Year |
Citation |
Score |
2022 |
Zhang YD, Li XY, Mo QK, Shi WB, Zhao JB, Zhu SF. Highly Regioselective Cobalt-Catalyzed Hydroboration of Internal Alkynes. Angewandte Chemie (International Ed. in English). 61: e202208473. PMID 35830204 DOI: 10.1002/anie.202208473 |
0.382 |
|
2021 |
Chen R, Qiu D, Lei X, Niu Y, Hua Y, Peng H, Zeng T, Zhang Y. Total Synthesis and Assignment of the Absolute Configuration of (+)-Omphalic Acid. Organic Letters. PMID 34397211 DOI: 10.1021/acs.orglett.1c02599 |
0.338 |
|
2021 |
Shen Y, Li L, Xiao X, Yang S, Hua Y, Wang Y, Zhang YW, Zhang Y. Site-Specific Photochemical Desaturation Enables Divergent Syntheses of Sesquiterpenes. Journal of the American Chemical Society. PMID 33600160 DOI: 10.1021/jacs.1c00525 |
0.303 |
|
2020 |
Jiang X, Zeng Z, Hua Y, Xu B, Shen Y, Xiong J, Qiu H, Wu Y, Hu T, Zhang Y. Merging C-H Vinylation with Switchable 6π-Electrocyclizations for Divergent Heterocycle Synthesis. Journal of the American Chemical Society. PMID 32786746 DOI: 10.1021/Jacs.0C07680 |
0.391 |
|
2020 |
Xu B, Jiang X, Xiong J, Lan J, Tian Y, Zhong L, Wang X, Xu N, Cao H, Zhang W, Zhang H, Hong X, Zhan YY, Zhang Y, Hu T. Structure-Activity Relationship Study Enables the Discovery of a Novel Berberine Analogue as RXRα Activator to Inhibit Colon Cancer. Journal of Medicinal Chemistry. PMID 32391701 DOI: 10.1021/Acs.Jmedchem.0C00088 |
0.311 |
|
2020 |
Chen R, Shen Y, Yang S, Zhang Y. Conformational Design Principles in Total Synthesis. Angewandte Chemie (International Ed. in English). PMID 32285522 DOI: 10.1002/Anie.202003735 |
0.372 |
|
2020 |
Chen R, Yang S, Zhang Y. Recent progress in the total synthesis of marine brominated sesquiterpene aplydactone. Organic & Biomolecular Chemistry. PMID 31961356 DOI: 10.1039/C9Ob02642H |
0.408 |
|
2020 |
Zhang F, Niu Y, Hong D, Ye Y, Hua Y, Ding S, Zhang Y. Synthetic studies towards atkamine Chinese Chemical Letters. DOI: 10.1016/J.Cclet.2020.06.008 |
0.44 |
|
2019 |
Xie CL, Chen R, Yang S, Xia JM, Zhang GY, Chen CH, Zhang Y, Yang XW. Nesteretal A, A Novel Class of Cage-Like Polyketide from Marine-Derived Actinomycete . Organic Letters. PMID 31423796 DOI: 10.1021/Acs.Orglett.9B02634 |
0.31 |
|
2019 |
Zeng Z, Zhao Y, Zhang Y. Divergent total syntheses of five illudalane sesquiterpenes and assignment of the absolute configuration. Chemical Communications (Cambridge, England). PMID 30901009 DOI: 10.1039/C9Cc00933G |
0.451 |
|
2019 |
Lin M, Cui H, Hua Y, Zhang Y. Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F Organic Chemistry Frontiers. 6: 2771-2774. DOI: 10.1039/C9Qo00477G |
0.454 |
|
2018 |
Chen R, Li L, Lin N, Zhou R, Hua Y, Deng H, Zhang Y. Asymmetric Total Synthesis of (+)-Majusculoic Acid via a Dimerization-Dedimerization Strategy and Absolute Configuration Assignment. Organic Letters. PMID 29446640 DOI: 10.1021/Acs.Orglett.8B00349 |
0.395 |
|
2018 |
Li J, Ye Y, Zhang Y. Cycloaddition/annulation strategies for the construction of multisubstituted pyrrolidines and their applications in natural product synthesis Organic Chemistry Frontiers. 5: 864-892. DOI: 10.1039/C7Qo01077J |
0.442 |
|
2018 |
Zeng Z, Chen C, Zhang Y. Enantioselective total synthesis of periconiasin A Organic Chemistry Frontiers. 5: 838-840. DOI: 10.1039/C7Qo00952F |
0.504 |
|
2017 |
Lin M, Cai PJ, Zeng Z, Lin N, Shen Y, Tang B, Li F, Chen C, Yu ZX, Zhang Y. Conformational Bias by a Removable Silyl Group: Construction of Bicyclo[n.3.1]alkenes via Ring Closing Metathesis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29119609 DOI: 10.1002/Chem.201705275 |
0.442 |
|
2017 |
Han YC, Zhang YD, Jia Q, Cui J, Zhang C. Hypervalent-Iodine-Mediated Ring-Contraction Monofluorination Affording Monofluorinated Five-Membered Ring-Fused Oxazolines. Organic Letters. PMID 28926269 DOI: 10.1021/acs.orglett.7b02479 |
0.415 |
|
2017 |
Liu C, Chen R, Shen Y, Liang Z, Hua Y, Zhang Y. Total Synthesis of Aplydactone via a Conformationally Controlled C-H Functionalization. Angewandte Chemie (International Ed. in English). PMID 28467008 DOI: 10.1002/Anie.201703803 |
0.38 |
|
2017 |
Lin M, Cai P, Zeng Z, Lin N, Shen Y, Tang B, Li F, Chen C, Yu Z, Zhang Y. Cover Feature: Conformational Bias by a Removable Silyl Group: Construction of Bicyclo[n
.3.1]alkenes by Ring Closing Metathesis (Chem. Eur. J. 10/2018) Chemistry - a European Journal. 24: 2293-2293. DOI: 10.1002/Chem.201705829 |
0.355 |
|
2017 |
Liu C, Chen R, Shen Y, Liang Z, Hua Y, Zhang Y. Inside Cover: Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization (Angew. Chem. Int. Ed. 28/2017) Angewandte Chemie. 56: 8018-8018. DOI: 10.1002/Anie.201705178 |
0.345 |
|
2017 |
Liu C, Chen R, Shen Y, Liang Z, Hua Y, Zhang Y. Innentitelbild: Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization (Angew. Chem. 28/2017) Angewandte Chemie. 129: 8130-8130. DOI: 10.1002/Ange.201705178 |
0.359 |
|
2016 |
Liu C, Zeng Z, Chen R, Jiang X, Wang Y, Zhang Y. Total Synthesis of (+)-Fusarisetin A Driven by a One-Pot Four-Reaction Process. Organic Letters. PMID 26812626 DOI: 10.1021/Acs.Orglett.6B00036 |
0.486 |
|
2016 |
Li J, Lin N, Yu L, Zhang Y. Synthesis of β -prolinols via [3+2] cycloaddition and one-pot programmed reduction: Valuable building blocks for polyheterocycles Tetrahedron Letters. 57: 5777-5780. DOI: 10.1016/J.Tetlet.2016.11.035 |
0.322 |
|
2015 |
Shen Y, Li L, Pan Z, Wang Y, Li J, Wang K, Wang X, Zhang Y, Hu T, Zhang Y. Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans. Organic Letters. PMID 26509873 DOI: 10.1021/Acs.Orglett.5B02845 |
0.473 |
|
2015 |
Li J, Zhao H, Jiang X, Wang X, Hu H, Yu L, Zhang Y. The cyano group as a traceless activation group for the intermolecular [3+2] cycloaddition of azomethine ylides: a five-step synthesis of (±)-isoretronecanol. Angewandte Chemie (International Ed. in English). 54: 6306-10. PMID 25820905 DOI: 10.1002/Anie.201500961 |
0.455 |
|
2015 |
Li J, Zhao H, Zhang Y. Recent Progress in the Synthesis of 5-Unsubstituted Pyrrolidines via [3+2] Cycloadditions Synlett. 26: 2745-2750. DOI: 10.1055/S-0035-1560178 |
0.44 |
|
2012 |
Sun TW, Ren WW, Xiao Q, Tang YF, Zhang YD, Li Y, Meng FK, Liu YF, Zhao MZ, Xu LM, Chen JH, Yang Z. Diastereoselective total synthesis of (±)-schindilactone A, Part 1: Construction of the ABC and FGH ring systems and initial attempts to construct the CDEF ring system. Chemistry, An Asian Journal. 7: 2321-33. PMID 22761005 DOI: 10.1002/Asia.201200363 |
0.684 |
|
2011 |
Chou TC, Dong H, Zhang X, Lei X, Hartung J, Zhang Y, Lee JH, Wilson RM, Danishefsky SJ. Multifaceted cytoprotection by synthetic polyacetylenes inspired by the ginseng-derived natural product, panaxytriol. Proceedings of the National Academy of Sciences of the United States of America. 108: 14336-41. PMID 21844359 DOI: 10.1073/Pnas.1111332108 |
0.58 |
|
2011 |
Zhang Y, Lee JH, Danishefsky SJ. Antarafacial mediation of oxygen delivery by a phenylsulfinyl group in the epoxidation of proximal double bonds: intramolecular trapping of an early Pummerer intermediate with stereoelectronic control. Journal of the American Chemical Society. 133: 752-5. PMID 21182300 DOI: 10.1021/Ja1107707 |
0.599 |
|
2010 |
Lee JH, Zhang Y, Danishefsky SJ. A straightforward route to functionalized trans-Diels-Alder motifs. Journal of the American Chemical Society. 132: 14330-3. PMID 20863105 DOI: 10.1021/Ja1073855 |
0.614 |
|
2010 |
Zhang Y, Danishefsky SJ. Total synthesis of (+/-)-aplykurodinone-1: traceless stereochemical guidance. Journal of the American Chemical Society. 132: 9567-9. PMID 20513158 DOI: 10.1021/Ja1035495 |
0.524 |
|
2008 |
Zhang YD, Ren WW, Lan Y, Xiao Q, Wang K, Xu J, Chen JH, Yang Z. Stereoselective construction of an unprecedented 7-8 fused ring system in micrandilactone a by [3,3]-sigmatropic rearrangement. Organic Letters. 10: 665-8. PMID 18215052 DOI: 10.1021/Ol703126Q |
0.499 |
|
2006 |
Zhang Y, Tang Y, Luo T, Shen J, Chen aJ, Yang Z. Application of RCM reaction in the construction of ABC ring of micrandilactone A. Organic Letters. 8: 107-110. PMID 16381579 DOI: 10.1021/Ol052630H |
0.563 |
|
2005 |
Tang Y, Zhang Y, Dai M, Luo T, Deng L, Chen J, Yang Z. A highly efficient synthesis of the FGH ring of micrandilactone A. Application of thioureas as ligands in the Co-catalyzed Pauson-Khand reaction and Pd-catalyzed carbonylative annulation. Organic Letters. 7: 885-8. PMID 15727466 DOI: 10.1021/Ol047394+ |
0.624 |
|
2005 |
Tang Y, Deng L, Zhang Y, Dong G, Chen J, Yang Z. Tetramethyl thiourea/Co2(CO)8-catalyzed Pauson-Khand reaction under balloon pressure of CO. Organic Letters. 7: 593-5. PMID 15704902 DOI: 10.1021/Ol047651A |
0.466 |
|
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