| Year |
Citation |
Score |
| 2023 |
Guo LD, Wu Y, Xu X, Lin Z, Tong R. Bent π-Conjugation within a Macrocycle: Asymmetric Total Syntheses of Spirohexenolides A and B. Angewandte Chemie (International Ed. in English). e202316259. PMID 37988261 DOI: 10.1002/anie.202316259 |
0.459 |
|
| 2023 |
Cheng WF, Ma S, Lai YT, Cheung YT, Akkarasereenon K, Zhou Y, Tong R. BiBr3-Mediated Intramolecular Aza-Prins Cyclization of Aza-Achmatowicz Rearrangement Products: Asymmetric Total Synthesis of Suaveoline and Sarpagine Alkaloids. Angewandte Chemie (International Ed. in English). e202311671. PMID 37724977 DOI: 10.1002/anie.202311671 |
0.521 |
|
| 2023 |
Wei W, Cheung KK, Lin R, Kong LC, Chan KL, Sung HHY, Williams ID, Tong R, Lin Z, Jia G. [2+2+1+1] Cycloaddition for de novo Synthesis of Densely Functionalized Phenols. Angewandte Chemie (International Ed. in English). e202307251. PMID 37428447 DOI: 10.1002/anie.202307251 |
0.396 |
|
| 2022 |
Tian P, Ye W, Zhang X, Tong Y, Qian PY, Tong R. Ten-step asymmetric total syntheses of potent antibiotics anthracimycin and anthracimycin B. Chemical Science. 13: 12776-12781. PMID 36519065 DOI: 10.1039/d2sc05049h |
0.394 |
|
| 2022 |
Liang L, Guo LD, Tong R. Achmatowicz Rearrangement-Inspired Development of Green Chemistry, Organic Methodology, and Total Synthesis of Natural Products. Accounts of Chemical Research. 55: 2326-2340. PMID 35916456 DOI: 10.1021/acs.accounts.2c00358 |
0.41 |
|
| 2022 |
Zhang X, Tong Y, Li G, Zhao H, Chen G, Yao H, Tong R. 1,5-Allyl Shift by a Sequential Achmatowicz/Oxonia-Cope/Retro-Achmatowicz Rearrangement. Angewandte Chemie (International Ed. in English). PMID 35670657 DOI: 10.1002/anie.202205919 |
0.368 |
|
| 2021 |
Guo L, Xu Z, Tong R. Asymmetric Total Synthesis of Indole Diterpenes Paspalicine, Paspalinine, and Paspalinine-13-ene. Angewandte Chemie (International Ed. in English). PMID 34784090 DOI: 10.1002/anie.202115384 |
0.452 |
|
| 2021 |
Márquez-Cadena MA, Zhang W, Tong R. Synthetic Studies toward the Berkeleyacetal Core Architecture. Organic Letters. 23: 9227-9231. PMID 34780201 DOI: 10.1021/acs.orglett.1c03559 |
0.369 |
|
| 2021 |
Liang L, Zhou S, Zhang W, Tong R. Catalytic Asymmetric Alkynylation of 3,4-Dihydro-β-carbolinium Ions Enables Collective Total Syntheses of Indole Alkaloids. Angewandte Chemie (International Ed. in English). PMID 34581483 DOI: 10.1002/anie.202112383 |
0.308 |
|
| 2020 |
Wang J, Márquez-Cadena MA, Tong R. Asymmetric Total Syntheses of (+)-Penostatins A and C. Organic Letters. PMID 32543859 DOI: 10.1021/Acs.Orglett.0C01649 |
0.443 |
|
| 2020 |
Liaw MW, Cheng WF, Tong R. C-Aryl Glycosylation: Palladium-catalyzed Aryl-Allyl Coupling of Achmatowicz Rearrangement Products with Arylboronic Acids. The Journal of Organic Chemistry. PMID 32314587 DOI: 10.1021/Acs.Joc.0C00688 |
0.415 |
|
| 2020 |
Song L, Su Q, Lin X, Du Z, Xu H, Ouyang MA, Yao H, Tong R. Cascade Claisen and Meinwald Rearrangement for One-Pot Divergent Synthesis of Benzofurans and 2-Chromenes. Organic Letters. PMID 32242416 DOI: 10.1021/Acs.Orglett.0C00770 |
0.588 |
|
| 2019 |
Zhao G, Canterbury DP, Taylor AP, Cheng X, Mikochik P, Bagley SW, Tong R. Synthesis of 2-Arylpiperidines via Pd-Catalyzed Arylation of Aza-Achmatowicz Rearrangement Products with Arylboronic Acids. Organic Letters. PMID 31880455 DOI: 10.1021/Acs.Orglett.9B04220 |
0.464 |
|
| 2019 |
Márquez-Cadena MA, Ren J, Ye W, Qian P, Tong R. Asymmetric Total Synthesis Enables Discovery of Antibacterial Activity of Siladenoserinols A and H. Organic Letters. PMID 31747295 DOI: 10.1021/Acs.Orglett.9B03857 |
0.319 |
|
| 2019 |
Xu J, Liang L, Zheng H, Chi YR, Tong R. Green oxidation of indoles using halide catalysis. Nature Communications. 10: 4754. PMID 31628334 DOI: 10.1038/S41467-019-12768-4 |
0.308 |
|
| 2019 |
Wang YC, Ma Y, Li X, Kuang BY, Huang C, Tong R, Yu JZ. Monoterpene and sesquiterpene α-hydroxy organosulfates: Synthesis, MS/MS characteristics, and ambient presence. Environmental Science & Technology. PMID 31584263 DOI: 10.1021/Acs.Est.9B04703 |
0.303 |
|
| 2019 |
Zhang Z, Zhang W, Kang F, Ip FCF, Ip NY, Tong R. Asymmetric Total Syntheses of Rhynchophylline and Isorhynchophylline. The Journal of Organic Chemistry. PMID 31416310 DOI: 10.1021/Acs.Joc.9B01977 |
0.507 |
|
| 2019 |
Zhao N, Xie S, Tian P, Tong R, Ning C, Xu J. Asymmetric total synthesis of (+)-astellatol and (−)-astellatene Organic Chemistry Frontiers. 6: 2014-2022. DOI: 10.1039/C9Qo00384C |
0.495 |
|
| 2019 |
Zhao G, Tong R. A solvent-free catalytic protocol for the Achmatowicz rearrangement Green Chemistry. 21: 64-68. DOI: 10.1039/C8Gc03030H |
0.327 |
|
| 2019 |
Zhao G, Tong R. Silica gel enables Achmatowicz rearrangement with KBr/oxone under “anhydrous” condition for one-pot functionalization Tetrahedron. 75: 1669-1675. DOI: 10.1016/J.Tet.2018.12.022 |
0.395 |
|
| 2018 |
Zhao G, Liang L, Wen CHE, Tong R. In Situ Generation of Nitrile Oxides from NaCl-Oxone Oxidation of Various Aldoximes and Their 1,3-Dipolar Cycloaddition. Organic Letters. PMID 30576159 DOI: 10.1021/Acs.Orglett.8B03829 |
0.347 |
|
| 2018 |
Yu J, Zhang Z, Zhou S, Zhang W, Tong R. Evolution of two routes for asymmetric total synthesis of tetrahydroprotoberberine alkaloids Organic Chemistry Frontiers. 5: 242-246. DOI: 10.1039/C7Qo00776K |
0.543 |
|
| 2017 |
Fu G, Zhang W, Du D, Ng YP, Ip FCF, Tong R, Ip NY. Diarylheptanoids from Rhizomes of Alpinia officinarum Inhibit Aggregation of Alpha-synuclein. Journal of Agricultural and Food Chemistry. PMID 28707886 DOI: 10.1021/Acs.Jafc.7B02021 |
0.368 |
|
| 2017 |
Cheng H, Zhang Z, Yao H, Zhang W, Yu J, Tong R. Unified Asymmetric Total Syntheses of Alotaketals A-D and Phorbaketal A. Angewandte Chemie (International Ed. in English). PMID 28574668 DOI: 10.1002/Anie.201704628 |
0.412 |
|
| 2017 |
Wang Y, Ren J, Huang XHH, Tong R, Yu JZ. Synthesis of Four Monoterpene-derived Organosulfates and their Quantification in Atmospheric Aerosol Samples. Environmental Science & Technology. PMID 28549212 DOI: 10.1021/Acs.Est.7B01179 |
0.334 |
|
| 2017 |
Song L, Huang F, Guo L, Ouyang MA, Tong R. A cascade Claisen rearrangement/o-quinone methide formation/electrocyclization approach to 2H-chromenes. Chemical Communications (Cambridge, England). PMID 28524196 DOI: 10.1039/C7Cc03037A |
0.425 |
|
| 2017 |
Zhang W, Yao H, Yu J, Zhang Z, Tong R. Total Syntheses of Sesterterpenoid Ansellones A and B, and Phorbadione. Angewandte Chemie (International Ed. in English). PMID 28371092 DOI: 10.1002/Anie.201701879 |
0.524 |
|
| 2017 |
Zhou S, Tong R. Three-Step Catalytic Asymmetric Total Syntheses of 13-Methyltetrahydroprotoberberine Alkaloids. Organic Letters. PMID 28346788 DOI: 10.1021/Acs.Orglett.7B00414 |
0.47 |
|
| 2017 |
Yao H, Wang J, Tong R. Recent Developments in Total Syntheses of Cephalosporolides, Penisporolides, and Ascospiroketals. Chemical Record (New York, N.Y.). PMID 28272766 DOI: 10.1002/Tcr.201700001 |
0.511 |
|
| 2017 |
Tong R, Zhang Z. Synthetic Approaches to 2,6-trans-Tetrahydropyrans Synthesis. 49: 4899-4916. DOI: 10.1055/S-0036-1588577 |
0.528 |
|
| 2017 |
Xu J, Tong R. An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives Green Chemistry. 19: 2952-2956. DOI: 10.1039/C7Gc01341H |
0.409 |
|
| 2017 |
Wang J, Tong R. A NMR method for relative stereochemical assignments of the tricyclic core of cephalosporolides, penisporolides and related synthetic analogues Organic Chemistry Frontiers. 4: 140-146. DOI: 10.1039/C6Qo00556J |
0.346 |
|
| 2016 |
Li Z, Tong R. Asymmetric Total Syntheses of (‒)-Hedycoropyrans A and B. The Journal of Organic Chemistry. PMID 28029045 DOI: 10.1021/Acs.Joc.6B02738 |
0.561 |
|
| 2016 |
Li H, Tong R, Sun J. Catalytic Enantioselective Aza-Piancatelli Rearrangement. Angewandte Chemie (International Ed. in English). PMID 27785871 DOI: 10.1002/Anie.201607714 |
0.428 |
|
| 2016 |
Yu J, Zhou Y, Lin Z, Tong R. Regioselective and Stereospecific Copper-Catalyzed Deoxygenation of Epoxides to Alkenes. Organic Letters. PMID 27596225 DOI: 10.1021/Acs.Orglett.6B02405 |
0.347 |
|
| 2016 |
Li Z, Tong R. A Catalytic Environment-friendly Protocol for Achmatowicz Rearrangement. The Journal of Organic Chemistry. PMID 27167167 DOI: 10.1021/Acs.Joc.6B00469 |
0.421 |
|
| 2016 |
Wang J, Tong R. Total Synthesis of Purported Cephalosporolides H and I, Penisporolide B, and Their Stereoisomers. The Journal of Organic Chemistry. PMID 27137949 DOI: 10.1021/Acs.Joc.6B00788 |
0.438 |
|
| 2016 |
Wang J, Tong R. Asymmetric Total Syntheses of ent-Ascospiroketals A and B. Organic Letters. PMID 27043130 DOI: 10.1021/Acs.Orglett.6B00796 |
0.577 |
|
| 2016 |
Tong R, Zhou S. A General Concise Strategy Enables Collective Total Syntheses of > 50 Protoberberine and 5 Aporhoeadane Alkaloids within 4-8 steps. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26990887 DOI: 10.1002/Chem.201601245 |
0.502 |
|
| 2016 |
Zhang W, Tong R. Synthetic Approaches to Construct the 6,8-DOBCO Framework in Natural Products. The Journal of Organic Chemistry. PMID 26954099 DOI: 10.1021/Acs.Joc.6B00246 |
0.474 |
|
| 2016 |
Li Z, Tong R. Asymmetric Total Syntheses of the trans -2-Aryl-6-alkyltetrahydropyrans Diospongin B and Parvistones D and e from a Common Precursor Synthesis (Germany). 48: 1630-1636. DOI: 10.1055/S-0035-1561592 |
0.447 |
|
| 2016 |
Yu J, Ma H, Yao H, Cheng H, Tong R. Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds Organic Chemistry Frontiers. 3: 714-719. DOI: 10.1039/C6Qo00034G |
0.445 |
|
| 2016 |
Song L, Yao H, Dai Y, Wu M, Tong R. Recent developments in total syntheses of aculeatins Tetrahedron Letters. 57: 4257-4263. DOI: 10.1016/J.Tetlet.2016.08.041 |
0.458 |
|
| 2016 |
Zhou S, Tong R. ChemInform Abstract: A General, Concise Strategy That Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps. Cheminform. 47. DOI: 10.1002/CHIN.201641220 |
0.332 |
|
| 2015 |
Zhu L, Tong R. Total synthesis of ent-(+)-cinanthrenol A. The Journal of Antibiotics. PMID 26555362 DOI: 10.1038/Ja.2015.114 |
0.541 |
|
| 2015 |
Li Z, Ip FC, Ip NY, Tong R. Highly trans-Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ-Deoxygenation and Heck-Matsuda Reaction: Asymmetric Total Synthesis of (-)-Musellarins A-C and Their Analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26104266 DOI: 10.1002/Chem.201501713 |
0.552 |
|
| 2015 |
Zhu L, Tong R. Structural revision of (+)-uprolide F diacetate confirmed by asymmetric total synthesis. Organic Letters. 17: 1966-9. PMID 25831074 DOI: 10.1021/Acs.Orglett.5B00700 |
0.498 |
|
| 2015 |
Ren J, Wang J, Tong R. Asymmetric total synthesis of (+)-attenol B. Organic Letters. 17: 744-7. PMID 25627786 DOI: 10.1021/Acs.Orglett.5B00038 |
0.55 |
|
| 2015 |
Zhu L, Liu Y, Ma R, Tong R. Total synthesis and structural revision of (+)-uprolide G acetate. Angewandte Chemie (International Ed. in English). 54: 627-32. PMID 25385395 DOI: 10.1002/Anie.201409618 |
0.542 |
|
| 2015 |
Zhu L, Tong R. Structural Revision of Uprolide G Acetate: Effective Interplay between NMR Data Analysis and Chemical Synthesis Synlett. 26: 1643-1648. DOI: 10.1055/S-0034-1380616 |
0.409 |
|
| 2015 |
Carreira EM, Zipfel HF, Zhu L, Liu Y, Ma R, Tong R. Synthesis and Structural Revision of (+)-Uprolide G Acetate Synfacts. 11: 120-120. DOI: 10.1055/S-0034-1379812 |
0.409 |
|
| 2015 |
Li Z, Ip FCF, Ip NY, Tong R. ChemInform Abstract: Highly trans-Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ-Deoxygenation and Heck-Matsuda Reaction: Asymmetric Total Synthesis of (-)-Musellarins A-C (I) and Their Analogues. Cheminform. 46: no-no. DOI: 10.1002/chin.201549201 |
0.428 |
|
| 2014 |
Yao H, Song L, Liu Y, Tong R. Cascade Michael addition/cycloketalization of cyclic 1,3-dicarbonyl compounds: important role of the tethered alcohol of α,β-unsaturated carbonyl compounds on reaction rate and regioselectivity. The Journal of Organic Chemistry. 79: 8774-85. PMID 25166284 DOI: 10.1021/Jo501604E |
0.371 |
|
| 2014 |
Li Z, Leung TF, Tong R. Total syntheses of (±)-musellarins A-C. Chemical Communications (Cambridge, England). 50: 10990-3. PMID 25096161 DOI: 10.1039/C4Cc05248J |
0.485 |
|
| 2014 |
Ren J, Tong R. Asymmetric total synthesis of (+)-didemniserinolipid B via Achmatowicz rearrangement/bicycloketalization. The Journal of Organic Chemistry. 79: 6987-95. PMID 25020037 DOI: 10.1021/Jo501142Q |
0.571 |
|
| 2014 |
Song L, Yao H, Tong R. Biomimetic asymmetric total syntheses of spirooliganones A and B. Organic Letters. 16: 3740-3. PMID 24971711 DOI: 10.1021/Ol501593M |
0.506 |
|
| 2014 |
Ren J, Liu Y, Song L, Tong R. Scalable asymmetric total syntheses of (+)-Psoracorylifol B and (+)-ent-Psoracorylifol C. Organic Letters. 16: 2986-9. PMID 24819702 DOI: 10.1021/Ol501120M |
0.52 |
|
| 2014 |
Song L, Lee KH, Lin Z, Tong R. Structural revision of cephalosporolide J and bassianolone. The Journal of Organic Chemistry. 79: 1493-7. PMID 24417265 DOI: 10.1021/Jo402602H |
0.328 |
|
| 2014 |
Yao H, Song L, Tong R. Total synthesis of aculeatin A via double intramolecular oxa-Michael addition of secondary/tertiary alcohols. The Journal of Organic Chemistry. 79: 1498-504. PMID 24393066 DOI: 10.1021/Jo4026868 |
0.48 |
|
| 2013 |
Song L, Liu Y, Tong R. Cephalosporolide B serving as a versatile synthetic precursor: asymmetric biomimetic total syntheses of cephalosporolides C, E, F, G, and (4-OMe-)G. Organic Letters. 15: 5850-3. PMID 24195739 DOI: 10.1021/Ol402913M |
0.403 |
|
| 2013 |
Ren J, Tong R. Convenient in situ generation of various dichlorinating agents from oxone and chloride: diastereoselective dichlorination of allylic and homoallylic alcohol derivatives. Organic & Biomolecular Chemistry. 11: 4312-5. PMID 23715511 DOI: 10.1039/C3Ob40670A |
0.349 |
|
| 2013 |
Song L, Yao H, Zhu L, Tong R. Asymmetric total syntheses of (-)-penicipyrone and (-)-tenuipyrone via biomimetic cascade intermolecular Michael addition/cycloketalization. Organic Letters. 15: 6-9. PMID 23249160 DOI: 10.1021/Ol303071T |
0.433 |
|
| 2013 |
Yao H, Ren J, Tong R. A short and flexible route to tetrahydropyran-4-ones via conjugated nitrile oxides cycloaddition and oxa-Michael cyclization: a concise diastereoselective total synthesis of (±)-diospongin A. Chemical Communications (Cambridge, England). 49: 193-5. PMID 23168684 DOI: 10.1039/C2Cc37772A |
0.494 |
|
| 2012 |
Zhu L, Song L, Tong R. Diastereoselective reductive ring expansion of spiroketal dihydropyranones to cis-fused bicyclic ethers. Organic Letters. 14: 5892-5. PMID 23163770 DOI: 10.1021/Ol302813E |
0.461 |
|
| 2012 |
Smith AB, Hoye AT, Martinez-Solorio D, Kim WS, Tong R. Unification of anion relay chemistry with the Takeda and Hiyama cross-coupling reactions: identification of an effective silicon-based transfer agent. Journal of the American Chemical Society. 134: 4533-6. PMID 22352347 DOI: 10.1021/Ja2120103 |
0.358 |
|
| 2012 |
McDonald FE, Tong R, Boone MA, Valentine JC. The adventure of abudinol and the misadventure of muzitone Strategies and Tactics in Organic Synthesis. 8: 225-260. DOI: 10.1016/B978-0-12-386540-3.00012-5 |
0.789 |
|
| 2012 |
Wein AN, Tong R, McDonald FE. An Economical Synthesis of 4‐Trimethylsilyl‐2‐Butyn‐1‐OL Organic Syntheses. 296-308. DOI: 10.1002/0471264229.Os088.27 |
0.633 |
|
| 2011 |
Smith AB, Tong R, Kim WS, Maio WA. Anion relay chemistry: Access to the type II ARC reaction manifold through a fundamentally different reaction pathway exploiting 1-oxa-2-silacyclopentanes and related congeners Angewandte Chemie - International Edition. 50: 8904-8907. PMID 21834108 DOI: 10.1002/Anie.201103886 |
0.335 |
|
| 2011 |
Wein AN, Tong R, McDonald FE. An economical synthesis of 4-trimethylsilyl-2-butyn-1-ol Organic Syntheses. 88: 296-308. DOI: 10.15227/orgsyn.088.0296 |
0.366 |
|
| 2010 |
Boone MA, Tong R, McDonald FE, Lense S, Cao R, Hardcastle KI. Biomimetic syntheses from squalene-like precursors: synthesis of ent-abudinol B and reassessment of the structure of muzitone. Journal of the American Chemical Society. 132: 5300-8. PMID 20334383 DOI: 10.1021/Ja1006806 |
0.77 |
|
| 2010 |
Smith AB, Kim WS, Tong R. Uniting anion relay chemistry with Pd-mediated cross coupling: design, synthesis and evaluation of bifunctional aryl and vinyl silane linchpins. Organic Letters. 12: 588-91. PMID 20028107 DOI: 10.1021/Ol902784Q |
0.369 |
|
| 2009 |
Tong R, Boone MA, McDonald FE. Stereo- and regioselective synthesis of squalene tetraepoxide. The Journal of Organic Chemistry. 74: 8407-9. PMID 19827774 DOI: 10.1021/Jo901920D |
0.77 |
|
| 2008 |
Tong R, McDonald FE. Mimicking biosynthesis: total synthesis of the triterpene natural product abudinol B from a squalene-like precursor. Angewandte Chemie (International Ed. in English). 47: 4377-9. PMID 18459096 DOI: 10.1002/Anie.200800749 |
0.703 |
|
| 2008 |
McDonald F, Tong R. Synthesis ofent-Abudinol B Synfacts. 2008: 1126-1126. DOI: 10.1055/S-0028-1083407 |
0.674 |
|
| 2007 |
Tong R, Valentine JC, McDonald FE, Cao R, Fang X, Hardcastle KI. Total syntheses of durgamone, nakorone, and abudinol B via biomimetic oxa- and carbacyclizations. Journal of the American Chemical Society. 129: 1050-1. PMID 17263384 DOI: 10.1021/Ja068826+ |
0.787 |
|
| 2007 |
McDonald FE, Tong R, Valentine JC, Bravo F. Biomimetic synthesis via polyepoxide cyclizations Pure and Applied Chemistry. 79: 281-291. DOI: 10.1351/Pac200779020281 |
0.785 |
|
| 2007 |
Tong R, McDonald FE, Fang X, Hardcastle KI. Biomimetic synthesis of fused bispyran: Lewis acid effects on oxacyclizations of polyepoxides Synthesis. 2337-2342. DOI: 10.1055/S-2007-983772 |
0.633 |
|
| 2007 |
Tong R, Valentine JC, McDonald FE, Cao R, Fang X, Hardcastle KI. Synthesis of Durgamone, Nakorone and Abudinol B Synfacts. 2007: 572-572. DOI: 10.1055/S-2007-968508 |
0.674 |
|
| 2007 |
McDonald FE, Tong R, Valentine JC, Bravo F. Biomimetic Synthesis via Polyepoxide Cyclizations Cheminform. 38. DOI: 10.1002/chin.200728271 |
0.774 |
|
| 2004 |
Guo CC, Tong RB, Li KL. Chloroalkyl piperazine and nitrogen mustard porphyrins: synthesis and anticancer activity. Bioorganic & Medicinal Chemistry. 12: 2469-75. PMID 15080942 DOI: 10.1016/J.Bmc.2004.01.045 |
0.401 |
|
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