| Year |
Citation |
Score |
| 2021 |
Zhu WR, Su Q, Deng XY, Liu JS, Zhong T, Meng SS, Yi JT, Weng J, Lu G. Organocatalytic enantioselective S1-type dehydrative nucleophilic substitution: access to bis(indolyl)methanes bearing quaternary carbon stereocenters. Chemical Science. 13: 170-177. PMID 35733509 DOI: 10.1039/d1sc05174a |
0.413 |
|
| 2020 |
Zhu WR, Su Q, Diao HJ, Wang EX, Wu F, Zhao YL, Weng J, Lu G. Enantioselective Dehydrative γ-Arylation of α-Indolyl Propargylic Alcohols with Phenols: Access to Chiral Tetrasubstituted Allenes and Naphthopyrans. Organic Letters. PMID 32808789 DOI: 10.1021/acs.orglett.0c02386 |
0.424 |
|
| 2020 |
Zhu WR, Liu K, Weng J, Huang WH, Huang WJ, Chen Q, Lin N, Lu G. Catalytic Asymmetric Synthesis of Vicinal Tetrasubstituted Diamines via Umpolung Cross-Mannich Reaction of Cyclic Ketimines. Organic Letters. PMID 32567863 DOI: 10.1021/acs.orglett.0c01578 |
0.478 |
|
| 2020 |
Zhong T, Pang MK, Chen ZD, Zhang B, Weng J, Lu G. Copper-free Sandmeyer-type Reaction for the Synthesis of Sulfonyl Fluorides. Organic Letters. PMID 32227908 DOI: 10.1021/acs.orglett.0c00823 |
0.317 |
|
| 2019 |
Xiong YS, Zhang B, Yu Y, Weng J, Lu G. Construction of sulfonyl phthalides via copper-catalyzed oxysulfonylation of 2-vinylbenzoic acids with sodium sulfinates. The Journal of Organic Chemistry. PMID 31545049 DOI: 10.1021/acs.joc.9b01646 |
0.337 |
|
| 2019 |
Zhu W, Zhang Z, Huang W, Lin N, Chen Q, Chen K, Wang B, Weng J, Lu G. Asymmetric Synthesis of Vicinally Bis(trifluoromethyl)-Substituted 3,3′-Pyrrolidinyl Spirooxindoles via Organocatalytic 1,3-Dipolar Cycloaddition Reactions Synthesis. 51: 1969-1979. DOI: 10.1055/S-0037-1612089 |
0.416 |
|
| 2019 |
Huang G, Huang W, Guo J, Xu D, Qu X, Zhai P, Zheng X, Weng J, Lu G. Enantioselective Synthesis of Triarylmethanes
via
Organocatalytic 1,6‐Addition of Arylboronic Acids to
para
‐Quinone Methides Advanced Synthesis & Catalysis. 361: 1241-1246. DOI: 10.1002/ADSC.201801446 |
0.306 |
|
| 2018 |
Guo J, Xie Y, Wu Q, Zeng W, Chan ASC, Weng J, Lu G. Copper-catalyzed aerobic decarboxylative coupling between cyclic α-amino acids and diverse C–H nucleophiles with low catalyst loading Rsc Advances. 8: 16202-16206. DOI: 10.1039/C8RA02340A |
0.317 |
|
| 2018 |
Zhu W, Chen Q, Lin N, Chen K, Zhang Z, Fang G, Weng J, Lu G. Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles Organic Chemistry Frontiers. 5: 1375-1380. DOI: 10.1039/C8QO00044A |
0.389 |
|
| 2018 |
Lin N, Long X, Chen Q, Zhu W, Wang B, Chen K, Jiang C, Weng J, Lu G. Highly efficient construction of chiral dispirocyclic oxindole/thiobutyrolactam/chromanone complexes through Michael/cyclization cascade reactions with a rosin-based squaramide catalyst Tetrahedron. 74: 3734-3741. DOI: 10.1016/J.TET.2018.05.052 |
0.457 |
|
| 2017 |
Guo J, Lin Z, Chen K, Xie Y, Chan ASC, Weng J, Lu G. Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids Organic Chemistry Frontiers. 4: 1400-1406. DOI: 10.1039/C7QO00129K |
0.435 |
|
| 2017 |
Huang W, Chen Q, Lin N, Long X, Pan W, Xiong Y, Weng J, Lu G. Asymmetric synthesis of trifluoromethyl-substituted 3,3′-pyrrolidinyl-dispirooxindoles through organocatalytic 1,3-dipolar cycloaddition reactions Organic Chemistry Frontiers. 4: 472-482. DOI: 10.1039/C6QO00723F |
0.404 |
|
| 2017 |
Liu C, Weng J, Lin Z, Huang W, Guo J, Huang L, Lu G. Asymmetric synthesis of vicinal amino alcohols via organocatalytic sequential α-amination/Grignard addition reactions of aldehydes Tetrahedron: Asymmetry. 28: 41-46. DOI: 10.1016/J.TETASY.2016.12.004 |
0.377 |
|
| 2016 |
Zhang J, Xiong Y, Chan ASC, Lu G. Cu(ii)-catalyzed cross-dehydrogenative coupling reaction of N′-acyl arylhydrazines and phosphites Rsc Advances. 6: 84587-84591. DOI: 10.1039/C6Ra13931K |
0.37 |
|
| 2016 |
Guo J, Weng J, Huang G, Huang L, Chan AS, Lu G. Indoxyl-based umpolung strategy for the synthesis of unsymmetrical 3,3′-biindoles Tetrahedron Letters. 57: 5493-5496. DOI: 10.1016/J.TETLET.2016.10.099 |
0.457 |
|
| 2016 |
Weng J, Huang LJ, Long L, Xu LY, Lu G. Enantioselective synthesis of syn-2-amino-1,3-diols via organocatalytic sequential oxa-Michael/α-amination reactions of α,β-unsaturated aldehydes Tetrahedron Letters. 57: 2554-2557. DOI: 10.1016/j.tetlet.2016.04.109 |
0.309 |
|
| 2016 |
Li JM, Weng J, Lu G, Chan ASC. Copper-catalyzed C5-regioselective C-H sulfonylation of 8-aminoquinoline amides with aryl sulfonyl chlorides Tetrahedron Letters. 57: 2121-2124. DOI: 10.1016/j.tetlet.2016.04.011 |
0.302 |
|
| 2015 |
Weng J, Wang S, Huang LJ, Luo ZY, Lu G. Stereoselective synthesis of epoxyisoprostanes: an organocatalytic and "pot-economy" approach. Chemical Communications (Cambridge, England). 51: 10170-3. PMID 26015997 DOI: 10.1039/c5cc01077b |
0.355 |
|
| 2015 |
Zhang JQ, Huang GB, Weng J, Lu G, Chan AS. Copper(ii)-catalyzed coupling reaction: an efficient and regioselective approach to N',N'-diaryl acylhydrazines. Organic & Biomolecular Chemistry. 13: 2055-63. PMID 25518836 DOI: 10.1039/c4ob02343a |
0.498 |
|
| 2014 |
Chen H, Huang L, Liu J, Weng J, Lu G. Synthesis of Terminal Vinylphosphonates Via Dbu-Promoted Tandem Phospha-Michael/Elimination Reactions Phosphorus, Sulfur, and Silicon and the Related Elements. 189: 1858-1866. DOI: 10.1080/10426507.2014.906422 |
0.326 |
|
| 2014 |
Feng YH, Luo RS, Nie L, Weng J, Lu G. Chiral diphenylperhydroindolinol silyl ether catalyzed domino oxa-Michael-aldol condensations for the asymmetric synthesis of benzopyrans Tetrahedron Asymmetry. 25: 523-528. DOI: 10.1016/j.tetasy.2014.02.016 |
0.416 |
|
| 2013 |
Deng Y, Zhang Z, Feng Y, Chan ASC, Lu G. ChemInform Abstract: Enantioselective Michael Reaction of Nitroalkanes onto Nitroalkenes Catalyzed by Cinchona Alkaloid Derivatives. Cheminform. 44: no-no. DOI: 10.1002/chin.201323022 |
0.425 |
|
| 2012 |
Liang DC, Luo RS, Yin LH, Chan AS, Lu G. A new synthetic route for axially chiral secondary amines with binaphthyl backbone and their applications in asymmetric Michael reaction of aldehydes to nitroalkenes. Organic & Biomolecular Chemistry. 10: 3071-9. PMID 22395306 DOI: 10.1039/c2ob07110j |
0.608 |
|
| 2012 |
Weng J, Ai HB, Luo RS, Lu G. Asymmetric Michael reaction of aldehydes with β-nitroalkenes catalyzed by pyrrolidine-camphor derived organocatalysts bearing hydrogen-bond donors. Chirality. 24: 271-5. PMID 22278901 DOI: 10.1002/chir.21991 |
0.34 |
|
| 2012 |
Deng Y, Zhang Z, Feng Y, Chan AS, Lu G. Enantioselective Michael reaction of nitroalkanes onto nitroalkenes catalyzed by cinchona alkaloid derivatives Tetrahedron: Asymmetry. 23: 1647-1652. DOI: 10.1016/j.tetasy.2012.11.008 |
0.57 |
|
| 2012 |
Weng J, Li Y, Wang R, Lu G. ChemInform Abstract: Organocatalytic Michael Reaction of Nitroenamine Derivatives with Aldehydes: Short and Efficient Asymmetric Synthesis of (-)-Oseltamivir. Cheminform. 43: no-no. DOI: 10.1002/chin.201245025 |
0.408 |
|
| 2012 |
Weng J, Li Y, Wang R, Lu G. Organocatalytic Michael Reaction of Nitroenamine Derivatives with Aldehydes: Short and Efficient Asymmetric Synthesis of (−)-Oseltamivir Chemcatchem. 4: 1007-1012. DOI: 10.1002/cctc.201200124 |
0.375 |
|
| 2011 |
Guo Z, Zhong S, Li Y, Lu G. Chiral 1,1′-binaphthylazepine derived amino alcohol catalyzed asymmetric Henry reaction Tetrahedron: Asymmetry. 22: 238-245. DOI: 10.1016/j.tetasy.2011.01.026 |
0.422 |
|
| 2011 |
Guo Z, Zhong S, Li Y, Lu G. ChemInform Abstract: Chiral 1,1′-Binaphthylazepine Derived Amino Alcohol Catalyzed Asymmetric Henry Reaction. Cheminform. 42: no-no. DOI: 10.1002/chin.201129023 |
0.426 |
|
| 2011 |
Lin N, Chen M, Luo R, Deng Y, Lu G. ChemInform Abstract: Indolinylmethanol Catalyzed Enantioselective Reformatsky Reaction with Ketones. Cheminform. 42: no-no. DOI: 10.1002/chin.201121050 |
0.409 |
|
| 2010 |
Weng J, Li YB, Wang RB, Li FQ, Liu C, Chan AS, Lu G. A practical and azide-free synthetic approach to oseltamivir from diethyl D-tartrate. The Journal of Organic Chemistry. 75: 3125-8. PMID 20394411 DOI: 10.1021/Jo100187M |
0.534 |
|
| 2010 |
Liu C, Guo ZL, Weng J, Lu G, Chan AS. Chiral 1,1'-binaphthylazepine-derived amino alcohol catalyzed asymmetric aryl transfer reactions with boroxine as aryl source. Chirality. 22: 159-64. PMID 19418552 DOI: 10.1002/chir.20721 |
0.615 |
|
| 2010 |
Nagano T, Jia Z, Li X, Yan M, Lu G, Chan ASC, Hayashi T. Redox Catalysis of Halide Ion for Formal Cross-dehydrogenative Coupling: Bromide Ion-catalyzed Direct Oxidative α-Acetoxylation of Ketones Chemistry Letters. 39: 929-931. DOI: 10.1246/Cl.2010.929 |
0.349 |
|
| 2010 |
Zhang Z, Lu G, Chen M, Lin N, Li Y, Hayashi T, Chan AS. Organocatalytic asymmetric Mannich-type reaction of N-sulfonylimines with isocyanoacetate leading to optically active 2-imidazoline-4-carboxylates Tetrahedron: Asymmetry. 21: 1715-1721. DOI: 10.1016/J.Tetasy.2010.04.029 |
0.555 |
|
| 2010 |
Luo R, Weng J, Ai H, Lu G, Chan ASC. ChemInform Abstract: Highly Efficient Asymmetric Michael Reaction of Aldehydes to Nitroalkenes with Diphenylperhydroindolinol Silyl Ethers as Organocatalysts. Cheminform. 41. DOI: 10.1002/chin.201006072 |
0.396 |
|
| 2010 |
Li F, Zhong S, Lu G, Chan ASC. ChemInform Abstract: Zinc-Salen-Catalyzed Asymmetric Alkynylation of Alkyl Acylsilanes. Cheminform. 41. DOI: 10.1002/chin.201002066 |
0.388 |
|
| 2010 |
Lu G, Li X, Zhou Z, Chan WL, Chan ASC. ChemInform Abstract: Enantioselective Alkynylation of Aromatic Aldehydes Catalyzed by New Chiral Amino Alcohol Based Ligands. Cheminform. 33: no-no. DOI: 10.1002/chin.200206083 |
0.405 |
|
| 2009 |
Li F, Zhong S, Lu G, Chan AS. Zinc-Salen-Catalyzed Asymmetric Alkynylation of Alkyl Acylsilanes Advanced Synthesis & Catalysis. 351: 2541-2541. DOI: 10.1002/adsc.200990030 |
0.567 |
|
| 2008 |
Ruan J, Lu G, Xu L, Li Y, Chan ASC. ChemInform Abstract: Catalytic Asymmetric Alkynylation and Arylation of Aldehydes by an H8-Binaphthyl-Based Amino Alcohol Ligand. Cheminform. 39. DOI: 10.1002/chin.200821070 |
0.355 |
|
| 2007 |
Li X, Lu G, Jia X, Wu Y, Chan AS. Highly enantioselective alkynylation of aldehydes using a new BINOL/Ti(OiPr)4/chiral sulfonamide catalyst system. Chirality. 19: 638-41. PMID 17554774 DOI: 10.1002/chir.20433 |
0.62 |
|
| 2007 |
Lu G, Li X, Li Y, Kwong FY, Chan ASC. Highly Enantioselective Catalytic Alkynylation of Ketones — A Convenient Approach to Optically Active Propargylic Alcohols. Cheminform. 38. DOI: 10.1002/Adsc.200606078 |
0.569 |
|
| 2006 |
Lu G, Kwong FY, Ruan JW, Li YM, Chan AS. Highly enantioselective addition of in situ prepared arylzinc to aldehydes catalyzed by a series of atropisomeric binaphthyl-derived amino alcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4115-20. PMID 16555357 DOI: 10.1002/Chem.200501048 |
0.643 |
|
| 2006 |
Lu G, Li X, Li YM, Kwong FY, Chan ASC. Highly enantioselective catalytic alkynylation of ketones - A convenient approach to optically active propargylic alcohols Advanced Synthesis and Catalysis. 348: 1926-1933. DOI: 10.1002/adsc.200606078 |
0.506 |
|
| 2005 |
LU G, LI Y, LI X, CHAN A. Synthesis and application of new chiral catalysts for asymmetric alkynylation reactions Coordination Chemistry Reviews. 249: 1736-1744. DOI: 10.1016/J.Ccr.2004.12.020 |
0.634 |
|
| 2004 |
Jia X, Li X, Lam WS, Kok SHL, Xu L, Lu G, Yeung CH, Chan ASC. The synthesis of new chiral phosphine-phosphinites, phosphine- phosphoramidite, and phosphine-phosphite ligands and their applications in asymmetric hydrogenation Tetrahedron Asymmetry. 15: 2273-2278. DOI: 10.1016/j.tetasy.2004.05.046 |
0.422 |
|
| 2004 |
Jia X, Li X, Lam WS, Kok SHL, Xu L, Lu G, Yeung C, Chan ASC. The Synthesis of New Chiral Phosphine—Phosphinites, Phosphine—Phosphoramidite, and Phosphine—Phosphite Ligands and Their Applications in Asymmetric Hydrogenation. Cheminform. 35. DOI: 10.1016/J.Tetasy.2004.05.046 |
0.51 |
|
| 2003 |
Lu G, Li X, Jia X, Chan WL, Chan AS. Enantioselective alkynylation of aromatic ketones catalyzed by chiral camphorsulfonamide ligands. Angewandte Chemie (International Ed. in English). 42: 5057-8. PMID 14595630 DOI: 10.1002/Anie.200352013 |
0.617 |
|
| 2003 |
Lu G, Li X, Chen G, Chan WL, Chan AS. Effective activation of chiral BINOL/Ti(OiPr)4 catalyst with phenolic additives for the enantioselective alkynylation of aldehydes Tetrahedron: Asymmetry. 14: 449-452. DOI: 10.1016/S0957-4166(03)00021-1 |
0.597 |
|
| 2003 |
Li X, Jia X, Lu G, Au-Yeung TT, Lam K, Lo TW, Chan AS. Highly enantioselective hydrogenation of enamides catalyzed by rhodium-monodentate phosphoramidite complex derived from H8-BINOL Tetrahedron: Asymmetry. 14: 2687-2691. DOI: 10.1016/J.Tetasy.2003.07.005 |
0.543 |
|
| 2003 |
Lu G, Li X, Chen G, Chan WL, Chan ASC. Effective Activation of Chiral BINOL/Ti(OiPr)4 Catalyst with Phenolic Additives for the Enantioselective Alkynylation of Aldehydes. Cheminform. 34. DOI: 10.1002/chin.200325039 |
0.417 |
|
| 2002 |
Li X, Lu G, Kwok WH, Chan AS. Highly enantioselective alkynylzinc addition to aromatic aldehydes catalyzed by self-assembled titanium catalysts. Journal of the American Chemical Society. 124: 12636-7. PMID 12392391 DOI: 10.1021/Ja025541Y |
0.61 |
|
| 2002 |
Lu G, Li X, Chan WL, Chan AS. Titanium-catalyzed enantioselective alkynylation of aldehydes. Chemical Communications (Cambridge, England). 172-3. PMID 12120356 DOI: 10.1039/B107817H |
0.606 |
|
| 2001 |
Lu G, Li X, Zhou Z, Chan WL, Chan AS. Enantioselective alkynylation of aromatic aldehydes catalyzed by new chiral amino alcohol-based ligands Tetrahedron: Asymmetry. 12: 2147-2152. DOI: 10.1016/S0957-4166(01)00384-6 |
0.59 |
|
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