 10.1039/C0Sc00333F |
0.502 |
|
| 2009 |
Hong YJ, Tantillo DJ. A potential energy surface bifurcation in terpene biosynthesis. Nature Chemistry. 1: 384-9. PMID 21378892 DOI: 10.1038/Nchem.287 |
0.46 |
|
| 2009 |
Hong YJ, Tantillo DJ. Modes of inactivation of trichodiene synthase by a cyclopropane-containing farnesyldiphosphate analog. Organic & Biomolecular Chemistry. 7: 4101-9. PMID 19763318 DOI: 10.1039/B908738A |
0.493 |
|
| 2009 |
Hong YJ, Tantillo DJ. Consequences of conformational preorganization in sesquiterpene biosynthesis: theoretical studies on the formation of the bisabolene, curcumene, acoradiene, zizaene, cedrene, duprezianene, and sesquithuriferol sesquiterpenes. Journal of the American Chemical Society. 131: 7999-8015. PMID 19469543 DOI: 10.1021/Ja9005332 |
0.481 |
|
| 2007 |
Hong YJ, Tantillo DJ. Perturbing the structure of the 2-norbornyl cation through C-H...N and C-H...pi interactions. The Journal of Organic Chemistry. 72: 8877-81. PMID 17941673 DOI: 10.1021/Jo701526X |
0.489 |
|
| 2006 |
Hong YJ, Tantillo DJ. Which is more likely in trichodiene biosynthesis: hydride or proton transfer? Organic Letters. 8: 4601-4. PMID 16986960 DOI: 10.1021/Ol061884F |
0.464 |
|
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