| Year |
Citation |
Score |
| 2023 |
Xu W, Li X, Zou L, Li X, Zhang Z, Ali S, Wang Z, Li P, Zheng H. Access to Fully Substituted Dihydroindazoles Via Hexadehydro-Diels-Alder/[3 + 2] Cycloaddition. The Journal of Organic Chemistry. 88: 14736-14747. PMID 37819716 DOI: 10.1021/acs.joc.3c01901 |
0.307 |
|
| 2023 |
Zhang Z, Chen L, Wang Y, Dai W, Li P, Yang Z, Li X, Zheng H. Furan Synthesis via a Tandem 1,2-Acyloxy Migration/[3 + 2] Cycloaddition/Aromatization of Enol Ether-Tethered Propargylic Esters. The Journal of Organic Chemistry. PMID 37192482 DOI: 10.1021/acs.joc.3c00216 |
0.339 |
|
| 2023 |
Yu T, Yang J, Wang Z, Ding Z, Xu M, Wen J, Xu L, Li P. Selective [2σ + 2σ] Cycloaddition Enabled by Boronyl Radical Catalysis: Synthesis of Highly Substituted Bicyclo[3.1.1]heptanes. Journal of the American Chemical Society. PMID 36763965 DOI: 10.1021/jacs.2c13740 |
0.304 |
|
| 2023 |
Li L, Li P, Li T, Zhang M, Liu W, Li J, Wang L, Chen Y. Synthesis of the ABC ring system of kadlongilactones. Organic & Biomolecular Chemistry. PMID 36749621 DOI: 10.1039/d2ob01701f |
0.377 |
|
| 2020 |
Tong G, Ding Z, Liu Z, Ding YS, Xu L, Zhang H, Li P. Total synthesis of prostratin, a bioactive tigliane diterpenoid: access to multi-stereocenter cyclohexanes from a phenol. The Journal of Organic Chemistry. PMID 32166949 DOI: 10.1021/Acs.Joc.0C00022 |
0.397 |
|
| 2020 |
Zhan M, Ding Z, Du S, Chen H, Feng C, Xu M, Liu Z, Zhang M, Wu C, Lan Y, Li P. A unified approach for divergent synthesis of contiguous stereodiads employing a small boronyl group. Nature Communications. 11: 792. PMID 32034155 DOI: 10.1038/S41467-020-14592-7 |
0.363 |
|
| 2020 |
Ding Z, Liu Z, Tong G, Hu L, He Y, Bao Y, Lei Z, Zhang H, Li P. Facile synthesis of the daphnane and tigliane framework by semi-flow tube-based-bubbling photooxidation and diastereoselective conjugate addition Organic Chemistry Frontiers. 7: 1862-1868. DOI: 10.1039/D0Qo00424C |
0.373 |
|
| 2020 |
Zhan M, Song P, Jiao J, Li P. Novel Chiral Ligands‐Enabled Transition‐Metal‐Catalyzed Asymmetric C—H Borylation Chinese Journal of Chemistry. 38: 665-667. DOI: 10.1002/Cjoc.202000023 |
0.313 |
|
| 2019 |
Yang X, Zhang B, Zhang S, Li G, Xu L, Wang Z, Li P, Zhang Y, Liu Z, He G. The Marriage of Carborane with Chalcogen Atoms: Nonconjugation, σ-π Conjugation, and Intramolecular Charge Transfer. Organic Letters. PMID 31553197 DOI: 10.1021/Acs.Orglett.9B03047 |
0.316 |
|
| 2018 |
Mao S, Chen Z, Wang L, Khadka DB, Xin M, Li P, Zhang SQ. Synthesis of Aryl Trimethylstannane via BF3·OEt2-mediated Cross-Coupling of Hexaalkyl Distannane Reagent with Aryl Triazene at Room Temperature. The Journal of Organic Chemistry. PMID 30540911 DOI: 10.1021/Acs.Joc.8B02766 |
0.371 |
|
| 2018 |
Tong G, Liu Z, Li P. Total Synthesis of (±)-Prostratin Chem. 4: 2944-2954. DOI: 10.1016/J.Chempr.2018.10.002 |
0.356 |
|
| 2017 |
Liu L, Wang G, Jiao J, Li P. Sulfur-Directed Ligand-Free C-H Borylation by Iridium Catalysis. Organic Letters. PMID 29111752 DOI: 10.1021/Acs.Orglett.7B03008 |
0.3 |
|
| 2017 |
Hu D, Wang L, Li P. Decarboxylative Borylation of Aliphatic Esters under Visible-Light Photoredox Conditions. Organic Letters. PMID 28474531 DOI: 10.1021/Acs.Orglett.7B01181 |
0.353 |
|
| 2017 |
Ma GZ, Li PF, Liu L, Li WZ, Chen L. Diastereoselective Synthesis of Cephalotaxus Esters via Asymmetric Mukaiyama Aldol Reaction. Organic Letters. PMID 28409934 DOI: 10.1021/Acs.Orglett.7B00743 |
0.402 |
|
| 2017 |
Wang H, Wang G, Li P. Iridium-catalyzed intermolecular directed dehydrogenative ortho C–H silylation Organic Chemistry Frontiers. 4: 1943-1946. DOI: 10.1039/C7Qo00340D |
0.309 |
|
| 2017 |
Xu L, Wang G, Zhang S, Wang H, Wang L, Liu L, Jiao J, Li P. Recent advances in catalytic C−H borylation reactions Tetrahedron. 73: 7123-7157. DOI: 10.1016/J.Tet.2017.11.005 |
0.346 |
|
| 2016 |
Chen K, Zhang S, He P, Li P. Efficient metal-free photochemical borylation of aryl halides under batch and continuous-flow conditions. Chemical Science. 7: 3676-3680. PMID 30008997 DOI: 10.1039/C5Sc04521E |
0.331 |
|
| 2016 |
Wang G, Liu L, Wang H, Ding YS, Zhou J, Mao S, Li P. N,B-Bidentate Boryl Ligand-Supported Iridium Catalyst for Efficient Functional Group-Directed C-H Borylation. Journal of the American Chemical Society. PMID 27992177 DOI: 10.1021/Jacs.6B11867 |
0.321 |
|
| 2016 |
Zhang X, Zhang Q, Wu Y, Feng C, Xie C, Fan X, Li P. Polyaddition of Azide-Containing Norbornene-Based Monomer through Strain-Promoted 1,3-Dipolar Cycloaddition Reaction. Macromolecular Rapid Communications. PMID 27240093 DOI: 10.1002/Marc.201600233 |
0.32 |
|
| 2016 |
Chen K, He P, Zhang S, Li P. Synthesis of aryl trimethylstannanes from aryl halides: an efficient photochemical method. Chemical Communications (Cambridge, England). PMID 27020666 DOI: 10.1039/C6Cc01135G |
0.399 |
|
| 2016 |
Chen K, Cheung MS, Lin Z, Li P. Metal-free borylation of electron-rich aryl (pseudo)halides under continuous-flow photolytic conditions Organic Chemistry Frontiers. 3: 875-879. DOI: 10.1039/C6Qo00109B |
0.34 |
|
| 2016 |
Ding S, Xu L, Li P. Copper-Catalyzed Boron-Selective C(sp2)-C(sp3) Oxidative Cross-Coupling of Arylboronic Acids and Alkyltrifluoroborates Involving a Single-Electron Transmetalation Process Acs Catalysis. 6: 1329-1333. DOI: 10.1021/Acscatal.5B02524 |
0.315 |
|
| 2015 |
Xu L, Zhang S, Li P. Boron-selective reactions as powerful tools for modular synthesis of diverse complex molecules. Chemical Society Reviews. PMID 26393673 DOI: 10.1039/C5Cs00338E |
0.349 |
|
| 2015 |
Wang G, Xu L, Li P. Double N,B-Type Bidentate Boryl Ligands Enabling a Highly Active Iridium Catalyst for C-H Borylation. Journal of the American Chemical Society. 137: 8058-61. PMID 26079939 DOI: 10.1021/Jacs.5B05252 |
0.308 |
|
| 2015 |
Feng C, Wang H, Xu L, Li P. N-B dative bond-induced [3.3.0] bicyclic boronate-tethered exo-selective intramolecular Diels-Alder reaction. Organic & Biomolecular Chemistry. 13: 7136-9. PMID 26055829 DOI: 10.1039/C5Ob00917K |
0.345 |
|
| 2015 |
Xu L, Li P. Direct introduction of a naphthalene-1,8-diamino boryl [B(dan)] group by a Pd-catalysed selective boryl transfer reaction. Chemical Communications (Cambridge, England). 51: 5656-9. PMID 25715272 DOI: 10.1039/C5Cc00231A |
0.327 |
|
| 2015 |
Xu L, Zhang S, Li P. Synthesis of Silafluorenes and Silaindenes via Silyl Radicals from Arylhydrosilanes: Intramolecular Cyclization and Intermolecular Annulation with Alkynes Organic Chemistry Frontiers. 2: 459-463. DOI: 10.1039/C5Qo00012B |
0.422 |
|
| 2014 |
Tong G, Liu Z, Li P. Stereocontrolled construction of the tricyclic framework of tiglianes and daphnanes by an oxidative dearomatization approach. Organic Letters. 16: 2288-91. PMID 24742163 DOI: 10.1021/Ol5008263 |
0.349 |
|
| 2014 |
Xu L, Ding S, Li P. Site-differentiated polyboron arenes prepared by direct C-H borylation and their highly selective Suzuki-Miyaura cross-coupling reactions. Angewandte Chemie (International Ed. in English). 53: 1822-6. PMID 24505002 DOI: 10.1002/Anie.201309546 |
0.381 |
|
| 2014 |
Xu L, Li P. Differentiated Di- and Polyboron Compounds: Synthesis and Application in Successive Suzuki–Miyaura Coupling Synlett. 25: 1799-1802. DOI: 10.1055/S-0033-1339114 |
0.362 |
|
| 2013 |
Kretschmer M, Dieckmann M, Li P, Rudolph S, Herkommer D, Troendlin J, Menche D. Modular total synthesis of rhizopodin: a highly potent G-actin dimerizing macrolide. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 15993-6018. PMID 24123414 DOI: 10.1002/Chem.201302197 |
0.713 |
|
| 2013 |
Liu X, Xiong F, Huang X, Xu L, Li P, Wu X. Copper-catalyzed trifluoromethylation-initiated radical 1,2-aryl migration in α,α-diaryl allylic alcohols. Angewandte Chemie (International Ed. in English). 52: 6962-6. PMID 23712895 DOI: 10.1002/Anie.201302673 |
0.38 |
|
| 2012 |
Dieckmann M, Kretschmer M, Li P, Rudolph S, Herkommer D, Menche D. Total synthesis of rhizopodin. Angewandte Chemie (International Ed. in English). 51: 5667-70. PMID 22532514 DOI: 10.1002/anie.201201946 |
0.721 |
|
| 2011 |
Li P, Buchwald SL. Continuous-flow synthesis of 3,3-disubstituted oxindoles by a palladium-catalyzed α-arylation/alkylation sequence. Angewandte Chemie (International Ed. in English). 50: 6396-400. PMID 21656623 DOI: 10.1002/Anie.201102401 |
0.336 |
|
| 2010 |
Wang L, Li P, Menche D. Concise synthesis of tetrahydropyrans by a tandem oxa-Michael/Tsuji-Trost reaction. Angewandte Chemie (International Ed. in English). 49: 9270-3. PMID 20979071 DOI: 10.1002/Anie.201003304 |
0.637 |
|
| 2010 |
Morgen M, Bretzke S, Li P, Menche D. Stereodivergent synthesis of 1,3-syn- and -anti-tetrahydropyrimidinones. Organic Letters. 12: 4494-7. PMID 20831256 DOI: 10.1021/Ol101755M |
0.603 |
|
| 2010 |
Li P, Li J, Arikan F, Ahlbrecht W, Dieckmann M, Menche D. Stereoselective total synthesis of etnangien and etnangien methyl ester. The Journal of Organic Chemistry. 75: 2429-44. PMID 20334428 DOI: 10.1021/Jo100201F |
0.647 |
|
| 2010 |
Menche D, Li P, Irschik H. Design, synthesis and biological evaluation of simplified analogues of the RNA polymerase inhibitor etnangien. Bioorganic & Medicinal Chemistry Letters. 20: 939-41. PMID 20045639 DOI: 10.1016/J.Bmcl.2009.12.066 |
0.583 |
|
| 2010 |
Wang L, Li P, Menche D. Kurze Synthese von Tetrahydropyranen durch eine Oxa-Michael-Tsuji-Trost-Tandemreaktion Angewandte Chemie. 122: 9456-9460. DOI: 10.1002/Ange.201003304 |
0.624 |
|
| 2009 |
Li P, Li J, Arikan F, Ahlbrecht W, Dieckmann M, Menche D. Total synthesis of etnangien. Journal of the American Chemical Society. 131: 11678-9. PMID 19645468 DOI: 10.1021/Ja9056163 |
0.659 |
|
| 2009 |
Li P, Menche D. Cycloadditions in the total synthesis of sporolide B. Angewandte Chemie (International Ed. in English). 48: 5078-80. PMID 19514024 DOI: 10.1002/Anie.200901894 |
0.641 |
|
| 2009 |
Li J, Li P, Menche D. An efficient procedure for the direct nucleophilic substitution of the abiko-masamune auxiliary Synlett. 2417-2420. DOI: 10.1055/S-0029-1217819 |
0.582 |
|
| 2009 |
Li P, Menche D. Cycloadditionen in der Totalsynthese von Sporolid B Angewandte Chemie. 121: 5180-5182. DOI: 10.1002/Ange.200901894 |
0.499 |
|
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