| Year |
Citation |
Score |
| 2024 |
Wang HC, You SL. Asymmetric Allylic Amination of Alkyl-Substituted Allylic Carbonates with Pyridones Catalyzed by the Krische Iridium Complex. Organic Letters. PMID 39331508 DOI: 10.1021/acs.orglett.4c03400 |
0.706 |
|
| 2024 |
Wu WQ, Xie PP, Wang LY, Gou BB, Lin Y, Hu LW, Zheng C, You SL, Shi H. Chiral Bis(binaphthyl) Cyclopentadienyl Ligands for Rhodium-Catalyzed Desymmetrization of Diarylmethanes via Selective Arene Coordination. Journal of the American Chemical Society. PMID 39293091 DOI: 10.1021/jacs.4c10876 |
0.662 |
|
| 2024 |
Yu X, Zheng C, You SL. Chiral Brønsted Acid-Catalyzed Intramolecular Asymmetric Dearomatization Reaction of Indoles with Cyclobutanones via Cascade Friedel-Crafts/Semipinacol Rearrangement. Journal of the American Chemical Society. PMID 39226394 DOI: 10.1021/jacs.4c09814 |
0.713 |
|
| 2024 |
Zhang WW, Feng Z, You SL, Zheng C. Electrophile-Arene Affinity: An Energy Scale for Evaluating the Thermodynamics of Electrophilic Dearomatization Reactions. The Journal of Organic Chemistry. PMID 39077910 DOI: 10.1021/acs.joc.4c01168 |
0.576 |
|
| 2024 |
You SL, Wang Y. Omentum pregnancy resulting in severe hemoperitoneum: Lessons learned from a review of the literature along with a case report. The Journal of International Medical Research. 52: 3000605241261893. PMID 39053448 DOI: 10.1177/03000605241261893 |
0.351 |
|
| 2024 |
Li W, Yu J, Wang J, Fan X, Xu X, Wang H, Xiong Y, Li X, Zhang X, Zhang Q, Qi X, Pigeon P, Gu Q, Bruno-Colmenarez J, Jaouen G, ... You SL, et al. How does ferrocene correlate with ferroptosis? Multiple approaches to explore ferrocene-appended GPX4 inhibitors as anticancer agents. Chemical Science. 15: 10477-10490. PMID 38994406 DOI: 10.1039/d4sc02002b |
0.392 |
|
| 2024 |
Li M, Huang XL, Zhang ZY, Wang Z, Wu Z, Yang H, Shen WJ, Cheng YZ, You SL. Gd(III)-Catalyzed Regio-, Diastereo-, and Enantioselective [4 + 2] Photocycloaddition of Naphthalene Derivatives. Journal of the American Chemical Society. PMID 38870424 DOI: 10.1021/jacs.4c05288 |
0.698 |
|
| 2024 |
Zheng DS, Zhao F, Gu Q, You SL. Rh(III)-catalyzed atroposelective C-H alkynylation of 1-aryl isoquinolines with hypervalent iodine-alkyne reagents. Chemical Communications (Cambridge, England). PMID 38863330 DOI: 10.1039/d4cc01785d |
0.653 |
|
| 2024 |
Zhu M, Gao YJ, Huang XL, Li M, Zheng C, You SL. Photo-induced intramolecular dearomative [5 + 4] cycloaddition of arenes for the construction of highly strained medium-sized-rings. Nature Communications. 15: 2462. PMID 38503749 DOI: 10.1038/s41467-024-46647-4 |
0.607 |
|
| 2024 |
An B, Cui H, Zheng C, Chen JL, Lan F, You SL, Zhang X. Tunable C-H functionalization and dearomatization enabled by an organic photocatalyst. Chemical Science. 15: 4114-4120. PMID 38487217 DOI: 10.1039/d4sc00120f |
0.567 |
|
| 2024 |
Shlapakov N, Kobelev A, Burykina J, Cheng YZ, You SL, Ananikov VP. Sulfur in Waste-Free Sustainable Synthesis: Advancing Carbon-Carbon Coupling Techniques. Angewandte Chemie (International Ed. in English). e202402109. PMID 38421344 DOI: 10.1002/anie.202402109 |
0.541 |
|
| 2024 |
Wu Z, Li M, Gu Q, You SL. SCpRh(III)-Catalyzed Asymmetric C-H Trifluoromethylalkylation of -Methoxybenzamides with Trifluoromethyl-α,β-Unsaturated Ketones. Organic Letters. 26: 1501-1505. PMID 38349077 DOI: 10.1021/acs.orglett.4c00177 |
0.642 |
|
| 2024 |
Song H, Li M, You SL. -Retentive Asymmetric Allylic Substitution Reactions of Aldimine Esters under Ru/Cu Dual Catalysis. Journal of the American Chemical Society. PMID 38324359 DOI: 10.1021/jacs.3c13548 |
0.663 |
|
| 2023 |
Liu CX, Zhao F, Gu Q, You SL. Enantioselective Rh(I)-Catalyzed C-H Arylation of Ferroceneformaldehydes. Acs Central Science. 9: 2036-2043. PMID 38033798 DOI: 10.1021/acscentsci.3c00748 |
0.721 |
|
| 2023 |
Yang P, Wang RX, Huang XL, Cheng YZ, You SL. Enantioselective Synthesis of Cyclobutane Derivatives via Cascade Asymmetric Allylic Etherification/[2 + 2] Photocycloaddition. Journal of the American Chemical Society. 145: 21752-21759. PMID 37768553 DOI: 10.1021/jacs.3c08792 |
0.71 |
|
| 2023 |
Liu CX, Yin SY, Zhao F, Yang H, Feng Z, Gu Q, You SL. Rhodium-Catalyzed Asymmetric C-H Functionalization Reactions. Chemical Reviews. PMID 37527349 DOI: 10.1021/acs.chemrev.3c00149 |
0.644 |
|
| 2023 |
Huang XY, Xie PP, Zou LM, Zheng C, You SL. Asymmetric Dearomatization of Indoles with Azodicarboxylates via Cascade Electrophilic Amination/Aza-Prins Cyclization/Phenonium-like Rearrangement. Journal of the American Chemical Society. PMID 37204420 DOI: 10.1021/jacs.3c02773 |
0.688 |
|
| 2023 |
Yin SY, Zhou Q, Liu CX, Gu Q, You SL. Enantioselective Synthesis of N-N Biaryl Atropisomers through Iridium(I)-Catalyzed C-H Alkylation with Acrylates. Angewandte Chemie (International Ed. in English). e202305067. PMID 37140049 DOI: 10.1002/anie.202305067 |
0.568 |
|
| 2023 |
Zhang WY, Wang HC, Wang Y, Zheng C, You SL. Enantioselective Dearomatization of Indoles via SmI-Mediated Intermolecular Reductive Coupling with Ketones. Journal of the American Chemical Society. PMID 37126434 DOI: 10.1021/jacs.3c01994 |
0.67 |
|
| 2023 |
Zhang QX, Xie JH, Gu Q, You SL. Pd-Catalyzed intermolecular asymmetric allylic dearomatization of 1-nitro-2-naphthols with MBH adducts. Chemical Communications (Cambridge, England). 59: 3590-3593. PMID 36883425 DOI: 10.1039/d3cc00568b |
0.653 |
|
| 2023 |
Zheng Y, Zhang WY, Gu Q, Zheng C, You SL. Cobalt(III)-catalyzed asymmetric ring-opening of 7-oxabenzonorbornadienes via indole C-H functionalization. Nature Communications. 14: 1094. PMID 36841798 DOI: 10.1038/s41467-023-36723-6 |
0.683 |
|
| 2023 |
Liu CX, Xie PP, Zhao F, Wang Q, Feng Z, Wang H, Zheng C, You SL. Explicit Mechanism of Rh(I)-Catalyzed Asymmetric C-H Arylation and Facile Synthesis of Planar Chiral Ferrocenophanes. Journal of the American Chemical Society. PMID 36787487 DOI: 10.1021/jacs.2c13542 |
0.663 |
|
| 2023 |
Xie JH, Hou YM, Feng Z, You SL. Stereodivergent Construction of 1,3-Chiral Centers via Tandem Asymmetric Conjugate Addition and Allylic Substitution Reaction. Angewandte Chemie (International Ed. in English). e202216396. PMID 36597878 DOI: 10.1002/anie.202216396 |
0.722 |
|
| 2022 |
Wan Q, Zheng C, Yuan YF, You SL. AgO/squaramide cocatalyzed asymmetric interrupted Barton-Zard reaction of 8-nitroimidazo[1,2-a]pyridines. Science Bulletin. 67: 1688-1695. PMID 36546048 DOI: 10.1016/j.scib.2022.07.019 |
0.697 |
|
| 2022 |
Zhang WW, Wang Q, Zhang SZ, Zheng C, You SL. (SCp)Rhodium-Catalyzed Asymmetric Satoh-Miura Reaction for Buildingup Axial Chirality: Counteranion-Directed Switching of Reaction Pathways. Angewandte Chemie (International Ed. in English). PMID 36383091 DOI: 10.1002/anie.202214460 |
0.684 |
|
| 2022 |
Zhang QX, Gu Q, You SL. Palladium(0)-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Substituted β-Naphthols with Morita-Baylis-Hillman (MBH) Adducts. Organic Letters. PMID 36264244 DOI: 10.1021/acs.orglett.2c03262 |
0.652 |
|
| 2022 |
Yang P, Wang RX, Cheng YZ, Zheng C, You SL. Iridium-Catalyzed Asymmetric Allylic Benzylation with Photogenerated Hydroxy-o-Quinodimethanes. Angewandte Chemie (International Ed. in English). PMID 36178409 DOI: 10.1002/anie.202213520 |
0.581 |
|
| 2022 |
Zhu M, Zhang X, Zheng C, You SL. Energy-Transfer-Enabled Dearomative Cycloaddition Reactions of Indoles/Pyrroles via Excited-State Aromatics. Accounts of Chemical Research. PMID 35943728 DOI: 10.1021/acs.accounts.2c00412 |
0.616 |
|
| 2022 |
Zhao K, Kohnke P, Yang Z, Cheng X, You S, Zhang L. Enantioselective Dearomative Cyclization Enabled by Asymmetric Cooperative Gold Catalysis. Angewandte Chemie (International Ed. in English). PMID 35843881 DOI: 10.1002/anie.202207518 |
0.633 |
|
| 2022 |
Yin SY, Pan C, Zhang WW, Liu CX, Zhao F, Gu Q, You SL. SCpRh(III)-Catalyzed Enantioselective Synthesis of Atropisomers by C2-Arylation of Indoles with 1-Diazonaphthoquinones. Organic Letters. PMID 35575309 DOI: 10.1021/acs.orglett.2c01141 |
0.67 |
|
| 2022 |
Zou LM, Huang XY, Zheng C, Cheng YZ, You SL. Chiral Brønsted Acid-Catalyzed Intramolecular Asymmetric Allylic Alkylation of Indoles with Primary Alcohols. Organic Letters. PMID 35533379 DOI: 10.1021/acs.orglett.2c01253 |
0.626 |
|
| 2022 |
Ding L, Song H, Zheng C, You SL. Enantioselective Synthesis of Medium-Sized-Ring Lactones via Iridium-Catalyzed -Retentive Asymmetric Allylic Substitution Reaction. Journal of the American Chemical Society. 144: 4770-4775. PMID 35266702 DOI: 10.1021/jacs.2c01103 |
0.679 |
|
| 2022 |
Coppola GA, Pillitteri S, Van der Eycken EV, You SL, Sharma UK. Multicomponent reactions and photo/electrochemistry join forces: atom economy meets energy efficiency. Chemical Society Reviews. 51: 2313-2382. PMID 35244107 DOI: 10.1039/d1cs00510c |
0.6 |
|
| 2022 |
Liu XJ, Zhang WY, Zheng C, You SL. Iridium-Catalyzed Asymmetric Allylic Substitution of Methyl Azaarenes. Angewandte Chemie (International Ed. in English). e202200164. PMID 35238122 DOI: 10.1002/anie.202200164 |
0.713 |
|
| 2022 |
Cheng YZ, Feng Z, Zhang X, You SL. Visible-light induced dearomatization reactions. Chemical Society Reviews. 51: 2145-2170. PMID 35212320 DOI: 10.1039/c9cs00311h |
0.558 |
|
| 2022 |
Nie YH, Komatsuda M, Yang P, Zheng C, Yamaguchi J, You SL. Pd-Catalyzed Asymmetric Dearomative Arylation of Indoles via a Desymmetrization Strategy. Organic Letters. PMID 35156828 DOI: 10.1021/acs.orglett.2c00129 |
0.678 |
|
| 2022 |
Zhang WW, Liu CX, Yang P, Zhang SZ, Gu Q, You SL. Rhodium-Catalyzed Atroposelective C-H/C-H Cross-Coupling Reaction between 1-Aryl Isoquinoline Derivatives and Indolizines. Organic Letters. PMID 34985290 DOI: 10.1021/acs.orglett.1c04002 |
0.605 |
|
| 2021 |
Pan C, Yin SY, Gu Q, You SL. CpM(iii)-catalyzed enantioselective C-H functionalization through migratory insertion of metal-carbenes/nitrenes. Organic & Biomolecular Chemistry. 19: 7264-7275. PMID 34612356 DOI: 10.1039/d1ob01248g |
0.631 |
|
| 2021 |
Zhang SS, Xue J, Gu Q, Jiang X, You SL. Dearomatization reaction of β-naphthols with disulfurating reagents. Organic & Biomolecular Chemistry. PMID 34581384 DOI: 10.1039/d1ob01731d |
0.62 |
|
| 2021 |
Liu CX, Zhang WW, Yin SY, Gu Q, You SL. Synthesis of Atropisomers by Transition-Metal-Catalyzed Asymmetric C-H Functionalization Reactions. Journal of the American Chemical Society. PMID 34432467 DOI: 10.1021/jacs.1c07635 |
0.621 |
|
| 2021 |
Zhu M, Huang XL, Sun S, Zheng C, You SL. Visible-Light-Induced Dearomatization of Indoles/Pyrroles with Vinylcyclopropanes: Expedient Synthesis of Structurally Diverse Polycyclic Indolines/Pyrrolines. Journal of the American Chemical Society. PMID 34398603 DOI: 10.1021/jacs.1c07082 |
0.601 |
|
| 2021 |
Xie JH, Zheng C, You S. Palladium-Catalyzed Dearomative Methoxyallylation of 3-Nitroindoles with Allyl Carbonates. Angewandte Chemie (International Ed. in English). PMID 34273125 DOI: 10.1002/anie.202107139 |
0.621 |
|
| 2021 |
Wan Q, Xie JH, Zheng C, Yuan YF, You S, You SL. Ag-Catalyzed Asymmetric Dearomatization of Electron-deficient Heteroarenes via Interrupted Barton-Zard Reaction. Angewandte Chemie (International Ed. in English). PMID 34196074 DOI: 10.1002/anie.202107767 |
0.684 |
|
| 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 |
0.717 |
|
| 2021 |
Pan CQ, Yin SY, Wang SB, Gu Q, You S. Oxygen-linked Cyclopentadienyl Rh(III) Complexes-Catalyzed Asymmetric C-H Arylation of Benzo[h]quinolines with 1-Diazonaphthoquinones. Angewandte Chemie (International Ed. in English). PMID 33856719 DOI: 10.1002/anie.202103638 |
0.63 |
|
| 2021 |
Zheng C, You SL. Advances in Catalytic Asymmetric Dearomatization. Acs Central Science. 7: 432-444. PMID 33791426 DOI: 10.1021/acscentsci.0c01651 |
0.651 |
|
| 2021 |
Lin Z, Xue Y, Liang X, Wang J, Lin S, Tao J, You SL, Liu W. Oxidative Indole Dearomatization for Asymmetric Furoindoline Synthesis by a Flavin-Dependent Monooxygenase Involved in the Biosynthesis of Bicyclic Thiopeptide Thiostrepton. Angewandte Chemie (International Ed. in English). PMID 33496012 DOI: 10.1002/anie.202013174 |
0.629 |
|
| 2021 |
Jiang R, Ding L, Zheng C, You SL. Iridium-catalyzed -retentive asymmetric allylic substitution reactions. Science (New York, N.Y.). 371: 380-386. PMID 33479149 DOI: 10.1126/science.abd6095 |
0.715 |
|
| 2021 |
You S, Zhu M, Zhang X, Zheng C. Visible-light-induced Intramolecular Double Dearomative Cycloaddition of Arenes. Angewandte Chemie (International Ed. in English). PMID 33449427 DOI: 10.1002/anie.202016899 |
0.586 |
|
| 2020 |
Wang Q, Liu CX, Gu Q, You SL. Chiral CpRh complexes for C-H functionalization reactions. Science Bulletin. 66: 210-213. PMID 36654324 DOI: 10.1016/j.scib.2020.09.035 |
0.587 |
|
| 2020 |
Wang Q, Zhang WW, Zheng C, Gu Q, You SL. Enantioselective Synthesis of Azoniahelicenes by Rh-Catalyzed C-H Annulation with Alkynes. Journal of the American Chemical Society. PMID 33356232 DOI: 10.1021/jacs.0c11735 |
0.685 |
|
| 2020 |
Huang XL, Cheng YZ, Zhang X, You SL. Photoredox-Catalyzed Intermolecular Hydroalkylative Dearomatization of Electron-Deficient Indole Derivatives. Organic Letters. PMID 33295778 DOI: 10.1021/acs.orglett.0c03759 |
0.523 |
|
| 2020 |
Wang Y, Zhang WY, Xie JH, Yu ZL, Tan JH, Zheng C, Hou XL, You SL. Enantioselective Desymmetrization of Bisphenol Derivatives via Ir-Catalyzed Allylic Dearomatization. Journal of the American Chemical Society. PMID 33140959 DOI: 10.1021/jacs.0c09638 |
0.715 |
|
| 2020 |
Sharma UK, Ranjan P, Van der Eycken EV, You SL. Sequential and direct multicomponent reaction (MCR)-based dearomatization strategies. Chemical Society Reviews. PMID 33079105 DOI: 10.1039/d0cs00128g |
0.533 |
|
| 2020 |
Yang P, Zheng C, Nie YH, You SL. Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes. Chemical Science. 11: 6830-6835. PMID 33033598 DOI: 10.1039/D0Sc02816A |
0.721 |
|
| 2020 |
Wang Q, Zhang WW, Song H, Wang J, Zheng C, Gu Q, You SL. Rhodium-Catalyzed Atroposelective Oxidative C-H/C-H Cross Coupling Reaction of 1-Aryl Isoquinoline Derivatives with Electron-Rich Heteroarenes. Journal of the American Chemical Society. PMID 32865413 DOI: 10.1021/Jacs.0C08205 |
0.669 |
|
| 2020 |
Tu HF, Yang P, Lin ZH, Zheng C, You SL. Publisher Correction: Time-dependent enantiodivergent synthesis via sequential kinetic resolution. Nature Chemistry. PMID 32782405 DOI: 10.1038/S41557-020-0546-9 |
0.528 |
|
| 2020 |
Ding L, Wu WT, Zhang L, You SL. Construction of Spironaphthalenones via Gold-Catalyzed Intramolecular Dearomatization Reaction of β-Naphthol Derivatives. Organic Letters. PMID 32644806 DOI: 10.1021/Acs.Orglett.0C01945 |
0.642 |
|
| 2020 |
You S, Cheng YZ, Huang XL, Zhuang WH, Zhao QR, Zhang X, Mei TS. Intermolecular Dearomatization of Naphthalene Derivatives via a Photoredox-Catalyzed 1,2-Hydroalkylation. Angewandte Chemie (International Ed. in English). PMID 32618055 DOI: 10.1002/Anie.202008358 |
0.68 |
|
| 2020 |
Tu HF, Yang P, Lin ZH, Zheng C, You SL. Time-dependent enantiodivergent synthesis via sequential kinetic resolution. Nature Chemistry. PMID 32601409 DOI: 10.1038/S41557-020-0489-1 |
0.708 |
|
| 2020 |
Shao W, Xu-Xu QF, You S. Highly Diastereoselective Synthesis of Polycyclic Indolines through Formal [4+2] Propargylic Cycloaddition of Indoles with Ethynyl Benzoxazinanones. Chemistry, An Asian Journal. PMID 32578956 DOI: 10.1002/Asia.202000640 |
0.627 |
|
| 2020 |
Gao PS, Weng XJ, Wang ZH, Zheng C, Sun B, Chen ZH, You SL, Mei TS. Cu(II)/TEMPO-Catalyzed Enantioselective C(sp3)-H Alkynylation of Tertiary Cyclic Amines via Shono-type Oxidation. Angewandte Chemie (International Ed. in English). PMID 32394631 DOI: 10.1002/Anie.202005099 |
0.599 |
|
| 2020 |
Zheng C, You SL. Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet-Spengler-type Reactions and Beyond. Accounts of Chemical Research. PMID 32275392 DOI: 10.1021/Acs.Accounts.0C00074 |
0.712 |
|
| 2020 |
Cui WJ, Wu ZJ, Gu Q, You SL. Divergent Synthesis of Tunable Cyclopentadienyl Ligands and Their Application in Rh-catalyzed Enantioselective Synthesis of Isoindolinone. Journal of the American Chemical Society. PMID 32259425 DOI: 10.1021/Jacs.0C02813 |
0.744 |
|
| 2020 |
Zhang HJ, Gu Q, You SL. Ni-Catalyzed Allylic Dearomatization Reaction of β-Naphthols with Allylic Alcohols. Organic Letters. PMID 32243173 DOI: 10.1021/Acs.Orglett.0C01109 |
0.635 |
|
| 2020 |
Rossi-Ashton JA, Clarke AK, Donald JR, Zheng C, Taylor RJK, Unsworth WP, You SL. Iridium Catalyzed Enantioselective Intermolecular Indole C2-Allylation. Angewandte Chemie (International Ed. in English). PMID 32091146 DOI: 10.1002/Anie.202001956 |
0.662 |
|
| 2020 |
Xu-Xu QF, Zhang X, You SL. Enantioselective Synthesis of 4-Allyl Tetrahydroquinolines via Copper(I) Hydride-Catalyzed Hydroallylation of 1,2-Dihydroquinolines. Organic Letters. PMID 32009411 DOI: 10.1021/Acs.Orglett.0C00113 |
0.683 |
|
| 2020 |
Xu-Xu Q, Yang P, Zhang X, You S. Enantioselective Synthesis of 4-Silyl-1,2,3,4-tetrahydroquinolines via Copper(I) Hydride Catalyzed Asymmetric Hydrosilylation of 1,2-Dihydroquinolines Synlett. DOI: 10.1055/S-0040-1707134 |
0.663 |
|
| 2020 |
Xu R, Yang P, Zheng C, You S. Pd‐Catalyzed
Asymmetric Intramolecular Arylative Dearomatization of
para
‐Aminophenols
† Chinese Journal of Chemistry. 38: 683-689. DOI: 10.1002/Cjoc.202000109 |
0.728 |
|
| 2020 |
Yang P, Xu R, Zheng C, You S. Pd‐Catalyzed Dearomatization of Indole Derivatives
via
Intermolecular Heck Reactions
† Chinese Journal of Chemistry. 38: 235-241. DOI: 10.1002/Cjoc.201900509 |
0.691 |
|
| 2019 |
Xia ZL, Xu-Xu QF, Zheng C, You SL. Chiral phosphoric acid-catalyzed asymmetric dearomatization reactions. Chemical Society Reviews. PMID 31829319 DOI: 10.1039/C8Cs00436F |
0.705 |
|
| 2019 |
Wu WT, Ding L, Zhang L, You SL. Gold-Catalyzed Intramolecular Dearomatization Reactions of Indoles for the Synthesis of Spiroindolenines and Spiroindolines. Organic Letters. PMID 31789039 DOI: 10.1021/Acs.Orglett.9B03988 |
0.743 |
|
| 2019 |
Zhang HJ, Gu Q, You SL. Ni-Catalyzed Intermolecular Allylic Dearomatization Reaction of Tryptophols and Tryptamines. Organic Letters. PMID 31714790 DOI: 10.1021/Acs.Orglett.9B03633 |
0.717 |
|
| 2019 |
You S, Liu XJ, Jin S, Zhang WY, Liu QQ, Zheng C. Sequence-Dependent Stereodivergent Allylic Alkylation/Fluorination Reaction of Acyclic Ketones. Angewandte Chemie (International Ed. in English). PMID 31693789 DOI: 10.1002/Anie.201912882 |
0.691 |
|
| 2019 |
You S, Cheng YZ, Zhao QR, Zhang X, You SL. Asymmetric Dearomatization of Indole Derivatives with N-Hydroxycarbamates Enabled by Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 31587423 DOI: 10.1002/Anie.201911144 |
0.731 |
|
| 2019 |
Cai ZJ, Liu CX, Wang Q, Gu Q, You SL. Thioketone-directed rhodium(I) catalyzed enantioselective C-H bond arylation of ferrocenes. Nature Communications. 10: 4168. PMID 31519893 DOI: 10.1038/S41467-019-12181-X |
0.7 |
|
| 2019 |
Xiang JC, Wu ZJ, Gu Q, You SL. Palladium-Catalyzed C-H Diarylation of Ferrocenecarboxylic Acids with Aryl Iodides. The Journal of Organic Chemistry. PMID 31342746 DOI: 10.1021/Acs.Joc.9B01503 |
0.661 |
|
| 2019 |
Zhai Y, You SL, Ma S. Palladium-catalyzed intermolecular allenylation reactions of 2,3-disubstituted indoles and allenyl carbonate. Organic & Biomolecular Chemistry. PMID 31328763 DOI: 10.1039/C9Ob01435G |
0.696 |
|
| 2019 |
Tang SB, Tu HF, Zhang X, You SL. Rhodium-Catalyzed Asymmetric Allylic Dearomatization of β-Naphthols: Enantioselective Control of Prochiral Nucleophiles. Organic Letters. PMID 31318562 DOI: 10.1021/Acs.Orglett.9B02285 |
0.688 |
|
| 2019 |
Xia ZL, Zheng C, Xu RQ, You SL. Chiral phosphoric acid catalyzed aminative dearomatization of α-naphthols/Michael addition sequence. Nature Communications. 10: 3150. PMID 31316064 DOI: 10.1038/S41467-019-11109-9 |
0.739 |
|
| 2019 |
Xu-Xu QF, Zhang X, You SL. Enantioselective Synthesis of 4-Aminotetrahydroquinolines via 1,2-Reductive Dearomatization of Quinolines and Copper(I) Hydride-Catalyzed Asymmetric Hydroamination. Organic Letters. PMID 31247783 DOI: 10.1021/Acs.Orglett.9B02034 |
0.666 |
|
| 2019 |
Wang Q, Cai ZJ, Liu CX, Gu Q, You SL. Rhodium-Catalyzed Atroposelective C-H Arylation: Efficient Synthesis of Axially Chiral Heterobiaryls. Journal of the American Chemical Society. PMID 31184139 DOI: 10.1021/Jacs.9B03862 |
0.713 |
|
| 2019 |
You S, Liu XJ, Zheng C, Yang YH, Jin S. Iridium-Catalyzed Asymmetric Allylic Aromatization Reaction. Angewandte Chemie (International Ed. in English). PMID 31081989 DOI: 10.1002/Anie.201904156 |
0.743 |
|
| 2019 |
Zhang HJ, Yang ZP, Gu Q, You SL. Tandem Pd-Catalyzed Intermolecular Allylic Alkylation/Allylic Dearomatization Reaction of Benzoylmethyl pyridines, Pyrazines, and Quinolines. Organic Letters. PMID 31001983 DOI: 10.1021/Acs.Orglett.9B01060 |
0.708 |
|
| 2019 |
Aspuru-Guzik A, Baik MH, Balasubramanian S, Banerjee R, Bart S, Borduas-Dedekind N, Chang S, Chen P, Corminboeuf C, Coudert FX, Cronin L, Crudden C, Cuk T, Doyle AG, Fan C, ... You SL, et al. Charting a course for chemistry. Nature Chemistry. 11: 286-294. PMID 30903035 DOI: 10.1038/S41557-019-0236-7 |
0.403 |
|
| 2019 |
Zheng C, You SL. Catalytic asymmetric dearomatization (CADA) reaction-enabled total synthesis of indole-based natural products. Natural Product Reports. PMID 30839047 DOI: 10.1039/C8Np00098K |
0.695 |
|
| 2019 |
You S, Cheng Q, Xie JH, Weng YC. Pd-Catalyzed Dearomatization of Anthranils with Vinylcyclopropanes via [4+3] Cyclization Reaction. Angewandte Chemie (International Ed. in English). PMID 30811778 DOI: 10.1002/Anie.201901251 |
0.711 |
|
| 2019 |
Ding L, Gao RD, You S. Palladium(0)-Catalyzed Intermolecular Asymmetric Cascade Dearomatization Reaction of Indoles with Propargyl Carbonate. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30694590 DOI: 10.1002/Chem.201900425 |
0.682 |
|
| 2019 |
Wang Y, Zhang WY, You SL. Ketones and Aldehydes as O-Nucleophiles in Iridium-Catalyzed Intramolecular Asymmetric Allylic Substitution Reaction. Journal of the American Chemical Society. PMID 30689947 DOI: 10.1021/Jacs.8B13182 |
0.748 |
|
| 2019 |
Zhu M, Zheng C, Zhang X, You SL. Synthesis of Cyclobutane-Fused Angular Tetracyclic Spiroindolines via Visible-Light-Promoted Intramolecular Dearomatization of Indole Derivatives. Journal of the American Chemical Society. PMID 30653315 DOI: 10.1021/Jacs.8B12965 |
0.617 |
|
| 2019 |
Zhang H, Gu Q, You S. Recent Advances in Ni-Catalyzed Allylic Substitution Reactions Chinese Journal of Organic Chemistry. 39: 15. DOI: 10.6023/Cjoc201809037 |
0.682 |
|
| 2019 |
Wang Q, Gu Q, You S. Recent Progress on Transition-Metal-Catalyzed Asymmetric C-H Bond Functionalization for the Synthesis of Biaryl Atropisomers Acta Chimica Sinica. 77: 690. DOI: 10.6023/A19060222 |
0.569 |
|
| 2019 |
Zheng D, Zhao Z, Gu Q, You S. Ir-Catalyzed Intermolecular Asymmetric Allylic Alkylationof β‑Tetralones Organometallics. 38: 3996-4002. DOI: 10.1021/Acs.Organomet.9B00416 |
0.574 |
|
| 2019 |
Zhang M, Wang D, Xie M, Qu G, Guo H, You S. Cu-catalyzed Asymmetric Dearomative [3 + 2] Cycloaddition Reaction of Benzazoles with Aminocyclopropanes Chem. 5: 156-167. DOI: 10.1016/J.Chempr.2018.10.003 |
0.699 |
|
| 2019 |
Yi J, Wu Z, You S. Rh‐Catalyzed Aminative Dearomatization of Naphthols with Hydroxylamine‐O‐Sulfonic Acid (HOSA) European Journal of Organic Chemistry. 2019: 5736-5739. DOI: 10.1002/Ejoc.201900917 |
0.527 |
|
| 2019 |
Yi J, Wu Z, You S. Copper‐Catalyzed Oxidative Dearomatization of 2‐Naphthols via Etherification Chinese Journal of Chemistry. 37: 903-908. DOI: 10.1002/Cjoc.201900242 |
0.645 |
|
| 2018 |
Cheng YZ, Zhang X, You SL. Visible-light-mediated photocatalysis as a new tool for catalytic asymmetric dearomatization (CADA) reactions. Science Bulletin. 63: 809-811. PMID 36658957 DOI: 10.1016/j.scib.2018.06.006 |
0.569 |
|
| 2018 |
Cai ZJ, Liu CX, Gu Q, Zheng C, You S. Pd(II)-Catalyzed Regio- and Enantioselective Oxidative C-H/C-H Cross-Coupling Reaction between Ferrocenes and Azoles. Angewandte Chemie (International Ed. in English). PMID 30589183 DOI: 10.1002/Anie.201813887 |
0.646 |
|
| 2018 |
Cheng Q, Tu HF, Zheng C, Qu JP, Helmchen G, You SL. Iridium-Catalyzed Asymmetric Allylic Substitution Reactions. Chemical Reviews. PMID 30582688 DOI: 10.1021/Acs.Chemrev.8B00506 |
0.728 |
|
| 2018 |
You S, Xia ZL, Zheng C, Liang XW, Cai Y. Manipulation of Spiroindolenine Intermediates for the Enantioselective Synthesis of 3-(Indol-3-yl)pyrrolidines. Angewandte Chemie (International Ed. in English). PMID 30508307 DOI: 10.1002/Anie.201812344 |
0.729 |
|
| 2018 |
Yang P, You SL. Palladium-Catalyzed Asymmetric Intramolecular Dearomative Heck Reaction of Pyrrole Derivatives. Organic Letters. PMID 30411626 DOI: 10.1021/Acs.Orglett.8B03425 |
0.71 |
|
| 2018 |
Yi JC, Tu HF, You SL. Rh-Catalyzed aminative dearomatization of 2-naphthols. Organic & Biomolecular Chemistry. PMID 30406793 DOI: 10.1039/C8Ob02592D |
0.7 |
|
| 2018 |
You S, Yang ZP, Jiang R, Wu QF, Huang L, Zheng C. Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Benzene Derivatives. Angewandte Chemie (International Ed. in English). PMID 30328238 DOI: 10.1002/Anie.201810900 |
0.735 |
|
| 2018 |
Zhang X, You SL. THQphos in Ir-catalyzed Asymmetric Allylic Substitution Reactions. Chimia. 72: 589-594. PMID 30257732 DOI: 10.2533/chimia.2018.589 |
0.688 |
|
| 2018 |
You S, Xu-Xu QF, Liu QQ, Zhang X. Copper-Catalyzed Ring Opening of Benzofurans and Enantioselective Hydroamination Cascade. Angewandte Chemie (International Ed. in English). PMID 30251383 DOI: 10.1002/Anie.201809003 |
0.674 |
|
| 2018 |
Ding L, You SL. Palladium(0)-Catalyzed Intermolecular Cascade Dearomatization Reaction of β-Naphthol Derivatives with Propargyl Carbonates. Organic Letters. PMID 30234306 DOI: 10.1021/Acs.Orglett.8B02681 |
0.647 |
|
| 2018 |
You S, Wang Q, Gu Q. Enantioselective Carbonyl Catalysis Enabled by Chiral Aldehydes. Angewandte Chemie (International Ed. in English). PMID 30216640 DOI: 10.1002/Anie.201808700 |
0.692 |
|
| 2018 |
Cai Y, Gu Q, You SL. Chemoselective N-H functionalization of indole derivatives via the Reissert-type reaction catalyzed by a chiral phosphoric acid. Organic & Biomolecular Chemistry. PMID 30101274 DOI: 10.1039/C8Ob01863D |
0.725 |
|
| 2018 |
Zhu M, Zhou K, Zhang X, You SL. Visible-Light-Promoted Cascade Alkene Trifluoromethylation and Dearomatization of Indole Derivatives via Intermolecular Charge Transfer. Organic Letters. PMID 29985618 DOI: 10.1021/Acs.Orglett.8B01899 |
0.609 |
|
| 2018 |
You S, Cheng YZ, Zhou K, Zhu M, Li LA, Zhang X. Visible-Light Promoted Intermolecular Oxidative Dearomatization of β-Naphthols with N-Hydroxycarbamates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29932260 DOI: 10.1002/Chem.201803149 |
0.573 |
|
| 2018 |
Tang SB, Zhang X, Tu HF, You SL. Regio- and Enantioselective Rhodium-Catalyzed Allylic Alkylation of Racemic Allylic Alcohols with 1,3-Diketones. Journal of the American Chemical Society. PMID 29799203 DOI: 10.1021/Jacs.8B05126 |
0.676 |
|
| 2018 |
Cheng R, Li B, Wu J, Zhang J, Qiu Z, Tang W, You SL, Tang Y, Xie Z. Enantioselective Synthesis of Chiral-at-Cage o-Carboranes via Pd-Catalyzed Asymmetric B-H Substitution. Journal of the American Chemical Society. PMID 29575894 DOI: 10.1021/Jacs.8B01754 |
0.703 |
|
| 2018 |
You S, Shao W, Wang Y, Yang ZP, Zhang X. Efficient Synthesis of N-Alkylated 4-Pyridones by Copper-Catalyzed Intermolecular Asymmetric Propargylic Amination. Chemistry, An Asian Journal. PMID 29542867 DOI: 10.1002/Asia.201800373 |
0.677 |
|
| 2018 |
Yang ZP, Jiang R, Zheng C, You SL. Iridium-Catalyzed Intramolecular Asymmetric Allylic Alkylation of Hydroxyquinolines: Simultaneous Weakening the Aromaticity of Two Consecutive Aromatic Rings. Journal of the American Chemical Society. PMID 29431997 DOI: 10.1021/Jacs.8B00136 |
0.742 |
|
| 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 |
0.735 |
|
| 2018 |
You S, Cheng Q, Zhang F, Cai Y, Guo YL. Stereodivergent Synthesis of Tetrahydrofuroindoles via Pd-Catalyzed Asymmetric Dearomative Formal [3+2] Cycloaddition Reactions. Angewandte Chemie (International Ed. in English). PMID 29330914 DOI: 10.1002/Anie.201711873 |
0.721 |
|
| 2018 |
You S, Xia ZL, Zheng C, Wang SG. Catalytic Asymmetric Dearomatization of Indolyl Dihydropyridines via Enamine Isomerization/Spirocyclization/Transfer Hydrogenation Sequence. Angewandte Chemie (International Ed. in English). PMID 29327453 DOI: 10.1002/Anie.201712435 |
0.726 |
|
| 2018 |
Gao R, Zhai Y, You S, Ma S. Palladium-catalyzed intermolecular dearomatic allenylation of hydrocycloalk[b]indoles with 2,3-allenyl carbonates Organic Chemistry Frontiers. 5: 1664-1669. DOI: 10.1039/C8Qo00163D |
0.565 |
|
| 2018 |
Tu H, Zhang X, Zheng C, Zhu M, You S. Enantioselective dearomative prenylation of indole derivatives Nature Catalysis. 1: 601-608. DOI: 10.1038/s41929-018-0111-8 |
0.41 |
|
| 2018 |
Bao C, Zheng D, Zhang X, You S. Iridium/N-Heterocyclic Carbene Complex-Catalyzed Intermolecular Allylic Alkylation Reaction Organometallics. 37: 4763-4772. DOI: 10.1021/Acs.Organomet.8B00762 |
0.732 |
|
| 2018 |
Cheng Y, Zhang X, You S. Visible-light-mediated photocatalysis as a new tool for catalytic asymmetric dearomatization (CADA) reactions Chinese Science Bulletin. 63: 809-811. DOI: 10.1016/J.Scib.2018.06.006 |
0.618 |
|
| 2018 |
Wang S, Gu Q, You S. Cp*Co(III)-catalyzed ortho C-H amidation of 2-pyridinyl ferrocenes with 1,4,2-dioxazol-5-ones Journal of Catalysis. 361: 393-397. DOI: 10.1016/J.Jcat.2018.03.007 |
0.677 |
|
| 2018 |
Zheng C, Xia Z, You S. Unified Mechanistic Understandings of Pictet-Spengler Reactions Chem. 4: 1952-1966. DOI: 10.1016/J.Chempr.2018.06.006 |
0.658 |
|
| 2018 |
Liang X, Chen X, Zhang Z, You S. Catalytic asymmetric brominative dearomatization reaction of benzofurans Chinese Chemical Letters. 29: 1212-1214. DOI: 10.1016/J.Cclet.2018.01.039 |
0.733 |
|
| 2018 |
Liang X, Cai Y, You S. Asymmetric Fluorinative Dearomatization of Tryptophol Derivatives by Chiral Anion Phase-Transfer Catalysis Chinese Journal of Chemistry. 36: 925-928. DOI: 10.1002/Cjoc.201800319 |
0.572 |
|
| 2017 |
You S, Cai ZJ, Liu CX, Gu Q. Thioketone Directed Palladium(II)-Catalyzed C-H Arylation of Ferrocenes with Aryl Boronic Acids. Angewandte Chemie (International Ed. in English). PMID 29226499 DOI: 10.1002/Anie.201711451 |
0.672 |
|
| 2017 |
You S, Wang Y, Zheng C. Ir-Catalyzed Asymmetric Allylic Dearomatization via a Desymmetrization Strategy. Angewandte Chemie (International Ed. in English). PMID 28980373 DOI: 10.1002/Anie.201708419 |
0.712 |
|
| 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 |
0.608 |
|
| 2017 |
You S, Zhao ZL, Gu Q, Wu XY. Anilines as C-Nucleophiles in Ir-Catalyzed Intramolecular Asymmetric Allylic Substitution Reactions. Chemistry, An Asian Journal. PMID 28846203 DOI: 10.1002/Asia.201701192 |
0.748 |
|
| 2017 |
You S, Shao W. Highly Diastereo- and Enantioselective Synthesis of Tetrahydro-5H-Indolo[2,3-b]quinolines via Copper-Catalyzed Propargylic Dearomatization of Indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28748548 DOI: 10.1002/Chem.201703443 |
0.644 |
|
| 2017 |
Glavač D, Zheng C, Dokli I, You SL, Gredičak M. Chiral Brønsted Acid-Catalyzed Enantioselective aza-Friedel-Crafts Reaction of Cyclic α-Diaryl N-Acyl Imines With Indoles. The Journal of Organic Chemistry. PMID 28742360 DOI: 10.1021/Acs.Joc.7B01420 |
0.698 |
|
| 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 |
0.617 |
|
| 2017 |
Xu RQ, Yang P, You SL. Pd(0)-Catalyzed intramolecular arylative dearomatization of β-naphthols. Chemical Communications (Cambridge, England). PMID 28634612 DOI: 10.1039/C7Cc04022A |
0.697 |
|
| 2017 |
Xu RQ, Gu Q, You SL. Construction of the Benzomesembrine Skeleton: Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of α-Naphthols and Subsequent Aza-Michael Reaction. Angewandte Chemie (International Ed. in English). PMID 28510365 DOI: 10.1002/Anie.201703674 |
0.728 |
|
| 2017 |
Liang XW, Liu C, Zhang W, You SL. Asymmetric fluorinative dearomatization of tryptamine derivatives. Chemical Communications (Cambridge, England). PMID 28466889 DOI: 10.1039/C7Cc02419C |
0.698 |
|
| 2017 |
Wang SB, Gu Q, You SL. Rh(III)-Catalyzed C-H Alkynylation of Ferrocenes with Hypervalent Iodine Reagents. The Journal of Organic Chemistry. PMID 28466643 DOI: 10.1021/Acs.Joc.7B00775 |
0.664 |
|
| 2017 |
You S, Wang SG, Xia ZL, Xu RQ, Liu XJ, Zheng C. Construction of Chiral Tetrahydro-β-Carbolines through Asymmetric Pictet-Spengler Reaction of Indolyl Dihydropyridines. Angewandte Chemie (International Ed. in English). PMID 28466512 DOI: 10.1002/Anie.201703178 |
0.718 |
|
| 2017 |
Zheng J, Wang SB, Zheng C, You SL. Asymmetric Synthesis of Spiropyrazolones by Rhodium-Catalyzed C(sp(2) )-H Functionalization/Annulation Reactions. Angewandte Chemie (International Ed. in English). PMID 28328101 DOI: 10.1002/Anie.201700021 |
0.737 |
|
| 2017 |
Liu XJ, You SL. Enantioselective Iridium-Catalyzed Allylic Substitution with 2-Methylpyridines. Angewandte Chemie (International Ed. in English). PMID 28266102 DOI: 10.1002/Anie.201700433 |
0.704 |
|
| 2017 |
Li GT, Li ZK, Gu Q, You SL. Asymmetric Synthesis of 4-Aryl-3,4-dihydrocoumarins by N-Heterocyclic Carbene Catalyzed Annulation of Phenols with Enals. Organic Letters. PMID 28233489 DOI: 10.1021/Acs.Orglett.7B00088 |
0.723 |
|
| 2017 |
Zhou Y, Xia ZL, Gu Q, You SL. Chiral Phosphoric Acid Catalyzed Intramolecular Dearomative Michael Addition of Indoles to Enones. Organic Letters. PMID 28145710 DOI: 10.1021/Acs.Orglett.6B03610 |
0.733 |
|
| 2017 |
Gao DW, Gu Q, Zheng C, You SL. Synthesis of Planar Chiral Ferrocenes via Transition-Metal-Catalyzed Direct C-H Bond Functionalization. Accounts of Chemical Research. PMID 28121428 DOI: 10.1021/Acs.Accounts.6B00573 |
0.85 |
|
| 2017 |
Yang ZP, Zheng C, Huang L, Qian C, You SL. Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Benzoxazoles, Benzothiazoles, and Benzimidazoles. Angewandte Chemie (International Ed. in English). PMID 28074594 DOI: 10.1002/Anie.201611056 |
0.735 |
|
| 2017 |
Tu HF, Zheng C, Xu RQ, Liu XJ, You SL. Iridium-Catalyzed Intermolecular Asymmetric Dearomatization of β-Naphthols with Allyl Alcohols or Allyl Ethers. Angewandte Chemie (International Ed. in English). PMID 28067451 DOI: 10.1002/Anie.201609654 |
0.68 |
|
| 2017 |
Wu W, Zhang L, You S. Recent Progress on Gold-catalyzed Dearomatization Reactions Acta Chimica Sinica. 75: 419. DOI: 10.6023/A17020049 |
0.657 |
|
| 2017 |
Wang J, Gao D, Huang J, Tang S, Xiong Z, Hu H, You S, Zhu Q. Palladium-Catalyzed Enantioselective C(sp2)–H Imidoylation by Desymmetrization Acs Catalysis. 7: 3832-3836. DOI: 10.1021/Acscatal.7B00731 |
0.843 |
|
| 2017 |
Wang S, Gu Q, You S. Cp*RhIII-Catalyzed C–H Amidation of Ferrocenes Organometallics. 36: 4359-4362. DOI: 10.1021/Acs.Organomet.7B00691 |
0.693 |
|
| 2017 |
You S. The 2016 Huang Yao-Zeng Organometallic Chemistry Award of the Chinese Chemical Society Organometallics. 36: 245-246. DOI: 10.1021/Acs.Organomet.6B00896 |
0.461 |
|
| 2017 |
Zhang X, You S. Removing the Mask in Catalytic Asymmetric Diamination of Alkenes Chem. 3: 919-921. DOI: 10.1016/J.Chempr.2017.11.012 |
0.679 |
|
| 2017 |
Cheng Q, Zhang H, Yue W, You S. Palladium-Catalyzed Highly Stereoselective Dearomative [3 + 2] Cycloaddition of Nitrobenzofurans Chem. 3: 428-436. DOI: 10.1016/J.Chempr.2017.06.015 |
0.696 |
|
| 2017 |
Lai Z, Liu C, Sun H, You S. Asymmetric Synthesis of 3-Allyloxindoles and 3-Allenyloxindoles by Scandium(III)-Catalyzed Claisen Rearrangement Reactions Chinese Journal of Chemistry. 35: 1512-1516. DOI: 10.1002/Cjoc.201700486 |
0.75 |
|
| 2017 |
Wang Y, Zheng C, You S. Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy Angewandte Chemie. 129: 15289-15293. DOI: 10.1002/ange.201708419 |
0.451 |
|
| 2017 |
Liu C, Yi J, Dai L, You S. Copper(I)-Catalyzed Cascade Dearomatization of Tryptophols with 3-Indolylphenyliodonium Salts Asian Journal of Organic Chemistry. 6: 1201-1204. DOI: 10.1002/Ajoc.201600626 |
0.71 |
|
| 2016 |
Wu QF, Zheng C, Zhuo CX, You SL. Highly efficient synthesis and stereoselective migration reactions of chiral five-membered aza-spiroindolenines: scope and mechanistic understanding. Chemical Science. 7: 4453-4459. PMID 30155093 DOI: 10.1039/C6Sc00176A |
0.748 |
|
| 2016 |
Wu WT, Xu RQ, Zhang L, You SL. Construction of spirocarbocycles gold-catalyzed intramolecular dearomatization of naphthols. Chemical Science. 7: 3427-3431. PMID 29997837 DOI: 10.1039/C5Sc04130A |
0.709 |
|
| 2016 |
Xu RQ, Yang P, Tu HF, Wang SG, You SL. Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of β-Naphthols. Angewandte Chemie (International Ed. in English). PMID 27791314 DOI: 10.1002/Anie.201608724 |
0.615 |
|
| 2016 |
Wang DC, Xie MS, Guo HM, Qu GR, Zhang MC, You SL. Enantioselective Dearomative [3+2] Cycloaddition Reactions of Benzothiazoles. Angewandte Chemie (International Ed. in English). PMID 27723190 DOI: 10.1002/Anie.201607852 |
0.736 |
|
| 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 |
0.683 |
|
| 2016 |
Liang XW, Zheng C, You SL. Dearomatization through Halofunctionalization Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27377184 DOI: 10.1002/Chem.201600885 |
0.673 |
|
| 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 |
0.717 |
|
| 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 |
0.701 |
|
| 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 |
0.725 |
|
| 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 |
0.694 |
|
| 2016 |
Zheng J, Cui WJ, Zheng C, You SL. Synthesis and Application of Chiral Spiro Cp Ligands in Rhodium-Catalyzed Asymmetric Oxidative Coupling of Biaryl Com-pounds with Alkenes. Journal of the American Chemical Society. PMID 27070297 DOI: 10.1021/Jacs.6B02302 |
0.67 |
|
| 2016 |
Gao DW, Gu Q, You SL. An Enantioselective Oxidative C-H/C-H Cross-Coupling Reaction: Highly Efficient Method To Prepare Planar Chiral Ferrocenes. Journal of the American Chemical Society. PMID 26891702 DOI: 10.1021/Jacs.6B00127 |
0.841 |
|
| 2016 |
Cheng Q, Wang Y, You SL. Chemo-, Diastereo-, and Enantioselective Iridium-Catalyzed Allylic Intramolecular Dearomatization Reaction of Naphthol Derivatives. Angewandte Chemie (International Ed. in English). PMID 26848021 DOI: 10.1002/Anie.201511519 |
0.721 |
|
| 2016 |
Wu WT, Zhang L, You SL. Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives. Chemical Society Reviews. PMID 26796922 DOI: 10.1039/C5Cs00356C |
0.685 |
|
| 2016 |
Zhou Y, Liu XW, Gu Q, You SL. Enantioselective Synthesis of Tetrahydroindolizines via Ruthenium-Chiral Phosphoric Acid Sequential Catalysis Synlett. 27: 586-590. DOI: 10.1055/S-0035-1560485 |
0.704 |
|
| 2016 |
Zhuo CX, Zhang X, You SL. Enantioselective Synthesis of Pyrrole-Fused Piperazine and Piperazinone Derivatives via Ir-Catalyzed Asymmetric Allylic Amination Acs Catalysis. 6: 5307-5310. DOI: 10.1021/Acscatal.6B01585 |
0.737 |
|
| 2016 |
Zheng C, Zheng J, You SL. A DFT Study on Rh-Catalyzed Asymmetric Dearomatization of 2-Naphthols Initiated with C-H Activation: A Refined Reaction Mechanism and Origins of Multiple Selectivity Acs Catalysis. 6: 262-271. DOI: 10.1021/Acscatal.5B01891 |
0.702 |
|
| 2016 |
Gao DW, Gu Y, Wang SB, Gu Q, You SL. Palladium(0)-catalyzed asymmetric C-H alkenylation for efficient synthesis of planar chiral ferrocenes Organometallics. 35: 3227-3233. DOI: 10.1021/Acs.Organomet.6B00569 |
0.854 |
|
| 2016 |
Zhang X, Liu W, Cheng Q, You S. Iridium-Catalyzed Asymmetric Allylic Amination Reactions with N-Aryl Phosphoramidite Ligands Organometallics. 35: 2467-2472. DOI: 10.1021/Acs.Organomet.6B00339 |
0.692 |
|
| 2016 |
Deng L, You S. Organometallics in Asia Organometallics. 35: 1341-1342. DOI: 10.1021/Acs.Organomet.6B00338 |
0.486 |
|
| 2016 |
Wang S, Zheng J, You S. Synthesis of Ferrocene-Based Pyridinones through Rh(III)-Catalyzed Direct C–H Functionalization Reaction Organometallics. 35: 1420-1425. DOI: 10.1021/Acs.Organomet.6B00020 |
0.715 |
|
| 2016 |
Zheng C, You S. Catalytic Asymmetric Dearomatization by Transition-Metal Catalysis: A Method for Transformations of Aromatic Compounds Chem. 1: 830-857. DOI: 10.1016/J.Chempr.2016.11.005 |
0.663 |
|
| 2016 |
Zhao Z, Gu Q, Wu X, You S. Enantioselective synthesis of 10-allylanthrones via iridium-catalyzed allylic substitution reaction Chinese Chemical Letters. 27: 619-622. DOI: 10.1016/J.Cclet.2016.02.017 |
0.761 |
|
| 2016 |
Wu W, Yang Z, You S. ChemInform Abstract: Asymmetric C-H Bond Insertion Reactions Cheminform. 47. DOI: 10.1002/chin.201647256 |
0.335 |
|
| 2016 |
Liang X, Zheng C, You S. ChemInform Abstract: Asymmetric [1,5]-Hydride Transfer Reactions Cheminform. 47. DOI: 10.1002/chin.201647255 |
0.377 |
|
| 2016 |
Kang Q, You S. ChemInform Abstract: Asymmetric Friedel-Crafts Alkylation Reactions Cheminform. 47. DOI: 10.1002/chin.201647254 |
0.488 |
|
| 2016 |
Wang S, You S. ChemInform Abstract: Asymmetric Cross-Dehydrogenative Coupling (CDC) Reactions Cheminform. 47. DOI: 10.1002/chin.201647245 |
0.37 |
|
| 2016 |
Liang X, Zheng C, You S. Catalytic Asymmetric Chlorinative Dearomatization Reaction of Benzofurans Advanced Synthesis & Catalysis. 358: 2066-2071. DOI: 10.1002/Adsc.201501184 |
0.731 |
|
| 2015 |
Li GT, Gu Q, You SL. Enantioselective annulation of enals with 2-naphthols by triazolium salts derived from l-phenylalanine. Chemical Science. 6: 4273-4278. PMID 29218195 DOI: 10.1039/C5Sc00731C |
0.708 |
|
| 2015 |
Yin Q, Wang SG, Liang XW, Gao DW, Zheng J, You SL. Organocatalytic asymmetric chlorinative dearomatization of naphthols. Chemical Science. 6: 4179-4183. PMID 29218183 DOI: 10.1039/C5Sc00494B |
0.86 |
|
| 2015 |
Zhang X, Liu WB, Tu HF, You SL. Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles. Chemical Science. 6: 4525-4529. PMID 29142701 DOI: 10.1039/C5Sc01772F |
0.731 |
|
| 2015 |
Yang ZP, Wu QF, Shao W, You SL. Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Pyridines, Pyrazines, Quinolines and Isoquinolines. Journal of the American Chemical Society. PMID 26605697 DOI: 10.1021/Jacs.5B10440 |
0.747 |
|
| 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 |
0.71 |
|
| 2015 |
Wang SG, Liu XJ, Zhao QC, Zheng C, Wang SB, You SL. Asymmetric Dearomatization of β-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction. Angewandte Chemie (International Ed. in English). PMID 26463712 DOI: 10.1002/Anie.201507998 |
0.696 |
|
| 2015 |
Zhuo CX, Zhou Y, Cheng Q, Huang L, You SL. Enantioselective Construction of Spiroindolines with Three Contiguous Stereogenic Centers and Chiral Tryptamine Derivatives via Reactive Spiroindolenine Intermediates. Angewandte Chemie (International Ed. in English). PMID 26403164 DOI: 10.1002/Anie.201507193 |
0.749 |
|
| 2015 |
Zhuo CX, Cheng Q, Liu WB, Zhao Q, You SL. Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions. Angewandte Chemie (International Ed. in English). PMID 26036866 DOI: 10.1002/Anie.201502259 |
0.723 |
|
| 2015 |
Shao W, Li H, Liu C, Liu CJ, You SL. Copper-Catalyzed Intermolecular Asymmetric Propargylic Dearomatization of Indoles. Angewandte Chemie (International Ed. in English). 54: 7684-7. PMID 25968474 DOI: 10.1002/Anie.201503042 |
0.728 |
|
| 2015 |
Zheng J, Wang SB, Zheng C, You SL. Asymmetric Dearomatization of Naphthols via a Rh-Catalyzed C(sp²)-H Functionalization/Annulation Reaction. Journal of the American Chemical Society. 137: 4880-3. PMID 25853771 DOI: 10.1021/Jacs.5B01707 |
0.703 |
|
| 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 |
0.711 |
|
| 2015 |
Zhao ZL, Xu QL, Gu Q, Wu XY, You SL. Enantioselective synthesis of 4-substituted tetrahydroisoquinolines via palladium-catalyzed intramolecular Friedel-Crafts type allylic alkylation of phenols. Organic & Biomolecular Chemistry. 13: 3086-92. PMID 25625805 DOI: 10.1039/C4Ob02574A |
0.724 |
|
| 2015 |
Zhang X, Yang ZP, Huang L, You SL. Highly regio- and enantioselective synthesis of N-substituted 2-pyridones: iridium-catalyzed intermolecular asymmetric allylic amination. Angewandte Chemie (International Ed. in English). 54: 1873-6. PMID 25504907 DOI: 10.1002/Anie.201409976 |
0.735 |
|
| 2015 |
Wang SG, Yin Q, Zhuo CX, You SL. Asymmetric dearomatization of β-naphthols through an amination reaction catalyzed by a chiral phosphoric acid. Angewandte Chemie (International Ed. in English). 54: 647-50. PMID 25414091 DOI: 10.1002/Anie.201409756 |
0.728 |
|
| 2015 |
Zhang X, Liu WB, Tu HF, You SL. Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles Chemical Science. 6: 4525-4529. DOI: 10.1039/c5sc01772f |
0.648 |
|
| 2015 |
Yin Q, Wang SG, Liang XW, Gao DW, Zheng J, You SL. Organocatalytic asymmetric chlorinative dearomatization of naphthols Chemical Science. 6: 4179-4183. DOI: 10.1039/c5sc00494b |
0.814 |
|
| 2015 |
Zhang JW, Liu XW, Gu Q, Shi XX, You SL. Enantioselective synthesis of 4,5,6,7-tetrahydroindoles via olefin cross-metathesis/intramolecular Friedel-Crafts alkylation reaction of pyrroles Organic Chemistry Frontiers. 2: 476-480. DOI: 10.1039/C5Qo00034C |
0.735 |
|
| 2015 |
Xu QL, You SL. CHAPTER 9: Asymmetric hydrovinylation reactions Rsc Catalysis Series. 2015: 384-404. DOI: 10.1039/9781782621966-00384 |
0.426 |
|
| 2015 |
Xu QL, You SL. CHAPTER 8: Asymmetric hydroacylation reactions Rsc Catalysis Series. 2015: 358-383. DOI: 10.1039/9781782621966-00358 |
0.429 |
|
| 2015 |
Kang Q, You SL. CHAPTER 6: Asymmetric friedel-crafts alkylation reactions Rsc Catalysis Series. 2015: 214-282. DOI: 10.1039/9781782621966-00214 |
0.476 |
|
| 2015 |
Gao DW, Zheng J, Ye KY, Zheng C, You SL. CHAPTER 5: Asymmetric functionalization of C-H bonds via a transient carbon-metal (C-M) species Rsc Catalysis Series. 2015: 141-213. DOI: 10.1039/9781782621966-00141 |
0.692 |
|
| 2015 |
Liang XW, Zheng C, You SL. CHAPTER 4: Asymmetric [1,5]-hydride transfer reactions Rsc Catalysis Series. 2015: 126-140. DOI: 10.1039/9781782621966-00126 |
0.358 |
|
| 2015 |
Zheng C, You SL. CHAPTER 3: Asymmetric oxidative biaryl coupling reactions Rsc Catalysis Series. 2015: 92-125. DOI: 10.1039/9781782621966-00092 |
0.332 |
|
| 2015 |
Wang SG, You SL. CHAPTER 2: Asymmetric cross-dehydrogenative coupling (CDC) reactions Rsc Catalysis Series. 2015: 67-91. DOI: 10.1039/9781782621966-00067 |
0.359 |
|
| 2015 |
Wu WT, Yang ZP, You SL. CHAPTER 1: Asymmetric C-H bond insertion reactions Rsc Catalysis Series. 2015: 1-66. DOI: 10.1039/9781782621966-00001 |
0.322 |
|
| 2015 |
Gao DW, Zheng C, Gu Q, You SL. Pd-Catalyzed Highly Enantioselective Synthesis of Planar Chiral Ferrocenylpyridine Derivatives Organometallics. 34: 4618-4625. DOI: 10.1021/Acs.Organomet.5B00730 |
0.844 |
|
| 2015 |
Zhao ZL, Gu Q, Wu XY, You SL. Pd(0)-catalyzed benzylation of indole through η3-benzyl palladium intermediate Cuihua Xuebao/Chinese Journal of Catalysis. 36: 15-18. DOI: 10.1016/S1872-2067(14)60191-1 |
0.62 |
|
| 2015 |
You S, Latendresse CA, Fernandes SC, Sullivan KM, Euler WB. Detection of dinitrotoluene isomers using reactions with bases: A structural, spectroscopic, kinetic, and computational study Sensors and Actuators, B: Chemical. 216: 165-175. DOI: 10.1016/J.Snb.2015.04.033 |
0.338 |
|
| 2015 |
Kim B, You S, Lee N, Choi S. Efficient synthesis of unsymmetrical 1,3-diynes utilizing a palladium-catalyzed cross-coupling reaction without homo-coupling Bulletin of the Korean Chemical Society. 36: 360-362. DOI: 10.1002/bkcs.10004 |
0.576 |
|
| 2015 |
Han L, Zhang W, Shi XX, You SL. Dearomatization of Indoles via a Phenol-Directed Vanadium- Catalyzed Asymmetric Epoxidation and Ring-Opening Cascade Advanced Synthesis and Catalysis. 357: 3064-3068. DOI: 10.1002/Adsc.201500557 |
0.68 |
|
| 2015 |
Zhou Y, Zhuo CX, Gu Q, You SL. Intermolecular dearomatization reaction of pyrroles promoted by silica gel Advanced Synthesis and Catalysis. 357: 912-916. DOI: 10.1002/Adsc.201401150 |
0.68 |
|
| 2014 |
Zheng J, You SL. Construction of axial chirality by rhodium-catalyzed asymmetric dehydrogenative Heck coupling of biaryl compounds with alkenes. Angewandte Chemie (International Ed. in English). 53: 13244-7. PMID 25346171 DOI: 10.1002/Anie.201408805 |
0.709 |
|
| 2014 |
Zheng C, Zhuo CX, You SL. Mechanistic insights into the Pd-catalyzed intermolecular asymmetric allylic dearomatization of multisubstituted pyrroles: understanding the remarkable regio- and enantioselectivity. Journal of the American Chemical Society. 136: 16251-9. PMID 25339156 DOI: 10.1021/Ja5080135 |
0.694 |
|
| 2014 |
Xu RQ, Gu Q, Wu WT, Zhao ZA, You SL. Construction of erythrinane skeleton via Pd(0)-catalyzed intramolecular dearomatization of para-aminophenols. Journal of the American Chemical Society. 136: 15469-72. PMID 25308898 DOI: 10.1021/Ja508645J |
0.62 |
|
| 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 |
0.726 |
|
| 2014 |
Yang ZP, Zhang W, You SL. Catalytic asymmetric reactions by metal and chiral phosphoric acid sequential catalysis. The Journal of Organic Chemistry. 79: 7785-98. PMID 25116832 DOI: 10.1021/Jo501300K |
0.667 |
|
| 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 |
0.666 |
|
| 2014 |
Lai ZW, Yang RF, Ye KY, Sun H, You SL. Synthesis of 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates. Beilstein Journal of Organic Chemistry. 10: 1261-6. PMID 24991277 DOI: 10.3762/Bjoc.10.126 |
0.655 |
|
| 2014 |
Zhuo CX, Zheng C, You SL. Transition-metal-catalyzed asymmetric allylic dearomatization reactions. Accounts of Chemical Research. 47: 2558-73. PMID 24940612 DOI: 10.1021/Ar500167F |
0.717 |
|
| 2014 |
Zheng J, You SL. Rhodium-catalyzed direct coupling of biaryl pyridine derivatives with internal alkynes. Chemical Communications (Cambridge, England). 50: 8204-7. PMID 24931462 DOI: 10.1039/C4Cc02822H |
0.697 |
|
| 2014 |
Yang ZP, Wu QF, You SL. Direct asymmetric dearomatization of pyridines and pyrazines by iridium-catalyzed allylic amination reactions. Angewandte Chemie (International Ed. in English). 53: 6986-9. PMID 24861469 DOI: 10.1002/Anie.201404286 |
0.752 |
|
| 2014 |
Zhuo CX, Zhou Y, You SL. Highly regio- and enantioselective synthesis of polysubstituted 2H-pyrroles via Pd-catalyzed intermolecular asymmetric allylic dearomatization of pyrroles. Journal of the American Chemical Society. 136: 6590-3. PMID 24758260 DOI: 10.1021/Ja5028138 |
0.701 |
|
| 2014 |
Yin Q, You SL. Asymmetric chlorocyclization of indole-3-yl-benzamides for the construction of fused indolines. Organic Letters. 16: 2426-9. PMID 24730758 DOI: 10.1021/Ol5007532 |
0.652 |
|
| 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 |
0.668 |
|
| 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 |
0.727 |
|
| 2014 |
Gao DW, Yin Q, Gu Q, You SL. Enantioselective synthesis of planar chiral ferrocenes via Pd(0)-catalyzed intramolecular direct C-H bond arylation. Journal of the American Chemical Society. 136: 4841-4. PMID 24625115 DOI: 10.1021/Ja500444V |
0.854 |
|
| 2014 |
Yin Q, You SL. Asymmetric chlorination/ring expansion for the synthesis of α-quaternary cycloalkanones. Organic Letters. 16: 1810-3. PMID 24617607 DOI: 10.1021/Ol5005565 |
0.668 |
|
| 2014 |
Li W, Liu C, Zhang H, Ye K, Zhang G, Zhang W, Duan Z, You S, Lei A. Palladium-catalyzed oxidative carbonylation of N-allylamines for the synthesis of β-lactams Angewandte Chemie - International Edition. 53: 2443-2446. PMID 24474421 DOI: 10.1002/Anie.201309081 |
0.63 |
|
| 2014 |
Wang SG, You SL. Hydrogenative dearomatization of pyridine and an asymmetric aza-Friedel-Crafts alkylation sequence. Angewandte Chemie (International Ed. in English). 53: 2194-7. PMID 24470000 DOI: 10.1002/Anie.201309876 |
0.728 |
|
| 2014 |
Liu H, Zheng C, You SL. Catalytic C6 functionalization of 2,3-disubstituted indoles by scandium triflate. The Journal of Organic Chemistry. 79: 1047-54. PMID 24410592 DOI: 10.1021/Jo402511B |
0.633 |
|
| 2014 |
Han L, Liu C, Zhang W, Shi XX, You SL. Dearomatization of tryptophols via a vanadium-catalyzed asymmetric epoxidation and ring-opening cascade. Chemical Communications (Cambridge, England). 50: 1231-3. PMID 24336475 DOI: 10.1039/C3Cc47921H |
0.742 |
|
| 2014 |
Duan D, Yin Q, Wang S, Gu Q, You S. Chiral phosphoric acid-catalyzed asymmetric cascade reaction of C(3) substituted indoles and methyl vinyl ketone Acta Chimica Sinica. 72: 1001-1004. DOI: 10.6023/A14060497 |
0.506 |
|
| 2014 |
Zhao Q, Zhuo CX, You SL. Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines Rsc Advances. 4: 10875-10878. DOI: 10.1039/C4Ra00701H |
0.695 |
|
| 2014 |
Zhang X, Han L, You SL. Ir-catalyzed intermolecular asymmetric allylic dearomatization reaction of indoles Chemical Science. 5: 1059-1063. DOI: 10.1039/C3Sc53019A |
0.727 |
|
| 2014 |
Zheng C, You SL. Recent development of direct asymmetric functionalization of inert C-H bonds Rsc Advances. 4: 6173-6214. DOI: 10.1039/C3Ra46996D |
0.533 |
|
| 2014 |
Shi YC, Wang SG, Yin Q, You SL. N-alkylation of indole via ring-closing metathesis/isomerization/Mannich cascade under ruthenium/chiral phosphoric acid sequential catalysis Organic Chemistry Frontiers. 1: 39-43. DOI: 10.1039/C3Qo00008G |
0.706 |
|
| 2014 |
Gao DW, Gu Q, You SL. Pd(II)-catalyzed intermolecular direct C-H bond iodination: An efficient approach toward the synthesis of axially chiral compounds via kinetic resolution Acs Catalysis. 4: 2741-2745. DOI: 10.1021/Cs500813Z |
0.834 |
|
| 2014 |
Liu H, Zheng C, You SL. Fe(OTf)3 Catalyzed annulation of 2,3-disubstituted indoles with aziridines Chinese Journal of Chemistry. DOI: 10.1002/Cjoc.201400178 |
0.66 |
|
| 2014 |
Cai Q, Yin Q, You SL. Chiral-amine-catalyzed asymmetric bromocyclization of tryptamine derivatives Asian Journal of Organic Chemistry. 3: 408-411. DOI: 10.1002/Ajoc.201300146 |
0.706 |
|
| 2014 |
Zhuo CX, You SL. Palladium-catalyzed intermolecular allylic dearomatization reaction of α-substituted β-naphthol derivatives: Scope and mechanistic investigation Advanced Synthesis and Catalysis. 356: 2020-2028. DOI: 10.1002/Adsc.201400154 |
0.658 |
|
| 2014 |
Yang ZP, Zhuo CX, You SL. Ruthenium-catalyzed intramolecular allylic dearomatization/migration reaction of indoles and pyrroles Advanced Synthesis and Catalysis. 356: 1731-1734. DOI: 10.1002/Adsc.201301083 |
0.722 |
|
| 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 |
0.757 |
|
| 2013 |
Shi YC, Yang RF, Gao DW, You SL. Enantioselective synthesis of planar chiral ferrocenes via palladium-catalyzed annulation with diarylethynes. Beilstein Journal of Organic Chemistry. 9: 1891-6. PMID 24062858 DOI: 10.3762/Bjoc.9.222 |
0.839 |
|
| 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 |
0.739 |
|
| 2013 |
Zhuo CX, You SL. Palladium-catalyzed intermolecular asymmetric allylic dearomatization reaction of naphthol derivatives. Angewandte Chemie (International Ed. in English). 52: 10056-9. PMID 23934955 DOI: 10.1002/Anie.201304591 |
0.741 |
|
| 2013 |
Yin Q, You SL. Enantioselective chlorocyclization of indole derived benzamides for the synthesis of spiro-indolines. Organic Letters. 15: 4266-9. PMID 23909796 DOI: 10.1021/Ol4020943 |
0.674 |
|
| 2013 |
Zhang JW, Cai Q, Gu Q, Shi XX, You SL. Enantioselective synthesis of benzofurans and benzoxazines via an olefin cross-metathesis-intramolecular oxo-Michael reaction. Chemical Communications (Cambridge, England). 49: 7750-2. PMID 23884172 DOI: 10.1039/C3Cc43937B |
0.746 |
|
| 2013 |
Zhang X, Liu WB, Wu QF, You SL. Ruthenium-catalyzed intramolecular allylic dearomatization reaction of indole derivatives. Organic Letters. 15: 3746-9. PMID 23841581 DOI: 10.1021/Ol4016578 |
0.732 |
|
| 2013 |
Zhuo CX, Wu QF, Zhao Q, Xu QL, You SL. Enantioselective functionalization of indoles and pyrroles via an in situ-formed spiro intermediate. Journal of the American Chemical Society. 135: 8169-72. PMID 23672506 DOI: 10.1021/Ja403535A |
0.681 |
|
| 2013 |
Yin Q, Wang SG, You SL. Asymmetric synthesis of tetrahydro-β-carbolines via chiral phosphoric acid catalyzed transfer hydrogenation reaction. Organic Letters. 15: 2688-91. PMID 23668420 DOI: 10.1021/Ol400995C |
0.678 |
|
| 2013 |
Zheng C, Wu QF, You SL. A combined theoretical and experimental investigation into the highly stereoselective migration of spiroindolenines. The Journal of Organic Chemistry. 78: 4357-65. PMID 23578142 DOI: 10.1021/Jo400365E |
0.582 |
|
| 2013 |
Wang SG, Zhang W, You SL. Construction of spiro-tetrahydroquinolines via intramolecular dearomatization of quinolines: free of a preinstalled activation group. Organic Letters. 15: 1488-91. PMID 23470202 DOI: 10.1021/Ol4002416 |
0.702 |
|
| 2013 |
Cai Q, Liang XW, Wang SG, You SL. An olefin isomerization/asymmetric Pictet-Spengler cascade via sequential catalysis of ruthenium alkylidene and chiral phosphoric acid. Organic & Biomolecular Chemistry. 11: 1602-5. PMID 23364474 DOI: 10.1039/C3Ob00072A |
0.713 |
|
| 2013 |
Gao DW, Shi YC, Gu Q, Zhao ZL, You SL. Enantioselective synthesis of planar chiral ferrocenes via palladium-catalyzed direct coupling with arylboronic acids. Journal of the American Chemical Society. 135: 86-9. PMID 23253097 DOI: 10.1021/Ja311082U |
0.84 |
|
| 2013 |
Ye KY, Zhao ZA, Lai ZW, Dai LX, You SL. Highly regioselective allylic substitution reactions catalyzed by an air-stable (π-Allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand Synthesis (Germany). 45: 2109-2114. DOI: 10.1055/S-0033-1339187 |
0.71 |
|
| 2013 |
Jia MQ, You SL. Desymmetrization of cyclohexadienones via intramolecular stetter reaction to construct tricyclic carbocycles Synlett. 24: 1201-1204. DOI: 10.1055/S-0033-1338838 |
0.69 |
|
| 2013 |
Zhang X, Yang ZP, Liu C, You SL. Ru-catalyzed intermolecular dearomatization reaction of indoles with allylic alcohols Chemical Science. 4: 3239-3243. DOI: 10.1039/C3Sc51313K |
0.684 |
|
| 2013 |
Xu QL, Dai LX, You SL. Diversity oriented synthesis of indole-based peri-annulated compounds via allylic alkylation reactions Chemical Science. 4: 97-102. DOI: 10.1039/C2Sc21085A |
0.714 |
|
| 2013 |
Jia MQ, You SL. N-heterocyclic carbene-catalyzed enantioselective intramolecular N-tethered aldehyde-ketone benzoin reactions Acs Catalysis. 3: 622-624. DOI: 10.1021/Cs4000014 |
0.688 |
|
| 2013 |
Ye KY, Dai LX, You SL. Synthesis of 1Z,4E,6E-Triene Derivatives by Chemo- and Regioselective Iridium-Catalyzed Dienylation of ortho-Aminostyrenes with Dienyl Carbonates Asian Journal of Organic Chemistry. 2: 244-249. DOI: 10.1002/Ajoc.201300015 |
0.618 |
|
| 2012 |
Zhuo CX, Zhang W, You SL. Catalytic asymmetric dearomatization reactions. Angewandte Chemie (International Ed. in English). 51: 12662-86. PMID 23208999 DOI: 10.1002/Anie.201204822 |
0.698 |
|
| 2012 |
Jia MQ, Liu C, You SL. Diastereoselective and enantioselective desymmetrization of α-substituted cyclohexadienones via intramolecular Stetter reaction. The Journal of Organic Chemistry. 77: 10996-1001. PMID 23140505 DOI: 10.1021/Jo3022555 |
0.741 |
|
| 2012 |
Cai Q, Liang XW, Wang SG, Zhang JW, Zhang X, You SL. Ring-closing metathesis/isomerization/Pictet-Spengler cascade via ruthenium/chiral phosphoric acid sequential catalysis. Organic Letters. 14: 5022-5. PMID 22988945 DOI: 10.1021/Ol302215U |
0.715 |
|
| 2012 |
Cai Q, Liu C, Liang XW, You SL. Enantioselective construction of pyrroloindolines via chiral phosphoric acid catalyzed cascade Michael addition-cyclization of tryptamines. Organic Letters. 14: 4588-90. PMID 22928846 DOI: 10.1021/Ol302043S |
0.69 |
|
| 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 |
0.702 |
|
| 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 |
0.714 |
|
| 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 |
0.719 |
|
| 2012 |
Yin Q, You SL. Intramolecular alkene electrophilic bromination initiated ipso-bromocyclization for the synthesis of functionalized azaspirocyclohexadienones. Organic Letters. 14: 3526-9. PMID 22724508 DOI: 10.1021/Ol301531Z |
0.671 |
|
| 2012 |
Cai Q, You SL. Organocatalyzed enantioselective formal [4 + 2] cycloaddition of 2,3-disubstituted indole and methyl vinyl ketone. Organic Letters. 14: 3040-3. PMID 22626008 DOI: 10.1021/Ol301114Z |
0.681 |
|
| 2012 |
Jia MQ, You SL. Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction. Chemical Communications (Cambridge, England). PMID 22618513 DOI: 10.1039/C2Cc32783J |
0.729 |
|
| 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 |
0.748 |
|
| 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 |
0.691 |
|
| 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 |
0.737 |
|
| 2012 |
Wang SG, Han L, Zeng M, Sun FL, Zhang W, You SL. Enantioselective synthesis of fluorene derivatives by chiral N-triflyl phosphoramide catalyzed double Friedel-Crafts alkylation reaction. Organic & Biomolecular Chemistry. 10: 3202-9. PMID 22411157 DOI: 10.1039/C2Ob07168A |
0.741 |
|
| 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 |
0.698 |
|
| 2012 |
Zheng C, You SL. Transfer hydrogenation with Hantzsch esters and related organic hydride donors. Chemical Society Reviews. 41: 2498-518. PMID 22282764 DOI: 10.1039/C1Cs15268H |
0.622 |
|
| 2012 |
Wu QF, Zheng C, You SL. Enantioselective synthesis of spiro cyclopentane-1,3'-indoles and 2,3,4,9-tetrahydro-1H-carbazoles by iridium-catalyzed allylic dearomatization and stereospecific migration. Angewandte Chemie (International Ed. in English). 51: 1680-3. PMID 22223488 DOI: 10.1002/Anie.201107677 |
0.669 |
|
| 2012 |
Zhuo C, Liu W, Wu Q, You S. Asymmetric dearomatization of pyrrolesviaIr-catalyzed allylic substitution reaction: enantioselective synthesis of spiro-2H-pyrroles Chem. Sci.. 3: 205-208. DOI: 10.1039/C1Sc00517K |
0.748 |
|
| 2012 |
Zhang JW, Xu Z, Gu Q, Shi XX, Leng XB, You SL. Chiral counteranion-directed silver-catalyzed asymmetric synthesis of 1,2-dihydroisoquinolines by Friedel-Crafts alkylation reactions Tetrahedron. 68: 5263-5268. DOI: 10.1016/J.Tet.2012.02.058 |
0.732 |
|
| 2012 |
You S. Special issue of "asymmetric synthesis" Chinese Journal of Chemistry. 30: 2603. DOI: 10.1002/Cjoc.201290030 |
0.611 |
|
| 2012 |
Zeng M, Zhang W, You S. One-pot synthesis of pyrrolo[1,2-a]indoles by chiral N-triflyl phosphoramide catalyzed Friedel-Crafts alkylation of 4,7-dihydroindole with β,γ-unsaturated α-keto esters Chinese Journal of Chemistry. 30: 2615-2623. DOI: 10.1002/Cjoc.201200759 |
0.701 |
|
| 2012 |
Zhuo C, Zhang W, You S. Katalytische asymmetrische Desaromatisierungen Angewandte Chemie. 124: 12834-12858. DOI: 10.1002/Ange.201204822 |
0.569 |
|
| 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 |
0.647 |
|
| 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 |
0.731 |
|
| 2012 |
Engle KM, Yu JQ, Davies HML, Xi Z, You SL, Shi ZJ. Transition Metal-Catalyzed C-H Functionalization: Synthetically Enabling Reactions for Building Molecular Complexity Organic Chemistry - Breakthroughs and Perspectives. 279-333. DOI: 10.1002/9783527664801.ch8 |
0.617 |
|
| 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 |
0.735 |
|
| 2011 |
Gu Q, You SL. Desymmetrization of cyclohexadienones via asymmetric Michael reaction catalyzed by cinchonine-derived urea. Organic Letters. 13: 5192-5. PMID 21913734 DOI: 10.1021/Ol202073P |
0.739 |
|
| 2011 |
Cai Q, Zheng C, Zhang JW, You SL. Enantioselective Michael/Mannich polycyclization cascade of indolyl enones catalyzed by quinine-derived primary amines. Angewandte Chemie (International Ed. in English). 50: 8665-9. PMID 21793147 DOI: 10.1002/Anie.201103937 |
0.691 |
|
| 2011 |
Rong ZQ, Jia MQ, You SL. Enantioselective N-heterocyclic carbene-catalyzed Michael addition to α,β-unsaturated aldehydes by redox oxidation. Organic Letters. 13: 4080-3. PMID 21732659 DOI: 10.1021/Ol201595F |
0.617 |
|
| 2011 |
Su H, Xie Y, Liu WB, You SL. Methyl-monofluorination of ibuprofen selectively increases its inhibitory activity toward cyclooxygenase-1 leading to enhanced analgesic activity and reduced gastric damage in vivo. Bioorganic & Medicinal Chemistry Letters. 21: 3578-82. PMID 21602044 DOI: 10.1016/J.Bmcl.2011.04.114 |
0.505 |
|
| 2011 |
Wu QF, Liu WB, Zhuo CX, Rong ZQ, Ye KY, You SL. Iridium-catalyzed intramolecular asymmetric allylic dearomatization of phenols. Angewandte Chemie (International Ed. in English). 50: 4455-8. PMID 21472834 DOI: 10.1002/Anie.201100206 |
0.744 |
|
| 2011 |
Jia MQ, Li Y, Rong ZQ, You SL. Synthesis of (1R,2R)-DPEN-derived triazolium salts and their application in asymmetric intramolecular Stetter reactions. Organic & Biomolecular Chemistry. 9: 2072-4. PMID 21340086 DOI: 10.1039/C1Ob00025J |
0.667 |
|
| 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 |
0.698 |
|
| 2011 |
Rong Z, Zhang W, Yang G, You S. N-Heterocyclic Carbene-Catalyzed Redox Reactions of α-Functionalized Aldehydes Current Organic Chemistry. 15: 3077-3090. DOI: 10.2174/138527211798357182 |
0.654 |
|
| 2011 |
Zhang J, Cai Q, Shi X, Zhang W, You S. Enantioselective Synthesisof Tetrahydropyrano[3,4-b]indolesCatalyzed by Chiral N-Triflyl Phosphoramidevia Intramolecular Friedel-Crafts Alkylation Reaction Synlett. 2011: 1239-1242. DOI: 10.1055/S-0030-1260537 |
0.719 |
|
| 2011 |
Rong Z, Li Y, Yang G, You S. d-Camphor-DerivedTriazolium Salts for Enantioselective Intramolecular Stetter Reactions Synlett. 2011: 1033-1037. DOI: 10.1055/S-0030-1259732 |
0.71 |
|
| 2011 |
Yin Q, You SL. Chiral phosphoric acid-catalysed Friedel-Crafts alkylation reaction of indoles with racemic spiro indolin-3-ones Chemical Science. 2: 1344-1348. DOI: 10.1039/C1Sc00190F |
0.725 |
|
| 2011 |
Gu Q, You S. Desymmetrization of cyclohexadienones via cinchonine derived thiourea-catalyzed enantioselective aza-Michael reaction and total synthesis of (-)-Mesembrine Chemical Science. 2: 1519. DOI: 10.1039/C1Sc00083G |
0.759 |
|
| 2011 |
Rong Z, Jia M, You S. (1R,2R)-DPEN-derived triazolium salts for enantioselective oxodiene Diels–Alder reactions Tetrahedron. 67: 9329-9333. DOI: 10.1016/J.Tet.2011.09.129 |
0.609 |
|
| 2011 |
Rong Z, Li Y, Yang G, You S. ChemInform Abstract: D-Camphor-Derived Triazolium Salts for Enantioselective Intramolecular Stetter Reactions. Cheminform. 42: no-no. DOI: 10.1002/chin.201135148 |
0.421 |
|
| 2010 |
You SL, Xia JB. Palladium-catalyzed aryl-aryl bond formation through double C-H activation. Topics in Current Chemistry. 292: 165-94. PMID 21500406 DOI: 10.1007/128_2009_18 |
0.672 |
|
| 2010 |
Cai Q, Zheng C, You SL. Enantioselective intramolecular aza-Michael additions of indoles catalyzed by chiral phosphoric acids. Angewandte Chemie (International Ed. in English). 49: 8666-9. PMID 20931585 DOI: 10.1002/Anie.201003919 |
0.684 |
|
| 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 |
0.744 |
|
| 2010 |
Wu QF, He H, Liu WB, You SL. Enantioselective construction of spiroindolenines by Ir-catalyzed allylic alkylation reactions. Journal of the American Chemical Society. 132: 11418-9. PMID 20677752 DOI: 10.1021/Ja105111N |
0.679 |
|
| 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 |
0.675 |
|
| 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 |
0.738 |
|
| 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 |
0.712 |
|
| 2010 |
Xia JB, Liu WB, Wang TM, You SL. Enantioselective synthesis of 3-azabicyclo[4.1.0]heptenes and 3-azabicyclo[3.2.0]heptenes by Ir-catalyzed asymmetric allylic amination of N-tosyl propynylamine and Pt-catalyzed cycloisomerization. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 6442-6. PMID 20449858 DOI: 10.1002/Chem.201000467 |
0.675 |
|
| 2010 |
Gu Q, Rong ZQ, Zheng C, You SL. Desymmetrization of cyclohexadienones via Brønsted acid-catalyzed enantioselective oxo-Michael reaction. Journal of the American Chemical Society. 132: 4056-7. PMID 20205477 DOI: 10.1021/Ja100207S |
0.735 |
|
| 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 |
0.7 |
|
| 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 |
0.705 |
|
| 2010 |
You S, Feng Z, Xu Q, Dai L. Enantioselective synthesis of 2-aryl-2,3-dihydro-4-quinolones by chiral Bronsted acid catalyzed intramolecular aza-Michael addition reaction Heterocycles. 80: 765-771. DOI: 10.3987/Com-09-S(S)66 |
0.741 |
|
| 2010 |
You S, Cai Q, Zheng C. Intramolecular Aza-Michael Addition of Indoles Synfacts. 2010: 1428-1428. DOI: 10.1055/S-0030-1258922 |
0.475 |
|
| 2010 |
Zheng C, Sheng Y, Li Y, You S. A theoretical investigation into chiral phosphoric acid-catalyzed asymmetric Friedel–Crafts reactions of nitroolefins and 4,7-dihydroindoles: reactivity and enantioselectivity Tetrahedron. 66: 2875-2880. DOI: 10.1016/J.Tet.2010.02.031 |
0.703 |
|
| 2010 |
Feng Z, Zeng M, Xu Q, You S. Asymmetric intramolecular oxa-Michael addition of activated α,β-unsaturated ketones by chiral N-triflyl phosphoramide Chinese Science Bulletin. 55: 1723-1725. DOI: 10.1007/S11434-009-3735-X |
0.61 |
|
| 2010 |
Xia J, Zhuo C, You S. Synthesis of cyclopropane-containing building blocks via Ir-catalyzed enantioselective allylic substitution reaction Chinese Journal of Chemistry. 28: 1525-1528. DOI: 10.1002/Cjoc.201090259 |
0.728 |
|
| 2010 |
Peng H, Dai L, You S. Enantioselektive palladiumkatalysierte direkte Alkylierung und Olefinierung von einfachen Arenen Angewandte Chemie. 122: 5962-5964. DOI: 10.1002/Ange.201000799 |
0.434 |
|
| 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 |
0.641 |
|
| 2009 |
Li Y, Wang XQ, Zheng C, You SL. Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts. Chemical Communications (Cambridge, England). 5823-5. PMID 19787109 DOI: 10.1039/B914805A |
0.741 |
|
| 2009 |
Cai Q, Zhao ZA, You SL. Asymmetric construction of polycyclic indoles through olefin cross-metathesis/intramolecular Friedel-Crafts alkylation under sequential catalysis. Angewandte Chemie (International Ed. in English). 48: 7428-31. PMID 19739165 DOI: 10.1002/Anie.200903462 |
0.651 |
|
| 2009 |
Sun FL, Zeng M, Gu Q, You SL. Enantioselective synthesis of fluorene derivatives by chiral phosphoric acid catalyzed tandem double Friedel-Crafts reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 8709-12. PMID 19644985 DOI: 10.1002/Chem.200901369 |
0.741 |
|
| 2009 |
Sheng YF, Gu Q, Zhang AJ, You SL. Chiral Brønsted acid-catalyzed asymmetric Friedel-Crafts alkylation of pyrroles with nitroolefins. The Journal of Organic Chemistry. 74: 6899-901. PMID 19639942 DOI: 10.1021/Jo9013029 |
0.737 |
|
| 2009 |
You SL, Cai Q, Zeng M. Chiral Brønsted acid catalyzed Friedel-Crafts alkylation reactions. Chemical Society Reviews. 38: 2190-201. PMID 19623343 DOI: 10.1039/B817310A |
0.704 |
|
| 2009 |
Li Y, Shi FQ, He QL, You SL. N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with arylsulfonyl indoles. Organic Letters. 11: 3182-5. PMID 19580259 DOI: 10.1021/Ol9013238 |
0.727 |
|
| 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 |
0.716 |
|
| 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 |
0.617 |
|
| 2009 |
Xia JB, You SL. Synthesis of 3-haloindolizines by copper(II) halide mediated direct functionalization of indolizines. Organic Letters. 11: 1187-90. PMID 19243196 DOI: 10.1021/ol9000872 |
0.585 |
|
| 2009 |
Sheng YF, Li GQ, Kang Q, Zhang AJ, You SL. Asymmetric Friedel-Crafts reaction of 4,7-dihydroindoles with nitroolefins by chiral Brønsted acids under low catalyst loading. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 3351-4. PMID 19229929 DOI: 10.1002/Chem.200900033 |
0.707 |
|
| 2009 |
Xia JB, Wang XQ, You SL. Synthesis of biindolizines through highly regioselective palladium-catalyzed C-H functionalization. The Journal of Organic Chemistry. 74: 456-8. PMID 19053600 DOI: 10.1021/Jo802227U |
0.682 |
|
| 2009 |
You S, Cai Q, Zhao Z. Asymmetric Construction of Polycyclic Indoles via Sequential Catalysis Synfacts. 2009: 1375-1375. DOI: 10.1055/S-0029-1218243 |
0.332 |
|
| 2009 |
You S, Liu W, He H, Dai L. Synthesis of 2-Methylindoline- and 2-Methyl-1,2,3,4-tetrahydroquinoline-Derived Phosphoramidites and Their Applications in Iridium-Catalyzed Allylic Alkylation of Indoles Synthesis. 2009: 2076-2082. DOI: 10.1055/S-0029-1216823 |
0.669 |
|
| 2009 |
He Q, Sun F, Zheng X, You S. Brønsted Acid CatalyzedSynthesis of Unsymmetrical Arylbis(3-indolyl)-methanes Synlett. 2009: 1111-1114. DOI: 10.1055/S-0028-1088109 |
0.695 |
|
| 2009 |
Kang Q, Zhao Z, You S. Enantioselective synthesis of (3-indolyl)glycine derivatives via asymmetric Friedel–Crafts reaction between indoles and glyoxylate imines Tetrahedron. 65: 1603-1607. DOI: 10.1016/J.Tet.2008.12.061 |
0.756 |
|
| 2009 |
Wang X, Xia J, Dai X, You S. Preparation of ferrocenyl imidazolines using bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate Science in China Series B: Chemistry. 52: 1331-1336. DOI: 10.1007/S11426-009-0161-5 |
0.627 |
|
| 2009 |
Sun F, Zheng X, Gu Q, He Q, You S. Enantioselective Synthesis of Unsymmetrical Triarylmethanes by Chiral Brønsted Acids European Journal of Organic Chemistry. 2010: 47-50. DOI: 10.1002/Ejoc.200901164 |
0.675 |
|
| 2008 |
Li Y, Feng Z, You SL. D-Camphor-derived triazolium salts for catalytic intramolecular crossed aldehyde-ketone benzoin reactions. Chemical Communications (Cambridge, England). 2263-5. PMID 18463760 DOI: 10.1039/B801004H |
0.687 |
|
| 2008 |
Kang Q, Zhao ZA, You SL. Asymmetric transfer hydrogenation of beta,gamma-alkynyl alpha-imino esters by a Brønsted acid. Organic Letters. 10: 2031-4. PMID 18422288 DOI: 10.1021/Ol800494R |
0.544 |
|
| 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 |
0.65 |
|
| 2008 |
Kang Q, Zheng XJ, You SL. Highly enantioselective friedel-crafts reaction of 4,7-dihydroindoles with imines by chiral phosphoric acids: facile access to 2-indolyl methanamine derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 3539-42. PMID 18327877 DOI: 10.1002/Chem.200800263 |
0.722 |
|
| 2008 |
You S, Liu W, He H, Dai L. Iridium-Catalyzed Friedel-Crafts-Type Allylic Alkylation of Indoles Synfacts. 2008: 0717-0717. DOI: 10.1055/s-2008-1077842 |
0.409 |
|
| 2008 |
Zeng M, Kang Q, He Q, You S. Highly Enantioselective Friedel-Crafts Reaction of 4,7-Dihydroindoles with β,γ-Unsaturated α-Keto Esters by Chiral Brønsted Acids Advanced Synthesis & Catalysis. 350: 2169-2173. DOI: 10.1002/Adsc.200800523 |
0.675 |
|
| 2008 |
Li Y, Zhao Z, He H, You S. Stereoselective Synthesis of γ-ButyrolactonesviaOrganocatalytic Annulations of Enals and Keto Esters Advanced Synthesis & Catalysis. 350: 1885-1890. DOI: 10.1002/Adsc.200800251 |
0.67 |
|
| 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 |
0.7 |
|
| 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 |
0.656 |
|
| 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 |
0.653 |
|
| 2007 |
You SL. Recent developments in asymmetric transfer hydrogenation with Hantzsch esters: a biomimetic approach. Chemistry, An Asian Journal. 2: 820-7. PMID 17551915 DOI: 10.1002/Asia.200700081 |
0.591 |
|
| 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 |
0.629 |
|
| 2007 |
Kang Q, Zhao ZA, You SL. Highly enantioselective Friedel-Crafts reaction of indoles with imines by a chiral phosphoric acid. Journal of the American Chemical Society. 129: 1484-5. PMID 17283980 DOI: 10.1021/Ja067417A |
0.731 |
|
| 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 |
0.755 |
|
| 2007 |
You S, Kang Q, Zhao Z. Asymmetric Synthesis of 3-Indolyl Methylamines (Gramines) Synfacts. 2007: 0471-0471. DOI: 10.1055/s-2007-968473 |
0.403 |
|
| 2007 |
You S, Kang Q, Zhao Z. Phosphoric Acid Catalyzed Friedel-Crafts Reaction of Indoles with Imines Synfacts. 2007: 0547-0547. DOI: 10.1055/s-2007-968349 |
0.447 |
|
| 2007 |
Xia J, You S. Carbon−Carbon Bond Formation through Double sp2C−H Activations: Synthesis of Ferrocenyl Oxazoline Derivatives Organometallics. 26: 4869-4871. DOI: 10.1021/Om700806E |
0.656 |
|
| 2007 |
Kang Q, Zhao Z, You S. Highly Enantioselective Transfer Hydrogenation of α-Imino Esters by a Phosphoric Acid Advanced Synthesis & Catalysis. 349: 1657-1660. DOI: 10.1002/Adsc.200790022 |
0.587 |
|
| 2006 |
You S, Dai L. Enantioselektive Palladium‐katalysierte decarboxylierende allylische Alkylierungen Angewandte Chemie. 118: 5372-5374. DOI: 10.1002/Ange.200601889 |
0.491 |
|
| 2005 |
Deechongkit S, Powers ET, You SL, Kelly JW. Controlling the morphology of cross beta-sheet assemblies by rational design. Journal of the American Chemical Society. 127: 8562-70. PMID 15941292 DOI: 10.1021/Ja050558C |
0.757 |
|
| 2005 |
You S, Kelly JW. Total synthesis of didmolamides A and B Tetrahedron Letters. 46: 2567-2570. DOI: 10.1016/J.Tetlet.2005.02.097 |
0.661 |
|
| 2005 |
You S, Kelly JW. The total synthesis of bistratamides F–I Tetrahedron. 61: 241-249. DOI: 10.1016/J.Tet.2004.10.024 |
0.719 |
|
| 2005 |
Hou XL, You SL, Tu T, Deng WP, Wu XW, Li M, Yuan K, Zhang TZ, Dai LX. Enantioselective Transition-Metal Catalyzed Carbon–Carbon Bond Formation Reactions using Novel Chiral Ferrocenes and Cyclophanes Topics in Catalysis. 35: 87-103. DOI: 10.1007/s11244-005-3815-3 |
0.388 |
|
| 2004 |
You SL, Deechongkit S, Kelly JW. Solid-phase synthesis and stereochemical assignments of tenuecyclamides A-D employing heterocyclic amino acids derived from commercially available Fmoc alpha-amino acids. Organic Letters. 6: 2627-30. PMID 15255707 DOI: 10.1021/Ol049020M |
0.812 |
|
| 2004 |
You SL, Kelly JW. Highly efficient enantiospecific synthesis of imidazoline-containing amino acids using bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate. Organic Letters. 6: 1681-3. PMID 15128266 DOI: 10.1021/Ol049439C |
0.62 |
|
| 2004 |
Deechongkit S, You SL, Kelly JW. Synthesis of all nineteen appropriately protected chiral alpha-hydroxy acid equivalents of the alpha-amino acids for Boc solid-phase depsi-peptide synthesis. Organic Letters. 6: 497-500. PMID 14961607 DOI: 10.1021/Ol036102M |
0.798 |
|
| 2004 |
You SL, Kelly JW. Highly efficient biomimetic total synthesis and structural verification of bistratamides E and J from Lissoclinum bistratum. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 71-5. PMID 14695551 DOI: 10.1002/Chem.200305504 |
0.643 |
|
| 2003 |
You SL, Razavi H, Kelly JW. A biomimetic synthesis of thiazolines using hexaphenyloxodiphosphonium trifluoromethanesulfonate. Angewandte Chemie (International Ed. in English). 42: 83-5. PMID 19757597 DOI: 10.1002/Anie.200390059 |
0.694 |
|
| 2003 |
You SL, Kelly JW. Total synthesis of dendroamide a: oxazole and thiazole construction using an oxodiphosphonium salt. The Journal of Organic Chemistry. 68: 9506-9. PMID 14629183 DOI: 10.1021/Jo0302657 |
0.693 |
|
| 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 |
0.675 |
|
| 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 |
0.659 |
|
| 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 |
0.623 |
|
| 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 |
0.698 |
|
| 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 |
0.683 |
|
| 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 |
0.67 |
|
| 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 |
0.63 |
|
| 2000 |
You S, Hou X, Dai L, Cao B, Sun J. Novel Bis-N-[2-(diphenylphosphino)ferrocenylcarbonyl]-diaminocyclohexane ligands: application in asymmetric allylic alkylation of imino ester with simple allyl carbonate Chemical Communications. 1933-1934. DOI: 10.1039/B003804K |
0.695 |
|
| 2000 |
You S, Hou X, Dai L. Synthesis of planar chiral selenide derivatives of ferrocenyl-oxazoline and their application in enantioselective palladium catalyzed allylic substitution reaction Tetrahedron: Asymmetry. 11: 1495-1500. DOI: 10.1016/S0957-4166(00)00078-1 |
0.767 |
|
| 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 |
0.75 |
|
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