| Year |
Citation |
Score |
| 2024 |
Jiao Y, Shi X, Ju L, Yu S. Photoredox-Catalyzed Synthesis of -Benzoselenazolyl/Benzothiazolyl Glycosides from 2-Isocyanoaryl Selenoethers/Thioethers and Glycosyl Bromides. Organic Letters. PMID 38165656 DOI: 10.1021/acs.orglett.3c04059 |
0.604 |
|
| 2023 |
Tang S, Zhang HH, Yu S. Enantioselective reductive allylic alkylation enabled by dual photoredox/palladium catalysis. Chemical Communications (Cambridge, England). PMID 36628922 DOI: 10.1039/d2cc06705f |
0.353 |
|
| 2022 |
Zhang H, Huang C, Yuan XA, Yu S. Photoexcited Chiral Copper Complex-Mediated Alkene → Isomerization Enables Kinetic Resolution. Journal of the American Chemical Society. PMID 35675512 DOI: 10.1021/jacs.2c04040 |
0.302 |
|
| 2021 |
Xia L, Jin M, Jiao Y, Yu S. Synthesis of -Alkynyl Glycosides by Photoredox-Catalyzed Reductive Coupling of Alkynyl Bromides with Glycosyl Bromides. Organic Letters. PMID 34941274 DOI: 10.1021/acs.orglett.1c04041 |
0.321 |
|
| 2021 |
Bai X, Qian L, Zhang HH, Yu S. Enantioselective Radical S2-Type Alkylation of Morita-Baylis-Hillman Adducts Using Dual Photoredox/Palladium Catalysis. Organic Letters. 23: 8322-8326. PMID 34672603 DOI: 10.1021/acs.orglett.1c03064 |
0.34 |
|
| 2021 |
Zhang HH, Tang M, Zhao JJ, Song C, Yu S. Enantioselective Reductive Homocoupling of Allylic Acetates Enabled by Dual Photoredox/Palladium Catalysis: Access to -Symmetrical 1,5-Dienes. Journal of the American Chemical Society. PMID 34351745 DOI: 10.1021/jacs.1c06271 |
0.333 |
|
| 2020 |
Zhang H, Wei Z, Zhang AH, Yu S. Access to Cyanoimines Enabled by Dual Photoredox/Copper-Catalyzed Cyanation of -Acyl Oximes. Organic Letters. PMID 32866393 DOI: 10.1021/Acs.Orglett.0C02659 |
0.45 |
|
| 2020 |
Chen H, Jin W, Yu S. Enantioselective Remote C(sp)-H Cyanation via Dual Photoredox and Copper Catalysis. Organic Letters. PMID 32697587 DOI: 10.1021/Acs.Orglett.0C02008 |
0.37 |
|
| 2020 |
Zhang H, Zhao J, Yu S. Enantioselective α-Allylation of Anilines Enabled by a Combined Palladium and Photoredox Catalytic System Acs Catalysis. 10: 4710-4716. DOI: 10.1021/Acscatal.0C00871 |
0.389 |
|
| 2020 |
Shen X, Qian L, Yu S. Photoredox/palladium-cocatalyzed enantioselective alkylation of secondary benzyl carbonates with 4-alkyl-1,4-dihydropyridines Science China Chemistry. 63: 687-691. DOI: 10.1007/S11426-019-9732-5 |
0.413 |
|
| 2020 |
Zhang H, Chen H, Zhu C, Yu S. A review of enantioselective dual transition metal/photoredox catalysis Science China Chemistry. 63: 637-647. DOI: 10.1007/S11426-019-9701-5 |
0.359 |
|
| 2019 |
Li Z, Tang M, Hu C, Yu S. Atroposelective Haloamidation of Indoles with Amino Acid Derivatives and Hypohalides. Organic Letters. PMID 31638398 DOI: 10.1021/Acs.Orglett.9B03456 |
0.419 |
|
| 2019 |
Chen H, Fan W, Yuan XA, Yu S. Site-selective remote C(sp)-H heteroarylation of amides via organic photoredox catalysis. Nature Communications. 10: 4743. PMID 31628325 DOI: 10.1038/S41467-019-12722-4 |
0.35 |
|
| 2019 |
Li Z, Zhang H, Yu S. NaClO-Promoted Atroposelective Couplings of 3-Substituted Indoles with Amino Acid Derivatives. Organic Letters. PMID 31179703 DOI: 10.1021/Acs.Orglett.9B01638 |
0.394 |
|
| 2019 |
Zhang HH, Yu S. Visible-Light-Induced Radical Acylation of Imines with α-Ketoacids Enabled by Electron-Donor-Acceptor Complexes. Organic Letters. 21: 3711-3715. PMID 31066560 DOI: 10.1021/Acs.Orglett.9B01169 |
0.382 |
|
| 2019 |
Zhao JJ, Zhang HH, Shen X, Yu S. Enantioselective Radical Hydroacylation of Enals with α-Ketoacids Enabled by Photoredox/Amine Cocatalysis. Organic Letters. PMID 30694064 DOI: 10.1021/Acs.Orglett.8B03840 |
0.382 |
|
| 2019 |
Dai J, Lu D, Ye T, Yu S, Cheng X. Experimenting with a Suzuki–Miyaura Cross-Coupling Reaction That Demonstrates Tolerance toward Aldehyde Groups To Teach Undergraduate Students the Fundamentals of Transition-Metal-Catalyzed Reactions Journal of Chemical Education. 96: 2672-2675. DOI: 10.1021/Acs.Jchemed.9B00191 |
0.399 |
|
| 2019 |
Zhang H, Xu Q, Yu L, Yu S. Photocatalytic Isomerization of Styrenyl Halides: Stereodivergent Synthesis of Functionalized Alkenes European Journal of Organic Chemistry. 2020: 1472-1477. DOI: 10.1002/Ejoc.201901119 |
0.443 |
|
| 2018 |
Zhang HH, Zhao JJ, Yu S. Enantioselective Allylic Alkylation with 4-Alkyl-1,4-dihydropyridines Enabled by Photoredox/Palladium Cocatalysis. Journal of the American Chemical Society. PMID 30475614 DOI: 10.1021/Jacs.8B10766 |
0.476 |
|
| 2018 |
Chen H, Guo L, Yu S. Primary, Secondary, and Tertiary γ-C(sp)-H Vinylation of Amides via Organic Photoredox-Catalyzed Hydrogen Atom Transfer. Organic Letters. PMID 30246537 DOI: 10.1021/Acs.Orglett.8B02737 |
0.336 |
|
| 2018 |
Shen X, Zhao JJ, Yu S. Photoredox-Catalyzed Intermolecular Remote C-H and C-C Vinylation via Iminyl Radicals. Organic Letters. PMID 30136853 DOI: 10.1021/Acs.Orglett.8B02540 |
0.315 |
|
| 2018 |
An XD, Jiao YY, Zhang H, Gao Y, Yu S. Photoredox-Induced Radical Relay toward Functionalized β-Amino Alcohol Derivatives. Organic Letters. PMID 29314850 DOI: 10.1021/Acs.Orglett.7B03693 |
0.389 |
|
| 2018 |
Yu S, An X. Photoredox-Catalyzed Radical Relay Reaction Toward Functionalized Vicinal Diamines Synthesis. 50: 3387-3394. DOI: 10.1055/S-0037-1609844 |
0.409 |
|
| 2018 |
Wang H, Xu Q, Yu S. Visible light-induced aryltrifluoromethylation of hydroxy alkenes via radical trifluoromethylation-triggered aryl and heteroaryl migration Organic Chemistry Frontiers. 5: 2224-2228. DOI: 10.1039/C8Qo00430G |
0.39 |
|
| 2018 |
Sun J, He Y, An X, Zhang X, Yu L, Yu S. Visible-light-induced iminyl radical formation via electron-donor–acceptor complexes: a photocatalyst-free approach to phenanthridines and quinolines Organic Chemistry Frontiers. 5: 977-981. DOI: 10.1039/C7Qo00992E |
0.313 |
|
| 2018 |
An X, Yu S. Photoredox-catalyzed C(sp2)–N coupling reactions Tetrahedron Letters. 59: 1605-1613. DOI: 10.1016/J.Tetlet.2018.03.050 |
0.338 |
|
| 2018 |
Sun X, He Y, Yu S. Halogen-bond-mediated atom transfer radical addition of perfluoroalkyl iodides to alkynes under visible light irradiation Journal of Photochemistry and Photobiology a: Chemistry. 355: 326-331. DOI: 10.1016/J.Jphotochem.2017.08.026 |
0.351 |
|
| 2018 |
An X, Zhang H, Xu Q, Yu L, Yu S. Stereodivergent Synthesis of α-Aminomethyl Cinnamyl Ethers via
Photoredox-Catalyzed Radical Relay Reaction Chinese Journal of Chemistry. 36: 1147-1150. DOI: 10.1002/Cjoc.201800387 |
0.449 |
|
| 2017 |
Zhang M, Li N, Tao X, Ruzi R, Yu S, Zhu C. Selective reduction of carboxylic acids to aldehydes with hydrosilane via photoredox catalysis. Chemical Communications (Cambridge, England). PMID 28861564 DOI: 10.1039/C7Cc05570F |
0.413 |
|
| 2017 |
Zhang HH, Yu S. Radical Alkylation of Imines with 4-Alkyl-1,4-dihydropyridines Enabled by Photoredox/Brønsted Acid Co-catalysis. The Journal of Organic Chemistry. PMID 28825289 DOI: 10.1021/Acs.Joc.7B01425 |
0.477 |
|
| 2017 |
Zhang M, Ruzi R, Xi J, Li N, Wu Z, Li W, Yu S, Zhu C. Photoredox-Catalyzed Hydroacylation of Olefins Employing Carboxylic Acids and Hydrosilanes. Organic Letters. PMID 28612606 DOI: 10.1021/Acs.Orglett.7B01391 |
0.42 |
|
| 2017 |
Qin Q, Han YY, Jiao YY, He Y, Yu S. Photoredox-Catalyzed Diamidation and Oxidative Amidation of Alkenes: Solvent-Enabled Synthesis of 1,2-Diamides and α-Amino Ketones. Organic Letters. PMID 28508648 DOI: 10.1021/Acs.Orglett.7B01145 |
0.467 |
|
| 2017 |
Jiang H, He Y, Cheng Y, Yu S. Radical Alkynyltrifluoromethylation of Alkenes Initiated by an Electron Donor-Acceptor Complex. Organic Letters. PMID 28207267 DOI: 10.1021/Acs.Orglett.7B00337 |
0.407 |
|
| 2017 |
Qin Q, Jiang H, Hu Z, Ren D, Yu S. Functionalization of C-H Bonds by Photoredox Catalysis. Chemical Record (New York, N.Y.). PMID 28074599 DOI: 10.1002/Tcr.201600125 |
0.321 |
|
| 2016 |
Cheng J, Li W, Duan Y, Cheng Y, Yu S, Zhu C. Relay Visible-Light Photoredox Catalysis: Synthesis of Pyrazole Derivatives via Formal [4 + 1] Annulation and Aromatization. Organic Letters. PMID 27996274 DOI: 10.1021/Acs.Orglett.6B03497 |
0.448 |
|
| 2016 |
Wang H, Xu Q, Shen S, Yu S. Synthesis of Quinolines through Three-Component Cascade Annulation of Aryl Diazonium Salts, Nitriles, and Alkynes. The Journal of Organic Chemistry. PMID 27936733 DOI: 10.1021/Acs.Joc.6B02509 |
0.489 |
|
| 2016 |
Zhang M, Duan Y, Li W, Xu P, Cheng J, Yu S, Zhu C. A Single Electron Transfer (SET) Approach to C-H Amidation of Hydrazones via Visible-Light Photoredox Catalysis. Organic Letters. PMID 27689817 DOI: 10.1021/Acs.Orglett.6B02711 |
0.329 |
|
| 2016 |
Tong K, Liu X, Zhang Y, Yu S. Visible-Light-Induced Direct Oxidative CH Amidation of Heteroarenes with Sulfonamides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27599166 DOI: 10.1002/Chem.201604014 |
0.339 |
|
| 2016 |
Sun X, Wang W, Li Y, Ma J, Yu S. Halogen-Bond-Promoted Double Radical Isocyanide Insertion under Visible-Light Irradiation: Synthesis of 2-Fluoroalkylated Quinoxalines. Organic Letters. PMID 27579571 DOI: 10.1021/Acs.Orglett.6B02271 |
0.336 |
|
| 2016 |
Sun X, Yu S. Visible-light-promoted iminyl radical formation from vinyl azides: synthesis of 6-(fluoro)alkylated phenanthridines. Chemical Communications (Cambridge, England). PMID 27530901 DOI: 10.1039/C6Cc05756J |
0.486 |
|
| 2016 |
Han YY, Jiang H, Wang R, Yu S. Synthesis of Tetracyclic Quinazolinones Using a Visible-Light-Promoted Radical Cascade Approach. The Journal of Organic Chemistry. PMID 27257828 DOI: 10.1021/Acs.Joc.6B00869 |
0.394 |
|
| 2016 |
Zhou H, Deng X, Ma Z, Zhang A, Qin Q, Tan RX, Yu S. Synthesis of furo[3,2-c]coumarin derivatives using visible-light-promoted radical alkyne insertion with bromocoumarins. Organic & Biomolecular Chemistry. PMID 27241337 DOI: 10.1039/C6Ob00768F |
0.406 |
|
| 2016 |
Cheng Y, Yu S. Hydrotrifluoromethylation of Unactivated Alkenes and Alkynes Enabled by an Electron-Donor-Acceptor Complex of Togni's Reagent with a Tertiary Amine. Organic Letters. PMID 27227431 DOI: 10.1021/Acs.Orglett.6B01301 |
0.322 |
|
| 2016 |
Yu S, Sun X. Visible-Light-Promoted and Photoredox-Catalyzed Radical Addition to Triple Bonds Synlett. 27: 2659-2675. DOI: 10.1055/S-0036-1588631 |
0.481 |
|
| 2016 |
Han Y, Wang H, Yu S. Synthesis of biaryl sultams using visible-light-promoted denitrogenative cyclization of 1,2,3,4-benzothiatriazine-1,1-dioxides Organic Chemistry Frontiers. 3: 953-956. DOI: 10.1039/C6Qo00116E |
0.379 |
|
| 2016 |
Wang H, Cheng Y, Yu S. Visible-light-promoted and photocatalyst-free trifluoromethylation of enamides Science China Chemistry. 59: 195-198. DOI: 10.1007/S11426-015-5528-1 |
0.378 |
|
| 2016 |
Han Y, Wang H, Yu S. ChemInform Abstract: Synthesis of Biaryl Sultams Using Visible-Light-Promoted Denitrogenative Cyclization of 1,2,3,4-Benzothiatriazine-1,1-dioxides. Cheminform. 47. DOI: 10.1002/CHIN.201649175 |
0.305 |
|
| 2016 |
Tong K, Zheng T, Zhang Y, Yu S. ChemInform Abstract: Synthesis of ortho-(Fluoro)alkylated Pyridines via Visible Light-Promoted Radical Isocyanide Insertion. Cheminform. 47. DOI: 10.1002/CHIN.201614141 |
0.328 |
|
| 2016 |
Han Y, Jiao Y, Ren D, Hu Z, Shen S, Yu S. Synthesis of Tetrasubstituted Furans by Using Photoredox‐Catalyzed Coupling of 2‐Bromo‐1,3‐dicarbonyl Compounds with Silyl Enol Ethers Asian Journal of Organic Chemistry. 6: 414-417. DOI: 10.1002/Ajoc.201600489 |
0.493 |
|
| 2015 |
An XD, Yu S. Direct Synthesis of Nitriles from Aldehydes Using an O-Benzoyl Hydroxylamine (BHA) as the Nitrogen Source. Organic Letters. PMID 26418564 DOI: 10.1021/Acs.Orglett.5B02547 |
0.413 |
|
| 2015 |
Qin Q, Ren D, Yu S. Visible-light-promoted chloramination of olefins with N-chlorosulfonamide as both nitrogen and chlorine sources. Organic & Biomolecular Chemistry. PMID 26416235 DOI: 10.1039/C5Ob01725D |
0.417 |
|
| 2015 |
Wang H, Yu S. Synthesis of Isoquinolones Using Visible-Light-Promoted Denitrogenative Alkyne Insertion of 1,2,3-Benzotriazinones. Organic Letters. PMID 26291343 DOI: 10.1021/Acs.Orglett.5B01960 |
0.407 |
|
| 2015 |
An XD, Yu S. Visible-light-promoted and one-pot synthesis of phenanthridines and quinolines from aldehydes and O-acyl hydroxylamine. Organic Letters. 17: 2692-5. PMID 25964987 DOI: 10.1021/Acs.Orglett.5B01096 |
0.399 |
|
| 2015 |
Cheng Y, Yuan X, Ma J, Yu S. Direct Aromatic CH Trifluoromethylation via an Electron-Donor-Acceptor Complex. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8355-9. PMID 25907421 DOI: 10.1002/Chem.201500896 |
0.335 |
|
| 2015 |
Qin Q, Yu S. Visible-light-promoted remote C(sp(3))-H amidation and chlorination. Organic Letters. 17: 1894-7. PMID 25853884 DOI: 10.1021/Acs.Orglett.5B00582 |
0.342 |
|
| 2015 |
Jiang H, An X, Tong K, Zheng T, Zhang Y, Yu S. Visible-light-promoted iminyl-radical formation from acyl oximes: a unified approach to pyridines, quinolines, and phenanthridines. Angewandte Chemie (International Ed. in English). 54: 4055-9. PMID 25650356 DOI: 10.1002/Anie.201411342 |
0.452 |
|
| 2015 |
Guo J, Yu S. Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation. Organic & Biomolecular Chemistry. 13: 1179-86. PMID 25428596 DOI: 10.1039/C4Ob02227K |
0.471 |
|
| 2015 |
Sun X, Li J, Ni Y, Ren D, Hu Z, Yu S. ChemInform Abstract: Synthesis of Fused Quinoline and Quinoxaline Derivatives Enabled by Domino Radical Triple Bond Insertions. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201520190 |
0.303 |
|
| 2015 |
Wang R, Jiang H, Cheng Y, Kadi AA, Fun H, Zhang Y, Yu S. ChemInform Abstract: Somophilic Isocyanide Insertion: Synthesis of 6-Arylated and 6-Trifluoromethylated Phenanthridines. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201514217 |
0.397 |
|
| 2015 |
Cheng Y, Yuan X, Jiang H, Wang R, Ma J, Zhang Y, Yu S. ChemInform Abstract: Regiospecific Synthesis of 1-Trifluoromethylisoquinolines Enabled by Photoredox Somophilic Vinyl Isocyanide Insertion. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201511217 |
0.367 |
|
| 2015 |
Tong K, Zheng T, Zhang Y, Yu S. Synthesis of ortho-(Fluoro)alkylated Pyridines via Visible Light-Promoted Radical Isocyanide Insertion Advanced Synthesis and Catalysis. 357: 3681-3686. DOI: 10.1002/Adsc.201500674 |
0.457 |
|
| 2014 |
Cheng S, Yu S. Enantioselective synthesis of 3-substituted 1,2-oxazinanes via organocatalytic intramolecular aza-Michael addition. Organic & Biomolecular Chemistry. 12: 8607-10. PMID 25272305 DOI: 10.1039/C4Ob01646G |
0.466 |
|
| 2014 |
Qin Q, Yu S. Visible-light-promoted redox neutral C-H amidation of heteroarenes with hydroxylamine derivatives Organic Letters. 16: 3504-3507. PMID 24964153 DOI: 10.1021/Ol501457S |
0.411 |
|
| 2014 |
Sun X, Yu S. Visible-light-mediated fluoroalkylation of isocyanides with ethyl bromofluoroacetates: unified synthesis of mono- and difluoromethylated phenanthridine derivatives. Organic Letters. 16: 2938-41. PMID 24850129 DOI: 10.1021/Ol501081H |
0.467 |
|
| 2014 |
Jiang H, Cheng Y, Wang R, Zhang Y, Yu S. Synthesis of isoquinolines via visible light-promoted insertion of vinyl isocyanides with diaryliodonium salts. Chemical Communications (Cambridge, England). 50: 6164-7. PMID 24776694 DOI: 10.1039/C4Cc01122H |
0.44 |
|
| 2014 |
Guo J, Sun X, Yu S. Diastereoselective synthesis of epoxide-fused benzoquinolizidine derivatives using intramolecular domino aza-Michael addition/Darzens reaction. Organic & Biomolecular Chemistry. 12: 265-8. PMID 24281194 DOI: 10.1039/C3Ob42068J |
0.52 |
|
| 2014 |
Zhang Y, Yu S, Wang R, Jiang H, Cheng Y, Kadi A, Fun H. Somophilic Isocyanide Insertion: Synthesis of 6-Arylated and 6-Trifluoromethylated Phenanthridines Synthesis. 46: 2711-2726. DOI: 10.1055/S-0034-1379217 |
0.493 |
|
| 2014 |
Cheng S, Zhao L, Yu S. ChemInform Abstract: Enantioselective Synthesis of Azaflavanones Using Organocatalytic 6-endo Aza-Michael Addition. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201435167 |
0.407 |
|
| 2014 |
Sun X, Li J, Ni Y, Ren D, Hu Z, Yu S. Synthesis of Fused Quinoline and Quinoxaline Derivatives Enabled by Domino Radical Triple Bond Insertions Asian Journal of Organic Chemistry. 3: 1317-1325. DOI: 10.1002/Ajoc.201402222 |
0.455 |
|
| 2014 |
Cheng Y, Yuan X, Jiang H, Wang R, Ma J, Zhang Y, Yu S. Regiospecific Synthesis of 1-Trifluoromethylisoquinolines Enabled by Photoredox Somophilic Vinyl Isocyanide Insertion Advanced Synthesis & Catalysis. 356: 2859-2866. DOI: 10.1002/Adsc.201400504 |
0.447 |
|
| 2014 |
Cheng S, Zhao L, Yu S. Enantioselective Synthesis of Azaflavanones Using Organocatalytic 6-endoAza-Michael Addition Advanced Synthesis & Catalysis. 356: 982-986. DOI: 10.1002/Adsc.201300920 |
0.505 |
|
| 2013 |
Jiang H, Cheng Y, Wang R, Zheng M, Zhang Y, Yu S. Synthesis of 6-alkylated phenanthridine derivatives using photoredox neutral somophilic isocyanide insertion. Angewandte Chemie (International Ed. in English). 52: 13289-92. PMID 24222447 DOI: 10.1002/Anie.201308376 |
0.496 |
|
| 2013 |
Cheng Y, Jiang H, Zhang Y, Yu S. Isocyanide insertion: de novo synthesis of trifluoromethylated phenanthridine derivatives. Organic Letters. 15: 5520-3. PMID 24180686 DOI: 10.1021/Ol4026827 |
0.486 |
|
| 2013 |
Jiang H, Cheng Y, Zhang Y, Yu S. De novo synthesis of polysubstituted naphthols and furans using photoredox neutral coupling of alkynes with 2-bromo-1,3-dicarbonyl compounds. Organic Letters. 15: 4884-7. PMID 24000895 DOI: 10.1021/Ol402325Z |
0.461 |
|
| 2013 |
Liu H, Zeng C, Guo J, Zhang M, Yu S. Enantioselective synthesis of 2-substituted pyrrolidinesvia domino cross metathesis/intramolecular aza-Michael addition Rsc Adv.. 3: 1666-1668. DOI: 10.1039/C2Ra22374K |
0.532 |
|
| 2013 |
Jiang H, Cheng Y, Zhang Y, Yu S. Sulfonation and Trifluoromethylation of Enol Acetates with Sulfonyl Chlorides Using Visible-Light Photoredox Catalysis European Journal of Organic Chemistry. 2013: 5485-5492. DOI: 10.1002/Ejoc.201300693 |
0.391 |
|
| 2013 |
Jiang H, Chen X, Zhang Y, Yu S. CH Functionalization of Enamides: Synthesis of β-Amidovinyl SulfonesviaVisible-Light Photoredox Catalysis Advanced Synthesis & Catalysis. 355: 809-813. DOI: 10.1002/Adsc.201200874 |
0.36 |
|
| 2012 |
Jiang H, Huang C, Guo J, Zeng C, Zhang Y, Yu S. Direct C-H functionalization of enamides and enecarbamates by using visible-light photoredox catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15158-66. PMID 23018775 DOI: 10.1002/Chem.201201716 |
0.422 |
|
| 2012 |
Zhou F, Guo J, Liu J, Ding K, Yu S, Cai Q. Copper-catalyzed desymmetric intramolecular Ullmann C-N coupling: an enantioselective preparation of indolines. Journal of the American Chemical Society. 134: 14326-9. PMID 22913611 DOI: 10.1021/Ja306631Z |
0.673 |
|
| 2012 |
Yu S, Zeng C, Liu H, Zhang M, Guo J, Jiang S. Enantioselective Synthesis of Cryptopleurine and Boehmeriasin A via Organocatalytic Intramolecular Aza-Michael Addition Synlett. 23: 2251-2254. DOI: 10.1055/S-0031-1290457 |
0.516 |
|
| 2011 |
Zi W, Yu S, Ma D. Synthetic studies toward galbulimima alkaloid (-)-GB 13 and (+)-GB 16 and (-)-himgaline. Chemistry, An Asian Journal. 6: 573-9. PMID 21254431 DOI: 10.1002/Asia.201000556 |
0.78 |
|
| 2011 |
Li W, Yu S, Jin M, Xia H, Ma D. Total synthesis and cytotoxicity of bisebromoamide and its analogues Tetrahedron Letters. 52: 2124-2127. DOI: 10.1016/J.Tetlet.2010.11.058 |
0.71 |
|
| 2011 |
Yu S, Zhu S, Pan X, Yang J, Ma D. Reinvestigation on total synthesis of kaitocephalin and its isomers Tetrahedron. 67: 1673-1680. DOI: 10.1016/J.Tet.2010.12.068 |
0.753 |
|
| 2010 |
Juarez-Garcia ME, Yu S, Bode JW. Asymmetric synthesis of enantiopure isoxazolidinone monomers for the synthesis of β-oligopeptides by chemoselective amide ligation. Tetrahedron. 66: 4841-4853. PMID 21499500 DOI: 10.1016/J.Tet.2010.04.016 |
0.584 |
|
| 2010 |
Zi W, Yu S, Ma D. A convergent route to the Galbulimima alkaloids (-)-GB 13 and (+)-GB 16. Angewandte Chemie (International Ed. in English). 49: 5887-90. PMID 20629004 DOI: 10.1002/Anie.201002299 |
0.706 |
|
| 2010 |
Zhu S, Yu S, Wang Y, Ma D. Organocatalytic Michael addition of aldehydes to protected 2-amino-1-nitroethenes: the practical syntheses of oseltamivir (Tamiflu) and substituted 3-aminopyrrolidines. Angewandte Chemie (International Ed. in English). 49: 4656-60. PMID 20480479 DOI: 10.1002/Anie.201001644 |
0.738 |
|
| 2010 |
Yu S, Ishida H, Juarez-Garcia ME, Bode JW. Unified synthesis of enantiopure β2h, β3h and β2,3-amino acids Chemical Science. 1: 637-641. DOI: 10.1039/C0Sc00317D |
0.536 |
|
| 2010 |
Juarez-Garcia ME, Yu S, Bode JW. Asymmetric synthesis of enantiopure isoxazolidinone monomers for the synthesis of β3-oligopeptides by chemoselective amide ligation Tetrahedron. 66: 4841-4853. DOI: 10.1016/j.tet.2010.04.016 |
0.566 |
|
| 2008 |
Zhu S, Yu S, Ma D. Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water. Angewandte Chemie (International Ed. in English). 47: 545-8. PMID 18038442 DOI: 10.1002/Anie.200704161 |
0.715 |
|
| 2007 |
Sun Z, Yu S, Ding Z, Ma D. Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-Bis(oxazoline) complexes. Journal of the American Chemical Society. 129: 9300-1. PMID 17625864 DOI: 10.1021/Ja0734849 |
0.786 |
|
| 2007 |
Yu S, Liu F, Ma D. A Flexible Route to Immunosuppressive Agent FR252921. Asymmetric Total Synthesis of Its (13R,14R,19R)-Isomer. Cheminform. 38. DOI: 10.1002/CHIN.200714219 |
0.423 |
|
| 2006 |
Yu S, Pan X, Ma D. Asymmetric total syntheses of marine cyclic depsipeptide halipeptins A-D. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6572-84. PMID 16847995 DOI: 10.1002/Chem.200600383 |
0.748 |
|
| 2006 |
Yu S, Liu F, Ma D. A flexible route to immunosuppressive agent FR252921. Asymmetric total synthesis of its (13R,14R,19R)-isomer Tetrahedron Letters. 47: 9155-9157. DOI: 10.1016/J.Tetlet.2006.09.169 |
0.547 |
|
| 2006 |
Ma D, Zhu J, Yu S, Pan X. Synthetic Studies Toward Two Marine Cyclic Peptides Cheminform. 37. DOI: 10.1002/chin.200622262 |
0.707 |
|
| 2004 |
Yu S, Pan X, Lin X, Ma D. Total synthesis of halipeptin A: a potent antiinflammatory cyclic depsipeptide. Angewandte Chemie (International Ed. in English). 44: 135-8. PMID 15599918 DOI: 10.1002/Anie.200461239 |
0.759 |
|
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