| Year |
Citation |
Score |
| 2022 |
Xiao YQ, Li MM, Zhou ZX, Li YJ, Cao MY, Liu XP, Lu HH, Li R, Lu LQ, Beauchemin AM, Xiao WJ. Taming Chiral Quaternary Stereocenters via Remote H-Bonding Stereoinduction in Palladium-Catalyzed (3+2) Cycloadditions. Angewandte Chemie (International Ed. in English). PMID 36377924 DOI: 10.1002/anie.202212444 |
0.522 |
|
| 2022 |
Lu HH, Gan KJ, Ni FQ, Zhang Z, Zhu Y. Concise Total Synthesis of Salimabromide. Journal of the American Chemical Society. PMID 36194507 DOI: 10.1021/jacs.2c08337 |
0.462 |
|
| 2022 |
Cao MY, Ma BJ, Gu QX, Fu B, Lu HH. Concise Enantioselective Total Synthesis of Daphenylline Enabled by an Intramolecular Oxidative Dearomatization. Journal of the American Chemical Society. 144: 5750-5755. PMID 35289615 DOI: 10.1021/jacs.2c01674 |
0.471 |
|
| 2020 |
Cao MY, Ma BJ, Lao ZQ, Wang H, Wang J, Liu J, Xing K, Huang YH, Gan KJ, Gao W, Wang H, Hong X, Lu HH. Optically Active Flavaglines-Inspired Molecules by a Palladium-Catalyzed Decarboxylative Dearomative Asymmetric Allylic Al-kylation. Journal of the American Chemical Society. PMID 32584568 DOI: 10.1021/jacs.0c05113 |
0.374 |
|
| 2018 |
Witkin JM, Shenvi RA, Li X, Gleason SD, Weiss J, Morrow D, Catow JT, Wakulchik M, Ohtawa M, Lu HH, Martinez MD, Schkeryantz JM, Carpenter TS, Lightstone FC, Cerne R. Pharmacological characterization of the neurotrophic sesquiterpene jiadifenolide reveals a non-convulsant signature and potential for progression in neurodegenerative disease studies. Biochemical Pharmacology. PMID 29940173 DOI: 10.1016/J.Bcp.2018.06.022 |
0.537 |
|
| 2016 |
Lu HH, Pronin SV, Antonova-Koch Y, Meister S, Winzeler EA, Shenvi RA. Synthesis of (+)-7,20-Diisocyanoadociane and Liver-Stage Antiplasmodial Activity of the Isocyanoterpene Class. Journal of the American Chemical Society. PMID 27244042 DOI: 10.1021/Jacs.6B03899 |
0.615 |
|
| 2015 |
Lu HH, Hinkelmann B, Tautz T, Li J, Sasse F, Franke R, Kalesse M. Paleo-soraphens: chemical total syntheses and biological studies. Organic & Biomolecular Chemistry. PMID 26119264 DOI: 10.1039/C5Ob01249J |
0.546 |
|
| 2015 |
Lu HH, Martinez MD, Shenvi RA. An eight-step gram-scale synthesis of (-)-jiadifenolide. Nature Chemistry. 7: 604-7. PMID 26100810 DOI: 10.1038/Nchem.2283 |
0.623 |
|
| 2014 |
Kalesse M, Cordes M, Symkenberg G, Lu HH. The vinylogous Mukaiyama aldol reaction (VMAR) in natural product synthesis. Natural Product Reports. 31: 563-94. PMID 24595879 DOI: 10.1039/C3Np70102F |
0.606 |
|
| 2013 |
Lu HH, Raja A, Franke R, Landsberg D, Sasse F, Kalesse M. Synthesis and biological evaluation of paleo-soraphens. Angewandte Chemie (International Ed. in English). 52: 13549-52. PMID 24346938 DOI: 10.1002/Anie.201305331 |
0.57 |
|
| 2010 |
Zhang FG, Yang QQ, Xuan J, Lu HH, Duan SW, Chen JR, Xiao WJ. Enantioselective conjugate addition of oximes to trisubstituted β-nitroacrylates: an organocatalytic approach to β(2,2)-amino acid derivatives. Organic Letters. 12: 5636-9. PMID 21080696 DOI: 10.1021/ol102580n |
0.469 |
|
| 2009 |
Lu HH, Zhang FG, Meng XG, Duan SW, Xiao WJ. Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters. Organic Letters. 11: 3946-9. PMID 19653671 DOI: 10.1021/ol901572x |
0.471 |
|
| 2009 |
Lu HH, Wang XF, Yao CJ, Zhang JM, Wu H, Xiao WJ. Highly enantioselective organocatalytic Michael addition of nitroalkanes to 4-oxo-enoates. Chemical Communications (Cambridge, England). 4251-3. PMID 19585037 DOI: 10.1039/b905033g |
0.52 |
|
| 2009 |
Lu HH, Liu H, Wu W, Wang XF, Lu LQ, Xiao WJ. Catalytic asymmetric intramolecular hydroarylations of omega-aryloxy- and arylamino-tethered alpha,beta-unsaturated aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 2742-6. PMID 19204966 DOI: 10.1002/chem.200802722 |
0.484 |
|
| 2005 |
Chen JR, Lu HH, Li XY, Cheng L, Wan J, Xiao WJ. Readily tunable and bifunctional L-prolinamide derivatives: design and application in the direct enantioselective Aldol reactions. Organic Letters. 7: 4543-5. PMID 16178579 DOI: 10.1021/ol0520323 |
0.525 |
|
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