| Year |
Citation |
Score |
| 2021 |
Huang L, Xie JH, Cai Y, Zheng C, Hou XL, Dai LX, You SL. Enantioselective synthesis of polycyclic pyrrole derivatives by iridium-catalyzed asymmetric allylic dearomatization and ring-expansive migration reactions. Chemical Communications (Cambridge, England). PMID 33949525 DOI: 10.1039/d1cc01929e |
0.851 |
|
| 2019 |
Li AH, Dai LX, Aggarwal VK. Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement. Chemical Reviews. 97: 2341-2372. PMID 11848902 DOI: 10.1021/Cr960411R |
0.566 |
|
| 2018 |
Gao RD, Ding L, Zheng C, Dai LX, You SL. Palladium(0)-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Polycyclic Indoles. Organic Letters. PMID 29368933 DOI: 10.1021/Acs.Orglett.7B03887 |
0.798 |
|
| 2017 |
You S, Yi JC, Liu C, Dai LX. Synthesis of C3 Methyl Substituted Pyrroloindolines and Furoindolines via Cascade Dearomatization of Indole Derivatives with Methyl Iodide. Chemistry, An Asian Journal. PMID 28967186 DOI: 10.1002/Asia.201701151 |
0.685 |
|
| 2017 |
You S, Huang L, Cai Y, Zheng C, Dai LX. Iridium-Catalyzed Enantioselective Synthesis of Pyrrole-Annulated Medium-Sized-Ring Compounds. Angewandte Chemie (International Ed. in English). PMID 28665043 DOI: 10.1002/Anie.201705068 |
0.694 |
|
| 2016 |
Gao RD, Xu QL, Dai LX, You SL. Pd-catalyzed cascade allylic alkylation and dearomatization reactions of indoles with vinyloxirane. Organic & Biomolecular Chemistry. PMID 27511802 DOI: 10.1039/C6Ob01523A |
0.752 |
|
| 2016 |
You S, Gao RD, Xu QL, Zhang B, Gu Y, Dai LX. Palladium(0)-Catalyzed Intermolecular Allylic Dearomatization of Indoles via a Formal [4+2] Cycloaddition Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27321285 DOI: 10.1002/Chem.201602691 |
0.788 |
|
| 2016 |
You S, Liu C, Yi JC, Liang XW, Xu RQ, Dai LX. Copper(I)-Catalyzed Asymmetric Dearomatization of Indole Acetamides with 3-Indolylphenyliodonium Salts. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27171171 DOI: 10.1002/Chem.201602229 |
0.785 |
|
| 2016 |
Ye KY, Cheng Q, Zhuo CX, Dai LX, You SL. An Iridium(I) N-Heterocyclic Carbene Complex Catalyzes Asymmetric Intramolecular Allylic Amination Reactions. Angewandte Chemie (International Ed. in English). PMID 27162135 DOI: 10.1002/Anie.201603266 |
0.868 |
|
| 2016 |
Huang L, Dai LX, You SL. Enantioselective Synthesis of Indole-Annulated Medium-Sized Rings. Journal of the American Chemical Society. PMID 27093370 DOI: 10.1021/Jacs.6B02678 |
0.781 |
|
| 2015 |
Liu C, Yi JC, Zheng ZB, Tang Y, Dai LX, You SL. Enantioselective Synthesis of 3 a-Amino-Pyrroloindolines by Copper-Catalyzed Direct Asymmetric Dearomative Amination of Tryptamines. Angewandte Chemie (International Ed. in English). PMID 26603145 DOI: 10.1002/Anie.201508570 |
0.783 |
|
| 2015 |
Liu C, Yin Q, Dai LX, You SL. Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion. Chemical Communications (Cambridge, England). 51: 5971-4. PMID 25735950 DOI: 10.1039/C5Cc00780A |
0.828 |
|
| 2014 |
Ye KY, Zhang X, Dai LX, You SL. Ruthenium-catalyzed regioselective allylic trifluoromethylthiolation reaction. The Journal of Organic Chemistry. 79: 12106-10. PMID 25203498 DOI: 10.1021/Jo5019393 |
0.873 |
|
| 2014 |
Gao RD, Liu C, Dai LX, Zhang W, You SL. Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate. Organic Letters. 16: 3919-21. PMID 24992703 DOI: 10.1021/Ol501704Q |
0.759 |
|
| 2014 |
Liu C, Zhang W, Dai LX, You SL. Copper-catalyzed C-2 arylation or vinylation of indole derivatives with iodonium salts. Chemistry, An Asian Journal. 9: 2113-8. PMID 24729204 DOI: 10.1002/Asia.201402071 |
0.749 |
|
| 2014 |
Ye KY, Dai LX, You SL. Regio- and enantioselective synthesis of N-allylindoles by iridium-catalyzed allylic amination/transition-metal-catalyzed cyclization reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3040-4. PMID 24677302 DOI: 10.1002/Chem.201400026 |
0.874 |
|
| 2014 |
Ge GC, Huang XJ, Ding CH, Wan SL, Dai LX, Hou XL. A new strategy to construct a C=C-CF3 subunit via CuBr-catalyzed domino reaction of homopropargyl amines: an efficient synthesis of trifluoromethyl containing building blocks 4-trifluoromethyl-2,3-dihydro-pyrroliums. Chemical Communications (Cambridge, England). 50: 3048-51. PMID 24513681 DOI: 10.1039/C3Cc49059A |
0.654 |
|
| 2014 |
Yang XF, Li XH, Ding CH, Xu CF, Dai LX, Hou XL. Pd-catalyzed allylic alkylation of dienyl carbonates with nitromethane with high C-5 regioselectivity. Chemical Communications (Cambridge, England). 50: 484-6. PMID 24266021 DOI: 10.1039/c3cc46574h |
0.686 |
|
| 2013 |
Xu QL, Zhuo CX, Dai LX, You SL. Highly enantioselective synthesis of tetrahydrocarbolines via iridium-catalyzed intramolecular Friedel-Crafts type allylic alkylation reactions. Organic Letters. 15: 5909-11. PMID 24215126 DOI: 10.1021/Ol4027717 |
0.837 |
|
| 2013 |
Mo DL, Yuan T, Ding CH, Dai LX, Hou XL. Palladacycle-catalyzed methylenecyclopropanation of bicyclic alkenes with propiolates. The Journal of Organic Chemistry. 78: 11470-6. PMID 24128061 DOI: 10.1021/jo402024v |
0.751 |
|
| 2013 |
Wu KJ, Dai LX, You SL. Palladium(0)-catalyzed intramolecular dearomative arylation of pyrroles. Chemical Communications (Cambridge, England). 49: 8620-2. PMID 23955182 DOI: 10.1039/C3Cc44631J |
0.817 |
|
| 2013 |
Yang XF, Yu WH, Ding CH, Ding QP, Wan SL, Hou XL, Dai LX, Wang PJ. Palladium-catalyzed regio-, diastereo-, and enantioselective allylation of nitroalkanes with monosubstituted allylic substrates. The Journal of Organic Chemistry. 78: 6503-9. PMID 23741970 DOI: 10.1021/Jo400663D |
0.722 |
|
| 2012 |
Ge GC, Mo DL, Ding CH, Dai LX, Hou XL. Palladacycle-catalyzed reaction of bicyclic alkenes with terminal ynones: regiospecific synthesis of polysubstituted furans. Organic Letters. 14: 5756-9. PMID 23145937 DOI: 10.1021/ol302586m |
0.737 |
|
| 2012 |
Yang XF, Ding CH, Li XH, Huang JQ, Hou XL, Dai LX, Wang PJ. Regio- and enantioselective palladium-catalyzed allylic alkylation of nitromethane with monosubstituted allyl substrates: synthesis of (R)-rolipram and (R)-baclofen. The Journal of Organic Chemistry. 77: 8980-5. PMID 22992268 DOI: 10.1021/jo301506p |
0.655 |
|
| 2012 |
Liu C, Zhang W, Dai LX, You SL. Copper(I)-catalyzed cascade dearomatization of 2-substituted tryptophols with iodonium [corrected] salts. Organic Letters. 14: 4525-7. PMID 22891935 DOI: 10.1021/Ol301939W |
0.791 |
|
| 2012 |
Liu C, Zhang W, Dai LX, You SL. Cascade dearomatization of N-substituted tryptophols via Lewis acid-catalyzed Michael reactions. Organic & Biomolecular Chemistry. 10: 7177-83. PMID 22850826 DOI: 10.1039/C2Ob26139A |
0.797 |
|
| 2012 |
Wu KJ, Dai LX, You SL. Palladium(0)-catalyzed dearomative arylation of indoles: convenient access to spiroindolenine derivatives. Organic Letters. 14: 3772-5. PMID 22783995 DOI: 10.1021/Ol301663H |
0.807 |
|
| 2012 |
Xu QL, Dai LX, You SL. Enantioselective synthesis of tetrahydroisoquinolines via iridium-catalyzed intramolecular Friedel-Crafts-type allylic alkylation of phenols. Organic Letters. 14: 2579-81. PMID 22540154 DOI: 10.1021/Ol3008793 |
0.827 |
|
| 2012 |
Liu WB, Zhang X, Dai LX, You SL. Asymmetric N-allylation of indoles through the iridium-catalyzed allylic alkylation/oxidation of indolines. Angewandte Chemie (International Ed. in English). 51: 5183-7. PMID 22492503 DOI: 10.1002/Anie.201200649 |
0.828 |
|
| 2012 |
Ye KY, Dai LX, You SL. Enantioselective synthesis of 2,5-dihydrobenzo[b]azepine derivatives via iridium-catalyzed asymmetric allylic amination with 2-allylanilines and ring-closing-metathesis reaction. Organic & Biomolecular Chemistry. 10: 5932-9. PMID 22441972 DOI: 10.1039/C2Ob00036A |
0.878 |
|
| 2012 |
Liu WB, Zheng C, Zhuo CX, Dai LX, You SL. Iridium-catalyzed allylic alkylation reaction with N-aryl phosphoramidite ligands: scope and mechanistic studies. Journal of the American Chemical Society. 134: 4812-21. PMID 22309279 DOI: 10.1021/Ja210923K |
0.844 |
|
| 2012 |
Xu QL, Dai LX, You SL. Iridium-catalyzed enantioselective allylic alkylation of methyl 2-(4-nitrophenylsulfonyl)acetate and subsequent transformations Advanced Synthesis and Catalysis. 354: 2275-2282. DOI: 10.1002/Adsc.201200113 |
0.749 |
|
| 2012 |
He H, Ye K, Wu Q, Dai L, You S. Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives Advanced Synthesis & Catalysis. 354: 1084-1094. DOI: 10.1002/Adsc.201100809 |
0.873 |
|
| 2011 |
Ye KY, He H, Liu WB, Dai LX, Helmchen G, You SL. Iridium-catalyzed allylic vinylation and asymmetric allylic amination reactions with o-aminostyrenes. Journal of the American Chemical Society. 133: 19006-14. PMID 21995503 DOI: 10.1021/Ja2092954 |
0.872 |
|
| 2011 |
Mo DL, Ding CH, Dai LX, Hou XL. Metal-free synthesis of polysubstituted pyrroles by (diacetoxyiodo)benzene-mediated cascade reaction of 3-alkynyl amines. Chemistry, An Asian Journal. 6: 3200-4. PMID 21954112 DOI: 10.1002/asia.201100474 |
0.654 |
|
| 2011 |
Wu KJ, Li GQ, Li Y, Dai LX, You SL. N-heterocyclic carbene-catalyzed tandem aza-benzoin/Michael reactions: on site reversal of the reactivity of N-Boc imines. Chemical Communications (Cambridge, England). 47: 493-5. PMID 20953492 DOI: 10.1039/C0Cc01769H |
0.794 |
|
| 2011 |
Chen JP, Ding CH, Liu W, Hou XL, Dai LX. Palladium-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of acylsilanes with monosubstituted allyl substrates. Journal of the American Chemical Society. 132: 15493-5. PMID 20945898 DOI: 10.1021/ja106703y |
0.729 |
|
| 2010 |
Peng HM, Dai LX, You SL. Enantioselective palladium-catalyzed direct alkylation and olefination reaction of simple arenes. Angewandte Chemie (International Ed. in English). 49: 5826-8. PMID 20818771 DOI: 10.1002/Anie.201000799 |
0.824 |
|
| 2010 |
Xu QL, Liu WB, Dai LX, You SL. Iridium-catalyzed enantioselective allylic substitution of o-allyl carbamothioates. The Journal of Organic Chemistry. 75: 4615-8. PMID 20507079 DOI: 10.1021/Jo1006152 |
0.83 |
|
| 2010 |
Liu WB, He H, Dai LX, You SL. A one-pot palladium-catalyzed allylic alkylation and Wittig reaction of phosphorus ylides. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 7376-9. PMID 20486236 DOI: 10.1002/Chem.201000316 |
0.862 |
|
| 2010 |
He H, Dai LX, You SL. Intramolecular Michael addition reaction for the synthesis of benzylbutyrolactones. Organic & Biomolecular Chemistry. 8: 3207-10. PMID 20485817 DOI: 10.1039/B924770J |
0.797 |
|
| 2010 |
Zheng B, Ding C, Hou X, Dai L. Ag-Catalyzed Diastereo- and Enantioselective Synthesis of β-Substituted Tryptophans from Sulfonylindoles Organic Letters. 12: 1688-1691. PMID 20334361 DOI: 10.1021/Ol100161N |
0.673 |
|
| 2010 |
Li Q, Ding CH, Hou XL, Dai LX. Diastereo- and enantioselective synthesis of alpha,gamma-diaminobutyric acid derivatives via Cu-catalyzed asymmetric Michael reaction. Organic Letters. 12: 1080-3. PMID 20143857 DOI: 10.1021/ol100060t |
0.669 |
|
| 2010 |
Xu QL, Dai LX, You SL. Tandem Ir-catalyzed allylic substitution reaction of allyl sulfinates and isomerization. Organic Letters. 12: 800-3. PMID 20102175 DOI: 10.1021/Ol902873Q |
0.777 |
|
| 2010 |
He H, Liu WB, Dai LX, You SL. Enantioselective synthesis of 2,3-dihydro-1H-benzo[b]azepines: iridium-catalyzed tandem allylic vinylation/amination reaction. Angewandte Chemie (International Ed. in English). 49: 1496-9. PMID 20091727 DOI: 10.1002/Anie.200906638 |
0.835 |
|
| 2010 |
Zhang TK, Mo DL, Dai LX, Hou XL. Palladacycle-catalyzed highly efficient kinetic resolution of 1-hydroxy-2-aryl-1,2-dihydronaphthalenes via dehydration reaction. Organic Letters. 10: 5337-40. PMID 18980377 DOI: 10.1021/ol801946e |
0.678 |
|
| 2010 |
Fang P, Ding C, Hou X, Dai L. Palladium-catalyzed regio- and enantio-selective allylic substitution reaction of monosubstituted allyl substrates with benzyl alcohols Tetrahedron-Asymmetry. 21: 1176-1178. DOI: 10.1016/J.Tetasy.2010.03.045 |
0.572 |
|
| 2009 |
Liu WB, Zheng SC, He H, Zhao XM, Dai LX, You SL. Iridium-catalyzed regio- and enantioselective allylic alkylation of fluorobis(phenylsulfonyl)methane. Chemical Communications (Cambridge, England). 6604-6. PMID 19865664 DOI: 10.1039/B914315G |
0.808 |
|
| 2009 |
He H, Liu WB, Dai LX, You SL. Ir-catalyzed cross-coupling of styrene derivatives with allylic carbonates: free amine assisted vinyl C-H bond activation. Journal of the American Chemical Society. 131: 8346-7. PMID 19485321 DOI: 10.1021/Ja901384J |
0.846 |
|
| 2009 |
Li GQ, Dai LX, You SL. N-heterocyclic carbene catalyzed ring expansion of formylcyclopropanes: synthesis of 3,4-dihydro-alpha-pyrone derivatives. Organic Letters. 11: 1623-5. PMID 19271747 DOI: 10.1021/Ol9002898 |
0.73 |
|
| 2008 |
Wu J, Luo Z, Dai L, Hou X. Tributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate Journal of Organic Chemistry. 73: 9137-9139. PMID 18942793 DOI: 10.1021/Jo801703H |
0.734 |
|
| 2008 |
Zhang TK, Mo DL, Dai LX, Hou XL. Asymmetric ring-opening reaction of oxabicyclic alkenes with aryl boronic acids catalyzed by P-containing palladacycles. Organic Letters. 10: 3689-92. PMID 18683936 DOI: 10.1021/ol801294b |
0.728 |
|
| 2008 |
Zheng JC, Zhu CY, Sun XL, Tang Y, Dai LX. Highly diastereoselective and enantioselective formal [4 + 1] ylide annulation for the synthesis of optically active dihydrofurans. The Journal of Organic Chemistry. 73: 6909-12. PMID 18671431 DOI: 10.1021/Jo801135J |
0.493 |
|
| 2008 |
Chen DD, Hou XL, Dai LX. Unexpected transfer of tosyl group of ArCH=NTs-catalyzed by N-heterocyclic carbene. The Journal of Organic Chemistry. 73: 5578-81. PMID 18557643 DOI: 10.1021/jo800569g |
0.673 |
|
| 2008 |
Liu WB, He H, Dai LX, You SL. Ir-catalyzed regio- and enantioselective Friedel-Crafts-type allylic alkylation of indoles. Organic Letters. 10: 1815-8. PMID 18386906 DOI: 10.1021/Ol800409D |
0.817 |
|
| 2008 |
Jiang H, Sun X, Zhu C, Dai L, Tang Y. AsPh3-catalyzed ylide cyclopropanation for the synthesis of trisubstituted vinylcyclopropane derivatives Tetrahedron. 64: 5032-5035. DOI: 10.1016/J.Tet.2008.03.076 |
0.683 |
|
| 2008 |
Li G, Li Y, Dai L, You S. Enantioselective Synthesis ofcis-4-Formyl-β-lactamsviaChiral N-Heterocyclic Carbene-Catalyzed Kinetic Resolution Advanced Synthesis & Catalysis. 350: 1258-1262. DOI: 10.1002/Adsc.200800071 |
0.777 |
|
| 2007 |
Luo Z, Wu J, Hou X, Dai L. Facile preparation of α-amino ketones from oxidative ring-opening of aziridines by pyridine N-oxide Organic and Biomolecular Chemistry. 5: 3428-3430. PMID 17943199 DOI: 10.1039/B711638A |
0.612 |
|
| 2007 |
He H, Zheng XJ, Li Y, Dai LX, You SL. Ir-catalyzed regio- and enantioselective decarboxylative allylic alkylations. Organic Letters. 9: 4339-41. PMID 17854201 DOI: 10.1021/Ol7019394 |
0.763 |
|
| 2007 |
Xu ZH, Zhu SN, Sun XL, Tang Y, Dai LX. Sidearm effects in the enantioselective cyclopropanation of alkenes with aryldiazoacetates catalyzed by trisoxazoline/Cu(I). Chemical Communications (Cambridge, England). 1960-2. PMID 17695243 DOI: 10.1039/B617967C |
0.491 |
|
| 2007 |
Li GQ, Li Y, Dai LX, You SL. N-heterocyclic carbene catalyzed ring expansion of 4-formyl-beta-lactams: synthesis of succinimide derivatives. Organic Letters. 9: 3519-21. PMID 17685621 DOI: 10.1021/Ol0713537 |
0.721 |
|
| 2007 |
Li GQ, Dai LX, You SL. Thiazolium-derived N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with unactivated imines. Chemical Communications (Cambridge, England). 852-4. PMID 17308653 DOI: 10.1039/B611646A |
0.733 |
|
| 2007 |
Li CY, Wang XB, Sun XL, Tang Y, Zheng JC, Xu ZH, Zhou YG, Dai LX. Iron porphyrin-catalyzed olefination of ketenes with diazoacetate for the enantioselective synthesis of allenes. Journal of the American Chemical Society. 129: 1494-5. PMID 17283983 DOI: 10.1021/Ja068642V |
0.69 |
|
| 2007 |
You SL, Dai LX. Enantioselective palladium-catalyzed decarboxylative allylic alkylations. Angewandte Chemie (International Ed. in English). 45: 5246-8. PMID 16858703 DOI: 10.1002/Anie.200601889 |
0.834 |
|
| 2007 |
Luo Z, Hou X, Dai L. Enantioselective desymmetrization of meso-N-sulfonylaziridines with thiols Tetrahedron-Asymmetry. 18: 443-446. DOI: 10.1016/J.Tetasy.2007.02.017 |
0.534 |
|
| 2006 |
Deng XM, Cai P, Ye S, Sun XL, Liao WW, Li K, Tang Y, Wu YD, Dai LX. Enantioselective synthesis of vinylcyclopropanes and vinylepoxides mediated by camphor-derived sulfur ylides: rationale of enantioselectivity, scope, and limitation. Journal of the American Chemical Society. 128: 9730-40. PMID 16866528 DOI: 10.1021/Ja056751O |
0.519 |
|
| 2006 |
Zhang W, Ding C, Luo Z, Hou X, Dai L. Addition of benzyltrimethylsilane to imines triggered by tetrabutylammonium fluoride Tetrahedron Letters. 47: 8391-8393. DOI: 10.1016/J.Tetlet.2006.09.062 |
0.554 |
|
| 2005 |
Zheng JC, Liao WW, Sun XX, Sun XL, Tang Y, Dai LX, Deng JG. Telluronium salts mediated aziridination of chiral N-tert-butylsulfinylimines: highly stereoselective synthesis of optically active vinylaziridines. Organic Letters. 7: 5789-92. PMID 16354067 DOI: 10.1021/Ol051921N |
0.596 |
|
| 2005 |
Jiang H, Deng X, Sun X, Tang Y, Dai LX. Highly stereoselective synthesis of trisubstituted vinylcyclopropane derivatives via arsonium ylides. The Journal of Organic Chemistry. 70: 10202-5. PMID 16292874 DOI: 10.1021/Jo051782N |
0.656 |
|
| 2005 |
Yan X, Liang C, Zhang Y, Hong W, Cao B, Dai L, Hou X. Highly Enantioselective Pd‐Catalyzed Allylic Alkylations of Acyclic Ketones Angewandte Chemie. 44: 6544-6546. PMID 16173102 DOI: 10.1002/Anie.200502020 |
0.777 |
|
| 2005 |
Zheng JC, Liao WW, Tang Y, Sun XL, Dai LX. The Michael addition-elimination of ylides to alpha,beta-unsaturated imines. Highly stereoselective synthesis of vinylcyclopropanecarbaldehydes and vinylcyclopropylaziridines. Journal of the American Chemical Society. 127: 12222-3. PMID 16131190 DOI: 10.1021/Ja052228Y |
0.467 |
|
| 2004 |
Fan RH, Hou XL, Dai LX. Formation of P-ylide under neutral and metal-free conditions: transformation of aziridines and epoxides to conjugated dienes in the presence of phosphine. The Journal of Organic Chemistry. 69: 689-94. PMID 14750792 DOI: 10.1021/jo0354286 |
0.501 |
|
| 2004 |
Fan RH, Zhou YG, Zhang WX, Hou XL, Dai LX. Facile preparation of beta-fluoro amines by the reaction of aziridines with potassium fluoride dihydrate in the presence of Bu4NHSO4. The Journal of Organic Chemistry. 69: 335-8. PMID 14725444 DOI: 10.1021/Jo034895K |
0.744 |
|
| 2003 |
Tu T, Hou X, Dai L. Highly regio- and enantioselective Heck reaction of N-methoxycarbonyl-2-pyrroline with planar chiral diphosphine-oxazoline ferrocenyl ligands. Organic Letters. 5: 3651-3653. PMID 14507196 DOI: 10.1021/Ol035308K |
0.747 |
|
| 2003 |
Dai LX, Tu T, You SL, Deng WP, Hou XL. Asymmetric catalysis with chiral ferrocene ligands. Accounts of Chemical Research. 36: 659-67. PMID 12974649 DOI: 10.1021/Ar020153M |
0.813 |
|
| 2003 |
Li BF, Yuan K, Zhang MJ, Wu H, Dai LX, Wang QR, Hou XL. Highly diastereoselective strecker reaction of enolizable aliphatic sulfinimines. The Journal of Organic Chemistry. 68: 6264-7. PMID 12895059 DOI: 10.1021/jo034477f |
0.666 |
|
| 2003 |
You SL, Hou XL, Dai LX, Yu YH, Xia W. Role of planar chirality of S,N- and P,N-ferrocene ligands in palladium-catalyzed allylic substitutions. The Journal of Organic Chemistry. 67: 4684-95. PMID 12098276 DOI: 10.1021/Jo016330Z |
0.81 |
|
| 2003 |
Wang L, Kwok WH, Chan ASC, Tu T, Hou X, Dai L. Asymmetric Hydroesterification of Styrene Using Catalysts with Planar-Chiral Ferrocene Oxazoline Ligands. Cheminform. 34. DOI: 10.1016/S0957-4166(03)00455-5 |
0.54 |
|
| 2002 |
Yang XF, Zhang MJ, Hou XL, Dai LX. Stereocontrolled aziridination of imines via a sulfonium ylide route and a mechanistic study. The Journal of Organic Chemistry. 67: 8097-103. PMID 12423138 DOI: 10.1021/Jo0257389 |
0.66 |
|
| 2002 |
Hou XL, Fan RH, Dai LX. Tributylphosphine: a remarkable promoting reagent for the ring-opening reaction of aziridines. The Journal of Organic Chemistry. 67: 5295-300. PMID 12126418 |
0.672 |
|
| 2002 |
Li B, Zhang M, Hou X, Dai L. A facile synthesis of enantiopure 2-aziridinesulfinimines and their highly diastereoselective reactions with phosphite anions. Journal of Organic Chemistry. 67: 2902-2906. PMID 11975544 DOI: 10.1021/Jo016106+ |
0.729 |
|
| 2002 |
Ye S, Huang ZZ, Xia CA, Tang Y, Dai LX. A novel chiral sulfonium yilde: highly enantioselective synthesis of vinylcyclopropanes. Journal of the American Chemical Society. 124: 2432-3. PMID 11890780 DOI: 10.1021/Ja0172969 |
0.484 |
|
| 2002 |
Hou X, Luo Y, Yuan K, Dai L. Reaction of α-carbanion of imines with N-tosylimines: a facile route to β-aminoaldehydes and 1,3-diamines Journal of the Chemical Society-Perkin Transactions 1. 1487-1490. DOI: 10.1039/B200198E |
0.401 |
|
| 2001 |
You SL, Zhu XZ, Luo YM, Hou XL, Dai LX. Highly regio- and enantioselective Pd-catalyzed allylic alkylation and amination of monosubstituted allylic acetates with novel ferrocene P,N-ligands. Journal of the American Chemical Society. 123: 7471-2. PMID 11472198 DOI: 10.1021/Ja016121W |
0.736 |
|
| 2001 |
Deng WP, You SL, Hou XL, Dai LX, Yu YH, Xia W, Sun J. Importance of planar chirality in chiral catalysts with three chiral elements: the role of planar chirality in 2'-substituted 1,1'-P,N-ferrocene ligands on the enantioselectivity in Pd-catalyzed allylic substitution. Journal of the American Chemical Society. 123: 6508-19. PMID 11439037 DOI: 10.1021/Ja002657Q |
0.79 |
|
| 2001 |
You SL, Hou XL, Dai LX, Zhu XZ. Highly efficient ligands for palladium-catalyzed asymmetric alkylation of ketone enolates. Organic Letters. 3: 149-51. PMID 11430021 DOI: 10.1021/Ol0067033 |
0.772 |
|
| 2001 |
Wu X, Hou X, Dai L, Tao J, Cao B, Sun J. Synthesis of novel N,O-planar chiral [2,2]paracyclophane ligands and their application as catalysts in the addition of diethylzinc to aldehydes Tetrahedron-Asymmetry. 12: 529-532. DOI: 10.1016/S0957-4166(01)00102-1 |
0.509 |
|
| 2001 |
You S, Luo Y, Deng W, Hou X, Dai L. Palladium-catalyzed asymmetric allylic alkylations of cycloalkenyl acetates with planar chiral phosphino-ferrocene carboxylic acids Journal of Organometallic Chemistry. 637: 845-849. DOI: 10.1016/S0022-328X(01)01143-3 |
0.803 |
|
| 2001 |
You S, Hou X, Dai L. Novel ferrocene modified P,N-ligands for enantioselective palladium-catalyzed allylic substitution reactions Journal of Organometallic Chemistry. 637: 762-766. DOI: 10.1016/S0022-328X(01)00911-1 |
0.786 |
|
| 2000 |
Deng W, Hou X, Dai L, Dong X. Efficient planar chiral 2′-substituted 1,1′-P,N-ferrocene ligands for the asymmetric Heck reaction: control of enantioselectivity and configuration by planar chiral substituent Chemical Communications. 1483-1484. DOI: 10.1039/B003530K |
0.749 |
|
| 2000 |
Hou X, Wu X, Dai L, Cao B, Sun J. Novel N,S- and N,Se-planar chiral [2,2]paracyclophane ligands: synthesis and application in Pd-catalyzed allylic alkylation Chemical Communications. 1195-1196. DOI: 10.1039/B002679O |
0.595 |
|
| 2000 |
Deng W, Hou X, Dai L, Yu Y, Xia W. On the role of planar chirality: a tunable enantioselectivity in palladium-catalyzed allylic alkylation with planar chiral 1,1′-P,N-ferrocene ligands Chemical Communications. 285-286. DOI: 10.1039/A909211K |
0.62 |
|
| 1999 |
Dai L, Lin Y, Hou X, Zhou Y. Stereoselective reactions with imines Pure and Applied Chemistry. 71: 1033-1040. DOI: 10.1351/Pac199971061033 |
0.778 |
|
| 1999 |
Dai L, Hou X, Zhou Y. Stereoselective synthesis of three-membered ring compounds via ylide routes Pure and Applied Chemistry. 71: 369-376. DOI: 10.1351/Pac199971030369 |
0.783 |
|
| 1999 |
Deng W, Hou X, Dai L. The synthesis of novel chiral N,O-ferrocenyl ligands and their application in the addition of diethylzinc to aldehydes Tetrahedron-Asymmetry. 10: 4689-4693. DOI: 10.1016/S0957-4166(99)00512-1 |
0.499 |
|
| 1998 |
You S, Zhou Y, Hou X, Dai L. Enantioselective palladium catalyzed allylic substitution with chiral thioether derivatives of ferrocenyl-oxazoline and the role of planar chirality in this reaction Chemical Communications. 2765-2766. DOI: 10.1039/A808267G |
0.872 |
|
| 1996 |
Li AH, Dai LX, Hou XL, Chen MB. A Direct Route to C-Vinylaziridines: Reaction of N-Sufonylimines with Allylic Ylides under Phase-Transfer Conditions or with Preformed Ylides at Low Temperature. The Journal of Organic Chemistry. 61: 4641-4648. PMID 11667392 DOI: 10.1021/Jo952245D |
0.655 |
|
| 1996 |
Li A, Dai L, Hou X, Huang Y, Li F. Preparation of Enantiomerically Enriched (2R,3R)- or (2S,3S)-trans-2,3-Diaryloxiranes via Camphor-Derived Sulfonium Ylides. Journal of Organic Chemistry. 61: 489-493. PMID 11666965 DOI: 10.1021/Jo951442+ |
0.642 |
|
| 1996 |
Wang D, Dai L, Hou X, Zhang Y. Mg and Zn mediated allylation of imines with allyl bromide Tetrahedron Letters. 37: 4187-4188. DOI: 10.1016/0040-4039(96)00791-5 |
0.636 |
|
| Show low-probability matches. |