Year |
Citation |
Score |
2024 |
Liu M, Wu C, Xie X, Li H, She X. Total Synthesis of the Euphorbia Diterpenoid Pepluacetal. Angewandte Chemie (International Ed. in English). e202400943. PMID 38509839 DOI: 10.1002/anie.202400943 |
0.718 |
|
2023 |
Wu C, Zhang J, Liu M, Xie X, Li H, She X. Rearrangement of the Tetra- and Tricyclic Skeletons of Pepluanol B to Access the Core Structures of Tigliane- and Myrsinane-Type Diterpenes. Organic Letters. 25: 7995-7999. PMID 37906267 DOI: 10.1021/acs.orglett.3c03109 |
0.689 |
|
2023 |
Duan X, Xu H, Shen Y, Liu A, He F, Hou H, Li H, Xie X, She X. Synthesis of the 5-6-7 Tricyclic Core of Daphnicyclidin-Type Alkaloids via a Tiffeneau-Demjanov Ring Enlargement Strategy. The Journal of Organic Chemistry. 88: 14842-14846. PMID 37800749 DOI: 10.1021/acs.joc.3c01895 |
0.752 |
|
2023 |
Shi H, Hou H, Duan J, Huang J, Duan X, Xie X, Li H, She X. Total Syntheses of Phleghenrines A and C: A [4 + 2] Cycloaddition and Ring-Expansion Approach. Organic Letters. PMID 37010229 DOI: 10.1021/acs.orglett.3c00755 |
0.782 |
|
2023 |
Yang H, Zhang Y, Chen W, Shi H, Huo L, Li J, Li H, Xie X, She X. Scalable Total Syntheses of (±)-Catellatolactams A and B. Organic Letters. PMID 36748956 DOI: 10.1021/acs.orglett.3c00132 |
0.749 |
|
2022 |
Zhao Y, Li J, Ma R, He F, Shi H, Duan X, Li H, Xie X, She X. Ten-Step Total Synthesis of (-)-Andranginine. Organic Letters. 24: 6880-6883. PMID 36098548 DOI: 10.1021/acs.orglett.2c02927 |
0.801 |
|
2022 |
Chen J, Yang Y, Wu C, Huo L, Xie X, Li H, She X. Diastereoselective Synthesis of 1-Hydroxyl Allogibberic Methyl Ester to Diverse Bioactive Molecules. Organic Letters. PMID 36017965 DOI: 10.1021/acs.orglett.2c02422 |
0.757 |
|
2022 |
Wang P, Gong Y, Wang X, Ren Y, Wang L, Zhai L, Li H, She X. Solvent-free, B(C6F5)3-Catalyzed S-H Insertion of Thiophenols and Thiols with α-Diazoesters. Chemistry, An Asian Journal. PMID 35678551 DOI: 10.1002/asia.202200465 |
0.592 |
|
2022 |
He F, Feng S, Zhao Y, Shi H, Duan X, Li H, Xie X, She X. Collective Total Syntheses of Five Lycopodium Alkaloids. Angewandte Chemie (International Ed. in English). PMID 35596233 DOI: 10.1002/anie.202205439 |
0.765 |
|
2022 |
Wang L, Zhai L, Chen J, Gong Y, Wang P, Li H, She X. Catalyst-Free 1,2-Dibromination of Alkenes Using 1,3-Dibromo-5,5-dimethylhydantoin (DBDMH) as a Bromine Source. The Journal of Organic Chemistry. PMID 35133816 DOI: 10.1021/acs.joc.1c02906 |
0.555 |
|
2021 |
Xu LW, Li HL, Huang WS, Ling FY, Li L, Yan JH, Xu H. Highly Diastereoselective Hydrosilane-assisted Rhodium-Catalyzed Spiro-type Cycloisomerization of Succinimide and Pyrazolone -based Functional 1,6-Dienes. Chemistry, An Asian Journal. PMID 33945231 DOI: 10.1002/asia.202100372 |
0.425 |
|
2020 |
She X, Li H, Zhang J. Recent Advances in Total Synthesis of Diquinane-Containing Natural Products. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32955141 DOI: 10.1002/Chem.202003741 |
0.571 |
|
2020 |
Chen P, Yang H, Zhang H, Chen W, Zhang Z, Zhang J, Li H, Wang X, Xie X, She X. Total Synthesis of (-)-Gardmultimine A. Organic Letters. PMID 32096647 DOI: 10.1021/Acs.Orglett.0C00399 |
0.768 |
|
2020 |
Zhang H, Chen P, Yang H, Ma S, Wang Z, Xie X, Wang X, Li H, She X. A Strategy to Construct cis-Hydrocarbazole via Nickel/Lewis Acid Dual-Catalyzed Arylcyanation. The Journal of Organic Chemistry. PMID 31994398 DOI: 10.1021/Acs.Joc.9B03243 |
0.715 |
|
2020 |
Zhang J, Liu M, Wu C, Zhao G, Chen P, Zhou L, Xie X, Fang R, Li H, She X. Total Synthesis of (-)-Pepluanol B: Conformational Control of the Eight-Membered Ring System. Angewandte Chemie (International Ed. in English). PMID 31898399 DOI: 10.1002/Anie.201915876 |
0.778 |
|
2020 |
Ma S, Long D, Chen P, Shi H, Li H, Fang R, Wang X, Xie X, She X. Synthesis of 2,3-disubstituted indoles via a tandem reaction Organic Chemistry Frontiers. 7: 2689-2695. DOI: 10.1039/D0Qo00765J |
0.769 |
|
2019 |
Liu Z, Ju X, Ma S, Du C, Zhang W, Li H, Wang X, Xie X, She X. Asymmetric Total Synthesis of (+)-Winchinine B. The Journal of Organic Chemistry. PMID 31646864 DOI: 10.1021/Acs.Joc.9B02462 |
0.788 |
|
2019 |
Du C, Fang J, Chen J, Liu Z, Li H, Wang X, Xie X, She X. Construction of the Tetracyclic Core of Calyciphylline B-Type Alkaloids. Organic Letters. PMID 31613108 DOI: 10.1021/Acs.Orglett.9B03322 |
0.787 |
|
2019 |
Feng S, Li J, He F, Li T, Li H, Wang X, Xie X, She X. A copper-catalyzed radical coupling/fragmentation reaction: efficient access to β-oxophosphine oxides Organic Chemistry Frontiers. 6: 946-951. DOI: 10.1039/C9Qo00006B |
0.714 |
|
2019 |
He M, Yi J, Zhao G, Chen P, Long D, Hu X, Li H, Xie X, Wang X, She X. A concise approach to the tricyclic framework of longipinane- and ent-longipinane-type sesquiterpenoids Organic Chemistry Frontiers. 6: 383-387. DOI: 10.1039/C8Qo01235K |
0.705 |
|
2018 |
Zhang W, Lin S, Du C, Feng S, Liu Z, Zhang J, Xie X, Wang X, Li H, She X. Total Synthesis of Aspidofractinine Alkaloid Paucidirinine. The Journal of Organic Chemistry. PMID 30562463 DOI: 10.1021/Acs.Joc.8B03023 |
0.791 |
|
2018 |
Chen P, Huo L, Li H, Liu L, Yuan Z, Zhang H, Feng S, Xie X, Wang X, She X. Bioinspired total synthesis of (−)-gymnothelignan L Organic Chemistry Frontiers. 5: 1124-1128. DOI: 10.1039/C8Qo00026C |
0.76 |
|
2017 |
Li H, Lu Y. Enantioselective Construction of All‐Carbon Quaternary Stereogenic Centers by Using Phosphine Catalysis Asian Journal of Organic Chemistry. 6: 1130-1145. DOI: 10.1002/Ajoc.201700220 |
0.404 |
|
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 |
0.488 |
|
2015 |
Zhao G, He M, Li H, Duan S, Yuan Z, Xie X, She X. Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework. Chemical Communications (Cambridge, England). PMID 26463746 DOI: 10.1039/C5Cc06923H |
0.77 |
|
2015 |
Zhong Z, Ma D, Zhao G, Li H, Xu D, Xie X, She X. Asymmetric Total Synthesis of (-)-Kravanhin B. Chemistry, An Asian Journal. PMID 26398294 DOI: 10.1002/Asia.201500860 |
0.792 |
|
2014 |
Zhao C, Xie X, Duan S, Li H, Fang R, She X. Gold-catalyzed 1,2-acyloxy migration/intramolecular [3+2] 1,3-dipolar cycloaddtion cascade reaction: an efficient strategy for syntheses of medium-sized-ring ethers and amines. Angewandte Chemie (International Ed. in English). 53: 10789-93. PMID 25111560 DOI: 10.1002/Anie.201406486 |
0.78 |
|
2014 |
Li H, Zhang Y, Xie X, Ma H, Zhao C, Zhao G, She X. Bioinspired total synthesis of gymnothelignan N. Organic Letters. 16: 4440-3. PMID 25103476 DOI: 10.1021/Ol501960J |
0.782 |
|
2014 |
Xu S, Gu J, Li H, Ma D, Xie X, She X. Enantioselective total synthesis of (-)-walsucochin B. Organic Letters. 16: 1996-9. PMID 24670038 DOI: 10.1021/Ol500553X |
0.759 |
|
2014 |
Li H, Qiu Y, Zhao C, Yuan Z, Xie X, She X. Diels-Alder/oxidative aromatization approach towards the all-carbon DEF tricyclic skeleton of daphenylline. Chemistry, An Asian Journal. 9: 1274-7. PMID 24591463 DOI: 10.1002/Asia.201400002 |
0.766 |
|
2014 |
Zhao C, Yuan Z, Zhang Y, Ma B, Li H, Tang S, Xie X, She X. Scalable, efficient total synthesis of (+)-mupirocin H Organic Chemistry Frontiers. 1: 105-108. DOI: 10.1039/C3Qo00038A |
0.731 |
|
2013 |
Fang B, Xie X, Zhao C, Jing P, Li H, Wang Z, Gu J, She X. Asymmetric total synthesis of fusarentin 6-methyl ether and its biomimetic transformation into fusarentin 6,7-dimethyl ether, 7-O-demethylmonocerin, and (+)-monocerin. The Journal of Organic Chemistry. 78: 6338-43. PMID 23713975 DOI: 10.1021/Jo400760Q |
0.72 |
|
2013 |
Ma B, Zhong Z, Hu H, Li H, Zhao C, Xie X, She X. Concise enantioselective synthesis of cephalosporolide B, (4R)-4-OMe-cephalosporolide C, and (4S)-4-OMe-cephalosporolide C. Chemistry, An Asian Journal. 8: 1391-4. PMID 23650094 DOI: 10.1002/Asia.201300332 |
0.783 |
|
2013 |
Huo X, Zhao C, Zhao G, Tang S, Li H, Xie X, She X. PtCl2-catalyzed tandem enyne cyclization/1,2 ester migration reaction controlled by substituent effects of all-carbon 1,6-enynyl esters. Chemistry, An Asian Journal. 8: 892-5. PMID 23427008 DOI: 10.1002/Asia.201300018 |
0.76 |
|
2013 |
Ma D, Zhao C, Li H, Qi J, Zhang L, Xu S, Xie X, She X. Concise formal syntheses of the Amaryllidaceae alkaloids (±)-tazettine and (±)-6a-epipretazettine: construction of the core skeleton via tandem intramolecular oxidative Friedel-Crafts/aza-Michael reaction. Chemistry, An Asian Journal. 8: 364-8. PMID 23197428 DOI: 10.1002/Asia.201200964 |
0.683 |
|
2013 |
Fang B, Xie X, Li H, Jing P, Gu J, She X. Asymmetric total synthesis of (+)-monocerin Tetrahedron Letters. 54: 6349-6351. DOI: 10.1016/J.Tetlet.2013.09.055 |
0.77 |
|
2013 |
Fang B, Xie X, Jing P, Zhao C, Li H, Ma H, She X. Biomimetically inspired total synthesis of (12S)-12-hydroxymonocerin and (12R)-12-hydroxymonocerin Tetrahedron. 69: 11025-11030. DOI: 10.1016/J.Tet.2013.09.075 |
0.75 |
|
2012 |
Li H, Zheng J, Xu S, Ma D, Zhao C, Fang B, Xie X, She X. Rapid construction of the [6-6-6-5] tetracyclic skeleton of the Daphniphyllum alkaloid daphenylline. Chemistry, An Asian Journal. 7: 2519-22. PMID 22945890 DOI: 10.1002/Asia.201200625 |
0.738 |
|
2012 |
Fang B, Zheng H, Zhao C, Jing P, Li H, Xie X, She X. Synthesis of the tetracyclic core (ABCE rings) of daphenylline. The Journal of Organic Chemistry. 77: 8367-73. PMID 22934890 DOI: 10.1021/Jo301533F |
0.781 |
|
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