| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2023 | Huang J, Li T, Lu X, Ma D. Copper-Catalyzed α-Arylation of Nitroalkanes with (Hetero)aryl Bromides/Iodides. Angewandte Chemie (International Ed. in English). e202315994. PMID 38151905 DOI: 10.1002/anie.202315994 | 0.384 | |||
| 2023 | Zhang H, Lin G, Jia S, Zhang Y, Wu J, Tao Y, Huang W, Song M, Ding K, Ma D, Fan M. Discovery and optimization of thieno[3,2-d]pyrimidine derivatives as highly selective inhibitors of cyclin-dependent kinase 7. European Journal of Medicinal Chemistry. 263: 115955. PMID 38000213 DOI: 10.1016/j.ejmech.2023.115955 | 0.409 | |||
| 2023 | Zhang R, Zhou Q, Wang X, Xu L, Ma D. Copper-Catalyzed Asymmetric Arylation of α-Substituted Cyanoacetates Enabled by Chiral Amide Ligands. Angewandte Chemie (International Ed. in English). e202312383. PMID 37870538 DOI: 10.1002/anie.202312383 | 0.354 | |||
| 2023 | Chen Y, Li S, Xu L, Ma D. Cu/Oxalic Diamide-Catalyzed Coupling of Terminal Alkynes with Aryl Halides. The Journal of Organic Chemistry. PMID 36779409 DOI: 10.1021/acs.joc.2c02882 | 0.35 | |||
| 2022 | Li Q, Xu L, Ma D. Cu-Catalyzed Coupling Reactions of Sulfonamides with (Hetero)Aryl Chlorides/Bromides. Angewandte Chemie (International Ed. in English). e202210483. PMID 36066563 DOI: 10.1002/anie.202210483 | 0.333 | |||
| 2022 | Bhunia S, De S, Ma D. Room Temperature Cu-Catalyzed -Arylation of Oxazolidinones and Amides with (Hetero)Aryl Iodides. Organic Letters. 24: 1253-1257. PMID 35099979 DOI: 10.1021/acs.orglett.2c00122 | 0.306 | |||
| 2021 | Gao Y, Ma D. In Pursuit of Synthetic Efficiency: Convergent Approaches. Accounts of Chemical Research. PMID 33448789 DOI: 10.1021/acs.accounts.0c00727 | 0.317 | |||
| 2020 | Ma D, Chen Y, Xu L, Jiang Y. Assembly of α-(Hetero)aryl Nitriles via Cu-Catalyzed Coupling Reactions with (Hetero)aryl Chlorides and Bromides. Angewandte Chemie (International Ed. in English). PMID 33372348 DOI: 10.1002/anie.202014638 | 0.644 | |||
| 2020 | Ma D, Karre N, Ni D. Total synthesis of kopsinitarine E. Angewandte Chemie (International Ed. in English). PMID 32833268 DOI: 10.1002/Anie.202011093 | 0.413 | |||
| 2020 | Wei Q, Wang Y, Zhao J, Zhang X, Ma D. Assembly of 7-carboxylate indoles via the Cu-catalyzed coupling of substituted 2-iodobenzoic acids and substituted hydrazines Tetrahedron. 76: 130794. DOI: 10.1016/J.Tet.2019.130794 | 0.5 | |||
| 2019 | Ma D, Wang J. 6-Methylenebicyclo[3.2.1]oct-1-en-3-one: A twisted olefin as Diels-Alder dienophile for expedite syntheses of four kaurane diterpenoids. Angewandte Chemie (International Ed. in English). PMID 31432578 DOI: 10.1002/Anie.201909349 | 0.438 | |||
| 2019 | Chen Z, Ma D. Cu/,'-Dibenzyloxalamide-Catalyzed -Arylation of Heteroanilines. Organic Letters. PMID 31414821 DOI: 10.1021/Acs.Orglett.9B02509 | 0.437 | |||
| 2019 | Gao Y, Wei Y, Ma D. Synthetic Studies toward Plumisclerin A. Organic Letters. PMID 30767543 DOI: 10.1021/Acs.Orglett.9B00095 | 0.451 | |||
| 2019 | Ma D, He W, Zhang Z. A scalable total synthesis of Et-743 and lurbinectedin. Angewandte Chemie (International Ed. in English). PMID 30689274 DOI: 10.1002/Anie.201900035 | 0.378 | |||
| 2019 | Chen Z, Jiang Y, Zhang L, Guo YL, Ma D. Oxalic diamides and tert-butoxide: Two types of ligands enabling practical access to alkyl aryl ethers via Cu-catalyzed coupling reaction. Journal of the American Chemical Society. PMID 30688450 DOI: 10.1021/Jacs.8B12142 | 0.658 | |||
| 2019 | Li W, Wang J, Ma D. The Total Synthesis of ent-Kaurane Diterpenoids Progress in Chemistry. 31: 1460. DOI: 10.7536/Pc190809 | 0.434 | |||
| 2018 | Nagaraju K, Ma D. Oxidative coupling strategies for the synthesis of indole alkaloids. Chemical Society Reviews. PMID 30221274 DOI: 10.1039/C8Cs00305J | 0.452 | |||
| 2018 | Wang P, Gao Y, Ma D. Divergent entry to gelsedine-type alkaloids: Total syntheses of (-)-gelsedilam, (-)-gelsenicine, (-)-gelsedine and (-)-gelsemoxonine. Journal of the American Chemical Society. PMID 30160105 DOI: 10.1021/Jacs.8B08127 | 0.359 | |||
| 2018 | Ma D, Ni D, Wei Y. Thiourea-catalyzed asymmetric Michael addition of carbazolones to 2-chloroacrylonitrile: Total synthesis of 5,22-dioxokopsane, kopsinidine C and demethoxycarbonylkopsin. Angewandte Chemie (International Ed. in English). PMID 29920902 DOI: 10.1002/Anie.201805905 | 0.493 | |||
| 2018 | Zhao J, Niu S, Jiang X, Jiang Y, Zhang X, Sun T, Ma D. A Class of Amide Ligands Enable Cu-Catalyzed Coupling of (Hetero)aryl Halides with Sulfinic Acid Salts under Mild Conditions. The Journal of Organic Chemistry. PMID 29786439 DOI: 10.1021/Acs.Joc.8B00888 | 0.64 | |||
| 2018 | Ma D, Liu J. A unified approach for the assembly of atisine- and hetidine-type diterpenoid alkaloids: Total syntheses of azitine and the proposed structure of navirine C. Angewandte Chemie (International Ed. in English). PMID 29611891 DOI: 10.1002/Anie.201803018 | 0.51 | |||
| 2018 | Ma D, Gao Y, Fan M, Geng Q. Total Synthesis of Lapidilectine B Enabled by Manganese(III)-Mediated Oxidative Cyclization of Indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29572984 DOI: 10.1002/Chem.201801312 | 0.458 | |||
| 2018 | Kumar SV, Ma D. Synthesis of N-(Hetero)Aryl Carbamates via CuI/MNAO Catalyzed Cross-Coupling of (Hetero)Aryl Halides with Potassium Cyanate in Alcohols. The Journal of Organic Chemistry. PMID 29406714 DOI: 10.1021/Acs.Joc.7B03175 | 0.466 | |||
| 2018 | Kumar SV, Ma D. Synthesis of Aryl Hydrazines via CuI/BMPO Catalyzed Cross-Coupling of Aryl Halides with Hydrazine Hydrate in Water Chinese Journal of Chemistry. 36: 1003-1006. DOI: 10.1002/Cjoc.201800326 | 0.423 | |||
| 2017 | Bhunia S, Kumar SV, Ma D. N,N'-Bisoxalamides Enhance the Catalytic Activity in Cu-Catalyzed Coupling of (Hetero)Aryl Bromides with Anilines and Secondary Amines. The Journal of Organic Chemistry. PMID 29117476 DOI: 10.1021/Acs.Joc.7B02363 | 0.436 | |||
| 2017 | De S, Yin J, Ma D. Copper-Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amides. Organic Letters. PMID 28858514 DOI: 10.1021/Acs.Orglett.7B02326 | 0.491 | |||
| 2017 | Ma D, Bhunia S, Pawar GG, Kumar SV, Jiang Y. Selected Copper-Based Reactions for C-N, C-O, C-S and C-C Bond Formation. Angewandte Chemie (International Ed. in English). PMID 28544319 DOI: 10.1002/Anie.201701690 | 0.664 | |||
| 2017 | Gao J, Bhunia S, Wang K, Gan L, Xia S, Ma D. Discovery of N-(Naphthalen-1-yl)-N'-alkyl Oxalamide Ligands Enables Cu-Catalyzed Aryl Amination with High Turnovers. Organic Letters. PMID 28530100 DOI: 10.1021/Acs.Orglett.7B00901 | 0.437 | |||
| 2017 | Zhai Y, Chen X, Zhou W, Fan M, Lai Y, Ma D. Copper-Catalyzed Diaryl Ether Formation from (Hetero)aryl Halides at Low Catalytic Loadings. The Journal of Organic Chemistry. PMID 28427259 DOI: 10.1021/Acs.Joc.7B00493 | 0.406 | |||
| 2017 | Zhao X, Li W, Wang J, Ma D. A Convergent Route to ent-Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1a,6a-Diacetoxy-ent-kaura-9(11),16-dien-12,15-dione. Journal of the American Chemical Society. PMID 28186744 DOI: 10.1021/Jacs.7B00140 | 0.354 | |||
| 2017 | Xu L, Tan L, Ma D. Rhodium-Catalyzed Regioselective C7-Functionalization of Indole Derivatives with Acrylates by Using an N-Imino Directing Group Synlett. 28: 2839-2844. DOI: 10.1055/S-0036-1588530 | 0.441 | |||
| 2017 | Ma D, Niu S, Zhao J, Jiang X, Jiang Y, Zhang X, Sun T. A New Class of Amide Ligands Enable Cu‐Catalyzed Coupling of Sodium Methanesulfinate with (Hetero)aryl Chlorides Chinese Journal of Chemistry. 35: 1661-1664. DOI: 10.1002/Cjoc.201700477 | 0.676 | |||
| 2017 | Bhunia S, Pawar GG, Kumar SV, Jiang Y, Ma D. Ausgewählte Kupfer‐katalysierte Reaktionen für die Bildung von C‐N‐, C‐O‐, C‐S‐ und C‐C‐Bindungen Angewandte Chemie. 129: 16352-16397. DOI: 10.1002/Ange.201701690 | 0.497 | |||
| 2017 | Pawar GG, Wu H, De S, Ma D. Copper(I) Oxide/N ,N′ -Bis[(2-furyl)methyl]oxalamide-Catalyzed Coupling of (Hetero)aryl Halides and Nitrogen Heterocycles at Low Catalytic Loading Advanced Synthesis & Catalysis. 359: 1631-1636. DOI: 10.1002/Adsc.201700026 | 0.436 | |||
| 2016 | Wang X, Niu S, Xu L, Zhang C, Meng L, Zhang X, Ma D. Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)-N-Boc-2,6-dimethyltyrosine and Its Analogues. Organic Letters. PMID 28026185 DOI: 10.1021/Acs.Orglett.6B03548 | 0.827 | |||
| 2016 | Xia S, Gan L, Wang K, Li Z, Ma D. Copper-catalyzed hydroxylation of (hetero)aryl halides under mild conditions. Journal of the American Chemical Society. PMID 27682010 DOI: 10.1021/Jacs.6B08114 | 0.413 | |||
| 2016 | Xu L, Tan L, Ma D. Iridium (III)-Catalyzed Regioselective C7-Amination of N-Pivaloylindoles with Sulfonoazides. The Journal of Organic Chemistry. PMID 27572058 DOI: 10.1021/Acs.Joc.6B01856 | 0.442 | |||
| 2016 | Fan M, Zhou W, Jiang Y, Ma D. CuI/Oxalamide Catalyzed Couplings of (Hetero)aryl Chlorides and Phenols for Diaryl Ether Formation. Angewandte Chemie (International Ed. in English). PMID 27072902 DOI: 10.1002/Anie.201601035 | 0.658 | |||
| 2015 | Fan M, Zhou W, Jiang Y, Ma D. Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia. Organic Letters. PMID 26600015 DOI: 10.1021/Acs.Orglett.5B03230 | 0.663 | |||
| 2015 | Xu L, Zhang C, He Y, Tan L, Ma D. Rhodium-Catalyzed Regioselective C7-Functionalization of N-Pivaloylindoles. Angewandte Chemie (International Ed. in English). PMID 26510833 DOI: 10.1002/Anie.201508117 | 0.679 | |||
| 2015 | Zhou W, Fan M, Yin J, Jiang Y, Ma D. CuI/Oxalic Diamide Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amines. Journal of the American Chemical Society. PMID 26352639 DOI: 10.1021/Jacs.5B08411 | 0.685 | |||
| 2015 | Zi W, Zuo Z, Ma D. Intramolecular dearomative oxidative coupling of indoles: a unified strategy for the total synthesis of indoline alkaloids. Accounts of Chemical Research. 48: 702-11. PMID 25667972 DOI: 10.1021/Ar5004303 | 0.833 | |||
| 2015 | He YP, Zhang C, Fan M, Wu Z, Ma D. Assembly of indoline-2-carboxylate-embodied dipeptides via Pd-catalyzed C(sp2)-H bond direct functionalization. Organic Letters. 17: 496-9. PMID 25602435 DOI: 10.1021/Ol503514T | 0.631 | |||
| 2015 | Guo S, Liu J, Ma D. Total synthesis of leucosceptroids A and B. Angewandte Chemie (International Ed. in English). 54: 1298-301. PMID 25470240 DOI: 10.1002/Anie.201410134 | 0.484 | |||
| 2015 | Tian J, Zhong J, Li Y, Ma D. Synthesis of Zanamivir Synfacts. 11: 235-235. DOI: 10.1055/S-0034-1380073 | 0.445 | |||
| 2015 | Zhou Y, Zhang Z, Jiang Y, Pan X, Ma D. Synthesis of 1,2,4-Benzotriazines via Copper(I) Iodide/1 H -Pyrrole-2-carboxylic Acid Catalyzed Coupling of o -Haloacetanilides and N -Boc Hydrazine Synlett. 26: 1586-1590. DOI: 10.1055/S-0034-1378708 | 0.805 | |||
| 2015 | Jiang X, Sun D, Jiang Y, Ma D. Efficient synthesis of pyrrolo[2,3- d ]pyrimidines via a Cu(I)/6-methylpicolinic acid catalyzed coupling reaction Tetrahedron Letters. 56: 3259-3261. DOI: 10.1016/J.Tetlet.2014.12.098 | 0.684 | |||
| 2015 | Zhou Y, Zhang Z, Jiang Y, Pan X, Ma D. ChemInform Abstract: Synthesis of 1,2,4-Benzotriazines via Copper(I) Iodide/1H-Pyrrole-2-carboxylic Acid Catalyzed Coupling of o-Haloacetanilides and N-Boc Hydrazine. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201545190 | 0.796 | |||
| 2015 | Jiang X, Sun D, Jiang Y, Ma D. ChemInform Abstract: Efficient Synthesis of Pyrrolo[2,3-d]pyrimidines via a Cu(I)/6-Methylpicolinic Acid Catalyzed Coupling Reaction Cheminform. 46: no-no. DOI: 10.1002/CHIN.201540186 | 0.624 | |||
| 2014 | Tian J, Zhong J, Li Y, Ma D. Organocatalytic and scalable synthesis of the anti-influenza drugs zanamivir, laninamivir, and CS-8958. Angewandte Chemie (International Ed. in English). 53: 13885-8. PMID 25314609 DOI: 10.1002/Anie.201408138 | 0.404 | |||
| 2014 | Liu H, Jiang G, Pan X, Wan X, Lai Y, Ma D, Xie W. Highly asymmetric bromocyclization of tryptophol: unexpected accelerating effect of DABCO-derived bromine complex. Organic Letters. 16: 1908-11. PMID 24666363 DOI: 10.1021/Ol5004109 | 0.726 | |||
| 2014 | Zhou C, Ma D. A copper-catalyzed coupling reaction of vinyl halides and carbazates: application in the assembly of polysubstituted pyrroles. Chemical Communications (Cambridge, England). 50: 3085-8. PMID 24514455 DOI: 10.1039/C3Cc49724K | 0.529 | |||
| 2014 | Teng M, Zi W, Ma D. Total synthesis of the monoterpenoid indole alkaloid (±)- aspidophylline A Angewandte Chemie - International Edition. 53: 1814-1817. PMID 24481917 DOI: 10.1002/Anie.201310928 | 0.823 | |||
| 2014 | Zhao D, Jiang Y, Ma D. Copper-catalyzed coupling of aryl iodides and tert-butyl β-keto esters: efficient access to α-aryl ketones and α-arylacetic acid tert-butyl esters Tetrahedron. 70: 3327-3332. DOI: 10.1016/J.Tet.2013.10.017 | 0.673 | |||
| 2014 | Zhao D, Jiang Y, Ma D. ChemInform Abstract: Copper-Catalyzed Coupling of Aryl Iodides and tert-Butyl β-Keto Esters: Efficient Access to α-Aryl Ketones and α-Arylacetic Acid tert-Butyl Esters. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201441076 | 0.61 | |||
| 2013 | Wei Y, Zhao D, Ma D. Total synthesis of the indole alkaloid (±)- and (+)-methyl N-decarbomethoxychanofruticosinate. Angewandte Chemie (International Ed. in English). 52: 12988-91. PMID 24258849 DOI: 10.1002/Anie.201307788 | 0.464 | |||
| 2013 | Xie W, Jiang G, Liu H, Hu J, Pan X, Zhang H, Wan X, Lai Y, Ma D. Highly enantioselective bromocyclization of tryptamines and its application in the synthesis of (-)-chimonanthine. Angewandte Chemie (International Ed. in English). 52: 12924-7. PMID 24123660 DOI: 10.1002/Anie.201306774 | 0.718 | |||
| 2013 | Fan M, Ma D. Palladium-catalyzed direct functionalization of 2-aminobutanoic acid derivatives: application of a convenient and versatile auxiliary. Angewandte Chemie (International Ed. in English). 52: 12152-5. PMID 24115453 DOI: 10.1002/Anie.201306583 | 0.392 | |||
| 2013 | Zhang P, Yang X, Zhang F, Gabelli SB, Wang R, Zhang Y, Bhat S, Chen X, Furlani M, Amzel LM, Liu JO, Ma D. Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1. Bioorganic & Medicinal Chemistry. 21: 2600-17. PMID 23507151 DOI: 10.1016/J.Bmc.2013.02.023 | 0.361 | |||
| 2013 | Xu L, Peng Y, Pan Q, Jiang Y, Ma D. Assembly of substituted 3-aminoindazoles from 2-bromobenzonitrile via a CuBr-catalyzed coupling/condensation cascade process. The Journal of Organic Chemistry. 78: 3400-4. PMID 23448680 DOI: 10.1021/Jo400071H | 0.675 | |||
| 2013 | Xie W, Zuo Z, Zi W, Ma D. Intramolecular Oxidative Coupling: Applications in Synthesis of Complex Indole Akaloid Scaffolds Chinese Journal of Organic Chemistry. 33: 869. DOI: 10.6023/Cjoc201301035 | 0.821 | |||
| 2013 | Chen Y, Lu Y, Zou Q, Chen H, Ma D. A Scalable Process to the Key Intermediate of Cilazapril, (S)-1-Benzyloxycarbonylhexahydropyridazine-3-carboxylic Acid, Through a Novel Cascade Course Organic Process Research & Development. 17: 1209-1213. DOI: 10.1021/Op400155U | 0.373 | |||
| 2013 | Xie W, Wang H, Fan F, Tian J, Zuo Z, Zi W, Gao K, Ma D. Diastereoselective construction of continuous all-carbon quaternary centers via intramolecular oxidative coupling reaction Tetrahedron Letters. 54: 4392-4396. DOI: 10.1016/J.Tetlet.2013.05.146 | 0.82 | |||
| 2013 | Xie S, Qin P, Li M, Zhang X, Jiang Y, Ma D. Synthesis of 2-alkyl-2-arylcyanoacetates via CuI/sodium picolinate-catalyzed direct arylation of α-substituted cyanoacetates Tetrahedron Letters. 54: 3889-3891. DOI: 10.1016/J.Tetlet.2013.05.057 | 0.672 | |||
| 2013 | Yin H, Chen B, Zhang X, Yang X, Zhang Y, Jiang Y, Ma D. Assembly of N,N-disubstituted-N′-arylureas via a copper-catalyzed one-pot three-component reaction of aryl bromides, potassium cyanate, and secondary amines Tetrahedron. 69: 5326-5330. DOI: 10.1016/J.Tet.2013.04.117 | 0.674 | |||
| 2013 | Yin H, Chen B, Zhang X, Yang X, Zhang Y, Jiang Y, Ma D. ChemInform Abstract: Assembly of N,N-Disubstituted-N′-arylureas via a Copper-Catalyzed One-Pot Three-Component Reaction of Aryl Bromides, Potassium Cyanate, and Secondary Amines. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201345082 | 0.605 | |||
| 2013 | Xie S, Qin P, Li M, Zhang X, Jiang Y, Ma D. ChemInform Abstract: Synthesis of 2-Alkyl-2-arylcyanoacetates via Cul/Sodium Picolinate-Catalyzed Direct Arylation of α-Substituted Cyanoacetates. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201342063 | 0.639 | |||
| 2013 | Wang L, Zhang X, Ma D. ChemInform Abstract: Organocatalytic Michael Addition of Aldehydes to Trisubstituted Nitroolefins. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201307057 | 0.326 | |||
| 2013 | Zhang Y, Xing H, Xie W, Wan X, Lai Y, Ma D. Asymmetric, Regioselective Bromohydroxylation of 2-Aryl-2-propen-1-ols Catalyzed by Quinine-Derived Catalysts Advanced Synthesis & Catalysis. 355: 68-72. DOI: 10.1002/Adsc.201200782 | 0.71 | |||
| 2012 | Tian S, Zi W, Ma D. Potentially biomimetic total synthesis and relative stereochemical assignment of (±)-gracilamine. Angewandte Chemie (International Ed. in English). 51: 10141-4. PMID 22961744 DOI: 10.1002/Anie.201205711 | 0.746 | |||
| 2012 | Fan F, Xie W, Ma D. Cascade annulation of malonic diamides: a concise synthesis of polycyclic pyrroloindolines. Chemical Communications (Cambridge, England). 48: 7571-3. PMID 22728323 DOI: 10.1039/C2Cc33129B | 0.757 | |||
| 2012 | Zhang Y, Yang X, Yao Q, Ma D. CuI/DMPAO-catalyzed N-arylation of acyclic secondary amines. Organic Letters. 14: 3056-9. PMID 22662962 DOI: 10.1021/Ol301135C | 0.442 | |||
| 2012 | Xing H, Zhang Y, Lai Y, Jiang Y, Ma D. Synthesis of symmetrical and unsymmetrical N,N'-diaryl guanidines via copper/N-methylglycine-catalyzed arylation of guanidine nitrate. The Journal of Organic Chemistry. 77: 5449-53. PMID 22655905 DOI: 10.1021/Jo300840X | 0.639 | |||
| 2012 | Zi W, Xie W, Ma D. Total synthesis of Akuammiline alkaloid (-)-vincorine via intramolecular oxidative coupling. Journal of the American Chemical Society. 134: 9126-9. PMID 22616754 DOI: 10.1021/Ja303602F | 0.834 | |||
| 2012 | Xiong X, Jiang Y, Ma D. Assembly of N,N-disubstituted hydrazines and 1-aryl-1H-indazoles via copper-catalyzed coupling reactions. Organic Letters. 14: 2552-5. PMID 22545771 DOI: 10.1021/Ol300847V | 0.802 | |||
| 2012 | Fan F, Xie W, Ma D. Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process. Organic Letters. 14: 1405-7. PMID 22400980 DOI: 10.1021/Ol3003496 | 0.725 | |||
| 2012 | Xu L, Jiang Y, Ma D. Synthesis of 3-substituted and 2,3-disubstituted quinazolinones via Cu-catalyzed aryl amidation. Organic Letters. 14: 1150-3. PMID 22313025 DOI: 10.1021/Ol300084V | 0.687 | |||
| 2012 | Yuan J, Vakifahmetoglu-Norberg H, Xia H, Liu J, Li Y, Kim M, Ma D. Abstract SY36-03: Development of small-molecule inhibitors of autophagy as anticancer therapy Cancer Research. 72. DOI: 10.1158/1538-7445.Am2012-Sy36-03 | 0.611 | |||
| 2012 | Li J, Zhang Y, Jiang Y, Ma D. CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides Tetrahedron Letters. 53: 3981-3983. DOI: 10.1016/J.Tetlet.2012.05.081 | 0.646 | |||
| 2012 | Li J, Zhang Y, Jiang Y, Ma D. CuI-catalyzed one-pot synthesis of benzothiazolones from 2-iodoanilines-derived carbamates and sodium sulfide Tetrahedron Letters. 53: 2511-2513. DOI: 10.1016/J.Tetlet.2012.03.006 | 0.672 | |||
| 2012 | Wang L, Zhang X, Ma D. Organocatalytic Michael addition of aldehydes to trisubstituted nitroolefins Tetrahedron. 68: 7675-7679. DOI: 10.1016/J.Tet.2012.05.088 | 0.473 | |||
| 2012 | Yang X, Xing H, Zhang Y, Lai Y, Zhang Y, Jiang Y, Ma D. CuI/8-Hydroxyquinalidine Promoted N-Arylation of Indole and Azoles Chinese Journal of Chemistry. 30: 875-880. DOI: 10.1002/Cjoc.201100433 | 0.659 | |||
| 2012 | Li J, Zhang Y, Jiang Y, Ma D. ChemInform Abstract: CuI/N,N-Dimethylglycine-Catalyzed Synthesis of N-Aryloxazolidinones from Aryl Bromides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201244120 | 0.572 | |||
| 2012 | Li J, Zhang Y, Jiang Y, Ma D. ChemInform Abstract: CuI-Catalyzed One-Pot Synthesis of Benzothiazolones from 2-Iodoaniline-Derived Carbamates and Sodium Sulfide. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201235139 | 0.657 | |||
| 2012 | Yang X, Zhang Y, Ma D. Synthesis of Aryl Carbamates via Copper-Catalyzed Coupling of Aryl Halides with Potassium Cyanate Advanced Synthesis & Catalysis. 354: 2443-2446. DOI: 10.1002/Adsc.201200296 | 0.465 | |||
| 2012 | Huo L, Ma A, Zhang Y, Ma D. Assembly of 4-Substituted 3-Nitro-1,2,3,4-tetrahydropyridines via Organocatalytic Michael Addition Advanced Synthesis & Catalysis. 354: 991-994. DOI: 10.1002/Adsc.201100903 | 0.36 | |||
| 2011 | Ma D, Jiang Y. Cu((i))/amino acid catalyzed coupling reactions of aryl halides and nucleophiles: applications in large-scale production. Chimia. 65: 914-8. PMID 22273372 DOI: 10.2533/Chimia.2011.914 | 0.665 | |||
| 2011 | Diao X, Xu L, Zhu W, Jiang Y, Wang H, Guo Y, Ma D. The N-aryl aminocarbonyl ortho-substituent effect in Cu-catalyzed aryl amination and its application in the synthesis of 5-substituted 11-oxo-dibenzodiazepines. Organic Letters. 13: 6422-5. PMID 22087816 DOI: 10.1021/Ol202721H | 0.688 | |||
| 2011 | Zuo Z, Ma D. Enantioselective total syntheses of communesins A and B Angewandte Chemie - International Edition. 50: 12008-12011. PMID 22006672 DOI: 10.1002/Anie.201106205 | 0.686 | |||
| 2011 | Liu J, Xia H, Kim M, Xu L, Li Y, Zhang L, Cai Y, Norberg HV, Zhang T, Furuya T, Jin M, Zhu Z, Wang H, Yu J, Li Y, ... ... Ma D, et al. Beclin1 controls the levels of p53 by regulating the deubiquitination activity of USP10 and USP13. Cell. 147: 223-34. PMID 21962518 DOI: 10.1016/J.Cell.2011.08.037 | 0.606 | |||
| 2011 | Sun X, Ma D. Organocatalytic approach for the syntheses of corynantheidol, dihydrocorynantheol, protoemetinol, protoemetine, and mitragynine. Chemistry, An Asian Journal. 6: 2158-65. PMID 21671404 DOI: 10.1002/Asia.201100219 | 0.499 | |||
| 2011 | Shi L, Liu X, Zhang H, Jiang Y, Ma D. Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/heterocyclization process. The Journal of Organic Chemistry. 76: 4200-4. PMID 21495655 DOI: 10.1021/Jo200535E | 0.672 | |||
| 2011 | Wang Y, Zhu S, Ma D. Organocatalytic approach to polysubstituted piperidines and tetrahydropyrans. Organic Letters. 13: 1602-5. PMID 21361355 DOI: 10.1021/Ol200004S | 0.729 | |||
| 2011 | Ma D, Lu X, Shi L, Zhang H, Jiang Y, Liu X. Domino condensation/S-arylation/heterocyclization reactions: copper-catalyzed three-component synthesis of 2-N-substituted benzothiazoles. Angewandte Chemie (International Ed. in English). 50: 1118-21. PMID 21268208 DOI: 10.1002/Anie.201005787 | 0.693 | |||
| 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 | 0.838 | |||
| 2011 | Chen G, Xia H, Cai Y, Ma D, Yuan J, Yuan C. Synthesis and SAR study of diphenylbutylpiperidines as cell autophagy inducers. Bioorganic & Medicinal Chemistry Letters. 21: 234-9. PMID 21126871 DOI: 10.1016/J.Bmcl.2010.11.029 | 0.688 | |||
| 2011 | Han S, Pan H, Zhang J, Tan L, Ma D, Yuan J, Wu JR. Identification of a small molecule activator of novel PKCs for promoting glucose-dependent insulin secretion. Cell Research. 21: 588-99. PMID 20877311 DOI: 10.1038/Cr.2010.137 | 0.349 | |||
| 2011 | Chen G, Xia H, Cai Y, Ma D, Yuan J, Yuan C. Diphenylbutylpiperidine-based cell autophagy inducers: Design, synthesis and SAR studies Medchemcomm. 2: 315. DOI: 10.1039/C0Md00236D | 0.674 | |||
| 2011 | Jia J, Jiang C, Zhang X, Jiang Y, Ma D. CuI-catalyzed hydroxylation of aryl bromides under the assistance of 5-bromo-2-(1H-imidazol-2-yl)pyridine and related ligands Tetrahedron Letters. 52: 5593-5595. DOI: 10.1016/J.Tetlet.2011.08.059 | 0.621 | |||
| 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 | 0.767 | |||
| 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 | 0.808 | |||
| 2011 | Zuo Z, Ma D. Synthetic studies toward communesins Israel Journal of Chemistry. 51: 434-441. DOI: 10.1002/Ijch.201100014 | 0.705 | |||
| 2011 | Xu L, Jiang Y, Ma D. ChemInform Abstract: Synthesis of Tetrahydropyrrolo[1,2-a]quinoxalines and Tetrahydropyrido[1,2-a]quinoxalines via a One-Pot CuI-Catalyzed Aryl Amination-Hydrolysis-Condensation Process. Cheminform. 42: no-no. DOI: 10.1002/chin.201105168 | 0.656 | |||
| 2010 | Zuo Z, Xie W, Ma D. Total synthesis and absolute stereochemical assignment of (-)-communesin F. Journal of the American Chemical Society. 132: 13226-8. PMID 20812683 DOI: 10.1021/Ja106739G | 0.807 | |||
| 2010 | Ma A, Ma D. Enantioselective synthesis of polysubstituted cyclopentanones by organocatalytic double Michael addition reactions Organic Letters. 12: 3634-3637. PMID 20704408 DOI: 10.1021/Ol101414B | 0.453 | |||
| 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 | 0.761 | |||
| 2010 | Ben L, Jones ED, Zhou E, Li C, Baylis DC, Yu S, Wang M, He X, Coates JA, Rhodes DI, Pei G, Deadman JJ, Xie X, Ma D. Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 1: Tuning the N-substituents. Bioorganic & Medicinal Chemistry Letters. 20: 4012-4. PMID 20561788 DOI: 10.1016/J.Bmcl.2010.05.102 | 0.346 | |||
| 2010 | Zhou Q, Chen X, Ma D. Asymmetric, protecting-group-free total synthesis of (-)-englerin A. Angewandte Chemie (International Ed. in English). 49: 3513-6. PMID 20544902 DOI: 10.1002/Anie.201000888 | 0.712 | |||
| 2010 | Li W, Schlecker A, Ma D. Total synthesis of antimicrobial and antitumor cyclic depsipeptides. Chemical Communications (Cambridge, England). 46: 5403-20. PMID 20544117 DOI: 10.1039/C0Cc00629G | 0.403 | |||
| 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 | 0.793 | |||
| 2010 | Ma D, Geng Q, Zhang H, Jiang Y. Assembly of substituted phenothiazines by a sequentially controlled CuI/ L-proline-catalyzed cascade C-S and C-N bond formation. Angewandte Chemie (International Ed. in English). 49: 1291-4. PMID 20058286 DOI: 10.1002/Anie.200905646 | 0.589 | |||
| 2010 | Wang Y, Xu L, Ma D. Cu(I)/L-proline-catalyzed coupling of substituted 3-iodoprop-2-en-1-ols with 1-alkynes and subsequent cyclization: a convenient approach for synthesizing polysubstituted furans. Chemistry, An Asian Journal. 5: 74-6. PMID 20014002 DOI: 10.1002/Asia.200900523 | 0.404 | |||
| 2010 | Xia HG, Zhang L, Chen G, Zhang T, Liu J, Jin M, Ma X, Ma D, Yuan J. Control of basal autophagy by calpain1 mediated cleavage of ATG5. Autophagy. 6: 61-6. PMID 19901552 DOI: 10.4161/Auto.6.1.10326 | 0.624 | |||
| 2010 | Ma D, Zuo Z, Xie W. Synthesis of (-)-Communesin F Synfacts. 2011: 0006-0006. DOI: 10.1055/S-0030-1259130 | 0.625 | |||
| 2010 | Ma D, Xu L, Jiang Y. Synthesis of Tetrahydropyrrolo[1,2-a]quinoxalines and Tetrahydropyrido[1,2-a]quinoxalines via a One-Pot CuI-Catalyzed Aryl Amination-Hydrolysis-Condensation Process Synlett. 2010: 2285-2288. DOI: 10.1055/S-0030-1258030 | 0.664 | |||
| 2010 | Ma D, Zhou Q, Chen X. Synthesis of (-)-Englerin A Synfacts. 2010: 0972-0972. DOI: 10.1055/S-0030-1257934 | 0.739 | |||
| 2010 | Zhu S, Yu S, Wang Y, Ma D. Michael Addition of Aldehydes to 2-Amino-1-nitroethenes Synfacts. 2010: 943-943. DOI: 10.1055/S-0030-1257802 | 0.391 | |||
| 2010 | Jiang Y, Ma D, Maurer S, Liu W, Zhang X. An Efficient Synthesis of Phenol via CuI/8-Hydroxyquinoline-Catalyzed Hydroxylation of Aryl Halides and Potassium Hydroxide Synlett. 2010: 976-978. DOI: 10.1055/S-0029-1219548 | 0.678 | |||
| 2010 | Xu D, Zhang Y, Ma D. Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones Tetrahedron Letters. 51: 3827-3829. DOI: 10.1016/J.Tetlet.2010.05.077 | 0.419 | |||
| 2010 | Lu X, Shi L, Zhang H, Jiang Y, Ma D. Assembly of N-substituted pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones via copper catalyzed aryl amination Tetrahedron. 66: 5714-5718. DOI: 10.1016/J.Tet.2010.04.127 | 0.681 | |||
| 2010 | Hao C, Zhang Y, Jiang Y, Ma D. CuBr/N,N-Dimethylglycine-Catalyzed Coupling Reaction of 2-Chlorotrifluoroacetanilides with Phenols at Mild Conditions Chinese Journal of Chemistry. 28: 1645-1650. DOI: 10.1002/Cjoc.201090279 | 0.657 | |||
| 2010 | Pan Q, Ma D. Chiral Guanidine Catalyzed Annulation to the Core Structure of (‐)‐Huperzine A Chinese Journal of Chemistry. 21: 793-796. DOI: 10.1002/Cjoc.20030210716 | 0.463 | |||
| 2010 | Ding K, Zhang X, Ma D, Wang B. Synthesis and biological activity of l-aminoindan-l,3-dicarboxylic acid, a benzo-analogue of (1S, 3R)-ACPD Chinese Journal of Chemistry. 19: 1232-1238. DOI: 10.1002/Cjoc.20010191212 | 0.536 | |||
| 2010 | Ma D, Zhang Y, Zhang X, Wu S, Tao F. Synthesis of Benzofuran Analogue of Go6976, an Isoform-Selective Protein Kinase C Inhibitor Chinese Journal of Chemistry. 19: 488-492. DOI: 10.1002/Cjoc.20010190510 | 0.398 | |||
| 2010 | Ma D, Wu W, Qian J, Lang S, Ye Q. Synthesis of a Cyclic Analogue of Galardin Chinese Journal of Chemistry. 19: 286-290. DOI: 10.1002/CJOC.20010190315 | 0.35 | |||
| 2010 | Hao C, Zhang Y, Jiang Y, Ma D. ChemInform Abstract: CuBr/N,N-Dimethylglycine-Catalyzed Coupling Reaction of 2-Chlorotrifluoroacetanilides with Phenols at Mild Conditions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201104080 | 0.599 | |||
| 2010 | Lu X, Shi L, Zhang H, Jiang Y, Ma D. ChemInform Abstract: Assembly of N-Substituted Pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones via Copper Catalyzed Aryl Amination. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201048163 | 0.61 | |||
| 2010 | Maurer S, Liu W, Zhang X, Jiang Y, Ma D. ChemInform Abstract: An Efficient Synthesis of Phenol via CuI/8-Hydroxyquinoline-Catalyzed Hydroxylation of Aryl Halides and Potassium Hydroxide. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201030066 | 0.663 | |||
| 2010 | Wang H, Jiang Y, Gao K, Ma D. ChemInform Abstract: Facile Synthesis of 1,4-Benzodiazepin-3-ones from o-Bromobenzylamines and Amino Acids via Cascade Coupling/Condensation Process. Cheminform. 41. DOI: 10.1002/CHIN.201008182 | 0.588 | |||
| 2010 | Ma D, Xia C. ChemInform Abstract: CuI-Catalyzed Coupling Reaction of β-Amino Acids or Esters with Aryl Halides at Temperature Lower Than That Employed in the Normal Ullmann Reaction. Facile Synthesis of SB-214857. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200149064 | 0.38 | |||
| 2010 | Ding K, Ma D. ChemInform Abstract: Asymmetric Synthesis of α,α-Disubstituted Amino Acids by Diastereoselective Functionalization of Enantiopure Phenyloxazinones, Derivatives of Asymmetric Strecker Reaction Products of Aldehydes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200146193 | 0.336 | |||
| 2010 | Ma D, Xia C, Jiang J, Zhang J. ChemInform Abstract: First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200142235 | 0.613 | |||
| 2010 | Wang Y, Ma D. ChemInform Abstract: Synthesis of Enantiopure N-Protected 4,5-Disubstituted 3-Pyrrolidinones and N-Protected 2,5-Disubstituted 3-Pyrrolidinones via the Dieckmann Reaction of Dicarbonyl Compounds Derived from Enantiopure β-Amino Esters. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200135123 | 0.355 | |||
| 2010 | Ma D, Xia C, Tian H. ChemInform Abstract: Oxidation of Benzylic Methylene Compounds to Ketones with m-Chloroperoxybenzoic Acid and Oxygen. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200009060 | 0.739 | |||
| 2010 | Ma D, Tang G, Tian H, Zou G. ChemInform Abstract: Enantioselective Syntheses of α-Substituted Glutamic Acids and α,γ-Disubstituted Glutamic Acids by an Asymmetric Strecker Reaction. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199941180 | 0.672 | |||
| 2010 | Ma D, Cheng K. ChemInform Abstract: Enantioselective Synthesis of Functionalized α-Amino Acids via a Chiral Guanidine Catalyzed Michael Addition Reaction. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199935216 | 0.375 | |||
| 2010 | Ma D, Zhang Y, Yao J, Wu S, Tao F. ChemInform Abstract: Accelerating Effect Induced by the Structure of α-Amino Acid in the Copper-Catalyzed Coupling Reaction of Aryl Halides with α-Amino Acids. Synthesis of Benzolactam-V8. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199917212 | 0.327 | |||
| 2010 | Ma D, Zhang J. ChemInform Abstract: Enantioselective Syntheses of Tussilagine and Isotussilagine. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199909244 | 0.303 | |||
| 2010 | MA D, JIANG J. ChemInform Abstract: Pd/Cu-Catalyzed Couplings of β-Amino Esters with Aryl Bromides. Synthesis of Chiral 1,2,3,4-Tetrahydro-4-oxo-2-alkyl-1-quinolines. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199834171 | 0.32 | |||
| 2010 | MA D, TIAN H. ChemInform Abstract: Stereoselective Synthesis of (S)-MPPG, (S)-MTPG, and (S)-(+)-αM4CPG from (R)-4-Hydroxyphenylglycine. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199815205 | 0.638 | |||
| 2010 | MA D, TIAN H, SUN H, KOZIKOWSKI AP, PSHENICHKIN S, WROBLEWSKI JT. ChemInform Abstract: Synthesis and Biological Activity of Cyclic Analogues of MPPG and MCPG as Metabotropic Glutamate Receptor Antagonists. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199740239 | 0.643 | |||
| 2010 | MA D, YAO J. ChemInform Abstract: Synthesis of Chiral N-Aryl-α-amino Acids by Pd-Cu Catalyzed Couplings of Chiral α-Amino Acids with Aryl Halides Cheminform. 28: no-no. DOI: 10.1002/chin.199712198 | 0.317 | |||
| 2010 | LU X, JI J, MA D, SHEN W. ChemInform Abstract: Facile Synthesis of 1,4-Diketones via Palladium Complex-Catalyzed Isomerization of Alkynediols. Cheminform. 23: no-no. DOI: 10.1002/chin.199208139 | 0.33 | |||
| 2009 | Li W, Gan J, Ma D. Total synthesis of piperazimycin A: a cytotoxic cyclic hexadepsipeptide. Angewandte Chemie (International Ed. in English). 48: 8891-5. PMID 19839021 DOI: 10.1002/Anie.200904603 | 0.437 | |||
| 2009 | Jiang Y, Qin Y, Xie S, Zhang X, Dong J, Ma D. A general and efficient approach to aryl thiols: CuI-catalyzed coupling of aryl iodides with sulfur and subsequent reduction. Organic Letters. 11: 5250-3. PMID 19835369 DOI: 10.1021/Ol902186D | 0.689 | |||
| 2009 | Diao X, Wang Y, Jiang Y, Ma D. Assembly of substituted 1H-benzimidazoles and 1,3-dihydrobenzimidazol-2- ones via CuI/L-proline catalyzed coupling of aqueous ammonia with 2-iodoacetanilides and 2-iodophenylcarbamates Journal of Organic Chemistry. 74: 7974-7977. PMID 19775088 DOI: 10.1021/Jo9017183 | 0.659 | |||
| 2009 | Gan J, Ma D. Synthesis of 1,5-benzothiazepine dipeptide mimetics via two cul-catalyzed cross coupling reactions Organic Letters. 11: 2788-2790. PMID 19480438 DOI: 10.1021/Ol900943B | 0.491 | |||
| 2009 | Grauer A, Späth A, Ma D, König B. Metal-catalyzed derivatization of C(alpha)-tetrasubstituted amino acids and their use in the synthesis of cyclic peptides. Chemistry, An Asian Journal. 4: 1134-40. PMID 19472262 DOI: 10.1002/Asia.200900033 | 0.451 | |||
| 2009 | Jiang L, Lu X, Zhang H, Jiang Y, Ma D. CuI/4-hydro-L-proline as a more effective catalytic system for coupling of aryl bromides with N-boc hydrazine and aqueous ammonia. The Journal of Organic Chemistry. 74: 4542-6. PMID 19432437 DOI: 10.1021/Jo9006738 | 0.67 | |||
| 2009 | Ma D, Xie S, Xue P, Zhang X, Dong J, Jiang Y. Efficient and economical access to substituted benzothiazoles: copper-catalyzed coupling of 2-haloanilides with metal sulfides and subsequent condensation. Angewandte Chemie (International Ed. in English). 48: 4222-5. PMID 19425042 DOI: 10.1002/Anie.200900486 | 0.626 | |||
| 2009 | Li L, Wang M, Zhang X, Jiang Y, Ma D. Assembly of substituted 3-methyleneisoindolin-1-ones via a CuI/l-proline-catalyzed domino reaction process of 2-bromobenzamides and terminal alkynes. Organic Letters. 11: 1309-12. PMID 19226134 DOI: 10.1021/Ol9000922 | 0.672 | |||
| 2009 | Sun W, Nikolovska-Coleska Z, Qin D, Sun H, Yang CY, Bai L, Qiu S, Wang Y, Ma D, Wang S. Design, synthesis, and evaluation of potent, nonpeptidic mimetics of second mitochondria-derived activator of caspases. Journal of Medicinal Chemistry. 52: 593-6. PMID 19138149 DOI: 10.1021/Jm801101Z | 0.512 | |||
| 2009 | Ma D, Wang H, Gao K, Jiang Y. Assembly of Substituted Homophthalimides via CuI-Catalyzed Coupling of 2-Bromobenzamides with β-Keto Ester Heterocycles. 79: 695. DOI: 10.3987/com-08-s(d)36 | 0.591 | |||
| 2009 | Cai Q, Zhang H, Zou B, Xie X, Zhu W, He G, Wang J, Pan X, Chen Y, Yuan Q, Liu F, Lu B, Ma D. Amino acid-promoted Ullmann-type coupling reactions and their applications in organic synthesis Pure and Applied Chemistry. 81: 227-234. DOI: 10.1351/Pac-Con-08-08-19 | 0.835 | |||
| 2009 | Jiang Z, Yao H, Zhang Z, Yang C, Liu Z, Tao Y, Qin J, Ma D. Synthesis of ortho-Linked Oligo-9,9′-spirobifluorenes Synfacts. 2009: 977-977. DOI: 10.1055/S-0029-1217673 | 0.443 | |||
| 2009 | Li L, Wang M, Zhang X, Jiang Y, Ma D. Synthesis of Isoindolin-1-ones via Copper-Catalyzed IntramolecularCyclization Synfacts. 2009: 605-605. DOI: 10.1055/S-0029-1216698 | 0.554 | |||
| 2009 | Wu Y, Zhang Y, Jiang Y, Ma D. Synthesis of polysubstituted 1,2-dihydroisoquinolines via a CuI-catalyzed arylation/condensation cascade process Tetrahedron Letters. 50: 3683-3685. DOI: 10.1016/J.Tetlet.2009.03.159 | 0.652 | |||
| 2009 | Wang H, Jiang Y, Gao K, Ma D. Facile synthesis of 1,4-benzodiazepin-3-ones from o-bromobenzylamines and amino acids via a cascade coupling/condensation process Tetrahedron. 65: 8956-8960. DOI: 10.1016/J.Tet.2009.06.104 | 0.642 | |||
| 2009 | Wang L, Zhang X, Jiang Y, Ma D. An efficient synthesis of isocoumarins via a CuI catalyzed cascade reaction process Science in China Series B: Chemistry. 52: 1616-1621. DOI: 10.1007/S11426-009-0197-6 | 0.696 | |||
| 2009 | Wu Y, Zhang Y, Jiang Y, Ma D. ChemInform Abstract: Synthesis of Polysubstituted 1,2-Dihydroisoquinolines via a CuI-Catalyzed Arylation/Condensation Cascade Process. Cheminform. 40. DOI: 10.1002/CHIN.200941153 | 0.641 | |||
| 2009 | Wang H, Gao K, Jiang Y, Ma D. ChemInform Abstract: Assembly of Substituted Homophthalimides via CuI-Catalyzed Coupling of 2-Bromobenzamides with β-Keto Ester. Cheminform. 40. DOI: 10.1002/CHIN.200941151 | 0.595 | |||
| 2009 | Zhu S, Wang Y, Ma D. Enantioselective Organocatalytic Conjugate Addition of Aldehydes to α,β-Unsaturated Thiol Esters Advanced Synthesis & Catalysis. 351: 2563-2566. DOI: 10.1002/Adsc.200900449 | 0.727 | |||
| 2008 | Wang J, Ma A, Ma D. Organocatalytic Michael addition of aldehydes to γ-keto-α, β-unsaturated esters. an efficient entry to versatile chiral building blocks Organic Letters. 10: 5425-5428. PMID 19006393 DOI: 10.1021/Ol802354U | 0.417 | |||
| 2008 | Ma D, Cai Q. Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles Accounts of Chemical Research. 41: 1450-1460. PMID 18698852 DOI: 10.1021/Ar8000298 | 0.634 | |||
| 2008 | Wang Y, Zhang F, Zhang Y, Liu JO, Ma D. Synthesis and antitumor activity of cyclodepsipeptide zygosporamide and its analogues. Bioorganic & Medicinal Chemistry Letters. 18: 4385-7. PMID 18606540 DOI: 10.1016/J.Bmcl.2008.06.066 | 0.322 | |||
| 2008 | Yuan Q, Ma D. A one-pot coupling/hydrolysis/condensation process to pyrrolo[1,2-a]quinoxaline. The Journal of Organic Chemistry. 73: 5159-62. PMID 18522423 DOI: 10.1021/Jo8008098 | 0.417 | |||
| 2008 | Wang B, Lu B, Jiang Y, Zhang Y, Ma D. Assembly of isoquinolines via CuI-catalyzed coupling of beta-keto esters and 2-halobenzylamines. Organic Letters. 10: 2761-3. PMID 18507393 DOI: 10.1021/Ol800900A | 0.616 | |||
| 2008 | Wang J, Yu F, Zhang X, Ma D. Enantioselective assembly of substituted dihydropyrones via organocatalytic reaction in water media. Organic Letters. 10: 2561-4. PMID 18476713 DOI: 10.1021/Ol800835M | 0.531 | |||
| 2008 | Tan L, Ma D. Total synthesis of salinamide A: a potent anti-inflammatory bicyclic depsipeptide. Angewandte Chemie (International Ed. in English). 47: 3614-7. PMID 18383490 DOI: 10.1002/Anie.200800397 | 0.438 | |||
| 2008 | Xie W, Ding D, Zi W, Li G, Ma D. Total synthesis and structure assignment of papuamide B, a potent marine cyclodepsipeptide with anti-HIV properties. Angewandte Chemie (International Ed. in English). 47: 2844-8. PMID 18318032 DOI: 10.1002/Anie.200705557 | 0.771 | |||
| 2008 | Chen Y, Wang Y, Sun Z, Ma D. Elaboration of 2-(trifluoromethyl)indoles via a cascade coupling/condensation/deacylation process. Organic Letters. 10: 625-8. PMID 18193883 DOI: 10.1021/Ol7029382 | 0.436 | |||
| 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 | 0.77 | |||
| 2008 | Guo L, Li B, Huang W, Pei G, Ma D. Elaboration of the OxazepineRing System via CuI/l-Proline-Catalyzed IntramolecularAryl Amination Synlett. 2008: 1833-1836. DOI: 10.1055/S-2008-1078506 | 0.435 | |||
| 2008 | Tan L, Ma D. Synthesis of Salinamide A Synfacts. 2008: 902-902. DOI: 10.1055/S-2008-1077996 | 0.551 | |||
| 2008 | Chen Y, Xie X, Ma D. Cascade Process from Anilines to Indoles Involving a Copper-Catalyzed Arylation Synfacts. 2008: 133-133. DOI: 10.1055/S-2007-992464 | 0.379 | |||
| 2008 | Ma A, Zhu S, Ma D. Enantioselective organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in water Tetrahedron Letters. 49: 3075-3077. DOI: 10.1016/J.Tetlet.2008.03.051 | 0.702 | |||
| 2008 | Wang B, Lu B, Jiang Y, Zhang Y, Ma D. ChemInform Abstract: Assembly of Isoquinolines via CuI-Catalyzed Coupling of β-Keto Esters and 2-Halobenzylamines. Cheminform. 39. DOI: 10.1002/CHIN.200845159 | 0.575 | |||
| 2007 | Chen Y, Xie X, Ma D. Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation-condensation process. The Journal of Organic Chemistry. 72: 9329-34. PMID 17975934 DOI: 10.1021/Jo702059Q | 0.426 | |||
| 2007 | Zou B, Yuan Q, Ma D. Cascade coupling/cyclization process to N-substituted 1,3-dihydrobenzimidazol-2-ones. Organic Letters. 9: 4291-4. PMID 17867696 DOI: 10.1021/Ol701792J | 0.503 | |||
| 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 | 0.833 | |||
| 2007 | Lu B, Wang B, Zhang Y, Ma D. CuI-catalyzed domino process to 2,3-disubstituted benzofurans from 1-bromo-2-iodobenzenes and beta-keto esters. The Journal of Organic Chemistry. 72: 5337-41. PMID 17579459 DOI: 10.1021/Jo070729R | 0.347 | |||
| 2007 | Liu F, Ma D. Assembly of conjugated enynes and substituted indoles via CuI/amino acid-catalyzed coupling of 1-alkynes with vinyl iodides and 2-bromotrifluoroacetanilides. The Journal of Organic Chemistry. 72: 4844-50. PMID 17530901 DOI: 10.1021/Jo070547X | 0.563 | |||
| 2007 | Zou B, Yuan Q, Ma D. Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process. Angewandte Chemie (International Ed. in English). 46: 2598-601. PMID 17348051 DOI: 10.1002/Anie.200700071 | 0.407 | |||
| 2007 | He G, Wang J, Ma D. Highly convergent route to cyclopeptide alkaloids: total synthesis of ziziphine N. Organic Letters. 9: 1367-9. PMID 17346058 DOI: 10.1021/Ol070271F | 0.632 | |||
| 2007 | Ma D, Yu S, Li B, Chen L, Chen R, Yu K, Zhang L, Chen Z, Zhong D, Gong Z, Wang R, Jiang H, Pei G. Synthesis and biological evaluation of 1,3,3,4-tetrasubstituted pyrrolidine CCR5 receptor antagonists. Discovery of a potent and orally bioavailable anti-HIV agent. Chemmedchem. 2: 187-93. PMID 17163560 DOI: 10.1002/Cmdc.200600182 | 0.354 | |||
| 2007 | Zhang H, Cao W, Ma D. L‐Proline‐Promoted CuI‐Catalyzed C‐S Bond Formation between Aryl Iodides and Thiols Synthetic Communications. 37: 25-35. DOI: 10.1080/00397910600977533 | 0.404 | |||
| 2007 | Sun Z, Yu S, Ding Z, Ma D. Copper-Catalyzed Asymmetric Synthesis of Dihydropyridines Synfacts. 2007: 1025-1025. DOI: 10.1055/S-2007-968980 | 0.443 | |||
| 2007 | Zou B, Yuan Q, Ma D. Cu-Catalyzed One-Pot Synthesis of 1,2-Disubstituted Benzimidazoles Synfacts. 2007: 644-644. DOI: 10.1055/S-2007-968543 | 0.367 | |||
| 2007 | Ma D, Xie X, Chen Y. Copper-Catalyzed Enantioselective Arylation of 2-Methylacetoacetates Synfacts. 2007: 0289-0289. DOI: 10.1055/S-2007-968265 | 0.406 | |||
| 2007 | Zhang H, Ma D, Cao W. N,N-Dimethylglycine-Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Aliphatic Alcohols. Cheminform. 38. DOI: 10.1055/S-2007-968010 | 0.406 | |||
| 2007 | Wang J, Schaeffler L, He G, Ma D. Total synthesis and stereochemistry assignment of 15-membered peptide alkaloids abyssenine B and mucronine E Tetrahedron Letters. 48: 6717-6721. DOI: 10.1016/J.Tetlet.2007.07.142 | 0.587 | |||
| 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 | 0.549 | |||
| 2006 | Xie X, Chen Y, Ma D. Enantioselective arylation of 2-methylacetoacetates catalyzed by CuI/trans-4-hydroxy-L-proline at low reaction temperatures. Journal of the American Chemical Society. 128: 16050-1. PMID 17165754 DOI: 10.1021/Ja066991J | 0.448 | |||
| 2006 | Wu Q, Ma D. Recent progress on the total synthesis of natural products in China. Natural Product Reports. 23: 772-88. PMID 17003909 DOI: 10.1039/B609469B | 0.374 | |||
| 2006 | Pu X, Ma D. Facile entry to substituted decahydroquinoline alkaloids. Total synthesis of lepadins A-E and H Journal of Organic Chemistry. 71: 6562-6572. PMID 16901144 DOI: 10.1021/Jo061070C | 0.422 | |||
| 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 | 0.806 | |||
| 2006 | Yu S, Pu X, Cheng T, Wang R, Ma D. Total synthesis of clavepictines A and B and pictamine. Organic Letters. 8: 3179-82. PMID 16836360 DOI: 10.1021/Ol060960B | 0.405 | |||
| 2006 | Ma D, Zou B, Cai G, Hu X, Liu JO. Total synthesis of the cyclodepsipeptide apratoxin A and its analogues and assessment of their biological activities. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 7615-26. PMID 16832801 DOI: 10.1002/Chem.200600599 | 0.426 | |||
| 2006 | Cai Q, He G, Ma D. Mild and nonracemizing conditions for Ullmann-type diaryl ether formation between aryl iodides and tyrosine derivatives. The Journal of Organic Chemistry. 71: 5268-73. PMID 16808515 DOI: 10.1021/Jo0606960 | 0.677 | |||
| 2006 | Cai Q, Zou B, Ma D. Mild Ullmann-type biaryl ether formation reaction by combination of ortho-substituent and ligand effects. Angewandte Chemie (International Ed. in English). 45: 1276-9. PMID 16425327 DOI: 10.1002/Anie.200503538 | 0.551 | |||
| 2006 | Ma D, Jiang Y, Chen F, Gong LK, Ding K, Xu Y, Wang R, Ge A, Ren J, Li J, Li J, Ye Q. Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids. Journal of Medicinal Chemistry. 49: 456-8. PMID 16420030 DOI: 10.1021/Jm051101G | 0.638 | |||
| 2006 | Zhu W, Ma D. Formation of arylboronates by a CuI-catalyzed coupling reaction of pinacolborane with aryl iodides at room temperature. Organic Letters. 8: 261-3. PMID 16408890 DOI: 10.1021/Ol052633U | 0.434 | |||
| 2006 | Ma D, Zhu W. Efficient Entry to Polysubstituted Pyrrolizidines, Indolizidines and Quinolizidines via a Sequential Reaction Process Synlett. 2006: 1181-1184. DOI: 10.1055/S-2006-932488 | 0.402 | |||
| 2006 | He G, Wang J, Ma D. This Paper Has Been Withdrawn.Highly Convergent Route to Cyclopeptide Alkaloids. Total Synthesis of Ziziphine N Organic Letters. 0-0. DOI: 10.1021/Ol062639Z | 0.563 | |||
| 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 | 0.65 | |||
| 2006 | Cai G, Zhu W, Ma D. A sequential reaction process to assemble polysubstituted indolizidines, quinolizidines and quinolizidine analogues Tetrahedron. 62: 5697-5708. DOI: 10.1016/J.Tet.2006.03.068 | 0.401 | |||
| 2006 | Lu B, Xie X, Zhu J, Ma D. Sodium Amalgam, a Useful Reducing Reagent for Formation of Amines from Azides Bearing a Variety of Functional Groups. Cheminform. 37. DOI: 10.1002/Cjoc.200591637 | 0.717 | |||
| 2006 | Ma D, Zhu J, Yu S, Pan X. Synthetic Studies Toward Two Marine Cyclic Peptides Cheminform. 37. DOI: 10.1002/chin.200622262 | 0.755 | |||
| 2005 | Zhu W, Cai G, Ma D. A formal [3+2] cycloaddition process with nonactivated aziridines to polysubstituted indolizidines. Organic Letters. 7: 5545-8. PMID 16320987 DOI: 10.1021/Ol0513692 | 0.39 | |||
| 2005 | Xie X, Cai G, Ma D. CuI/L-proline-catalyzed coupling reactions of aryl halides with activated methylene compounds. Organic Letters. 7: 4693-5. PMID 16209512 DOI: 10.1021/Ol0518838 | 0.463 | |||
| 2005 | Zou B, Long K, Ma D. Total synthesis and cytotoxicity studies of a cyclic depsipeptide with proposed structure of palau'amide. Organic Letters. 7: 4237-40. PMID 16146396 DOI: 10.1021/Ol051685G | 0.374 | |||
| 2005 | Yang H, Xie W, Xue X, Yang K, Ma J, Liang W, Zhao Q, Zhou Z, Pei D, Ziebuhr J, Hilgenfeld R, Yuen KY, Wong L, Gao G, Chen S, ... ... Ma D, et al. Design of wide-spectrum inhibitors targeting coronavirus main proteases. Plos Biology. 3: e324. PMID 16128623 DOI: 10.1371/Journal.Pbio.0030324 | 0.637 | |||
| 2005 | Yu S, Zhu W, Ma D. A one-pot formal [4 + 2] cycloaddition approach to substituted piperidines, indolizidines, and quinolizidines. total synthesis of indolizidine (-)-209I. The Journal of Organic Chemistry. 70: 7364-70. PMID 16122260 DOI: 10.1021/Jo051080Y | 0.481 | |||
| 2005 | Zhang H, Cai Q, Ma D. Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles. The Journal of Organic Chemistry. 70: 5164-73. PMID 15960520 DOI: 10.1021/Jo0504464 | 0.619 | |||
| 2005 | Xie W, Zou B, Pei D, Ma D. Total synthesis of cyclic tetrapeptide FR235222, a potent immunosuppressant that inhibits mammalian histone deacetylases. Organic Letters. 7: 2775-7. PMID 15957944 DOI: 10.1021/Ol050991R | 0.707 | |||
| 2005 | Zhu W, Ma D. Synthesis of aryl sulfones via L-proline-promoted CuI-catalyzed coupling reaction of aryl halides with sulfinic acid salts. The Journal of Organic Chemistry. 70: 2696-700. PMID 15787561 DOI: 10.1021/Jo047758B | 0.496 | |||
| 2005 | Zhu W, Dong D, Pu X, Ma D. An efficient sequential reaction process to polysubstituted indolizidines and quinolizidines and its application to the total synthesis of indolizidine 223A. Organic Letters. 7: 705-8. PMID 15704930 DOI: 10.1021/Ol047476Y | 0.437 | |||
| 2005 | Yang H, Xie W, Xue X, Yang K, Ma J, Liang W, Zhao Q, Zhou Z, Pei D, Ziebuhr J, Hilgenfeld R, Yuen KY, Wong L, Gao G, Chen S, ... ... Ma D, et al. Correction: Design of Wide-Spectrum Inhibitors Targeting Coronavirus Main Proteases Plos Biology. 3: e428. DOI: 10.1371/Journal.Pbio.0030428 | 0.615 | |||
| 2005 | Ma D, Cai Q, Xie X. CuI/N,N-Dimethylglycine-Catalyzed Cross-Coupling Reaction of Vinyl Halides with Phenols and Its Application to the Assembly of Substituted Benzofurans. Cheminform. 36. DOI: 10.1055/S-2005-871543 | 0.615 | |||
| 2005 | Cai Q, Zhu W, Zhang H, Zhang Y, Ma D. Preparation of N-Aryl Compounds by Amino Acid-Promoted Ullmann-Type Coupling Reactions. Cheminform. 36. DOI: 10.1055/S-2004-831196 | 0.591 | |||
| 2005 | Ma D, Cai Q, Zhu W, Zhang H, Zhang Y. Preparation ofN-Aryl Compounds by Amino Acid-Promoted Ullmann-Type Coupling Reactions Synthesis. 2005: 496-499. DOI: 10.1055/S-2004-831196 | 0.536 | |||
| 2004 | Ma D, Xie W, Zou B, Lei Q, Pei D. An efficient and tunable route to AG7088, a rhinovirus protease inhibitor. Tetrahedron Letters. 45: 8103-8105. PMID 32287436 DOI: 10.1016/J.Tetlet.2004.08.179 | 0.734 | |||
| 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 | 0.815 | |||
| 2004 | Ma D, Liu F. CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine. Chemical Communications (Cambridge, England). 1934-5. PMID 15340608 DOI: 10.1039/B407090A | 0.534 | |||
| 2004 | Pu X, Ma D. Total synthesis of lepadins B, D, E, and H; determination of the configuration of the latter three alkaloids Angewandte Chemie - International Edition. 43: 4222-4225. PMID 15307093 DOI: 10.1002/Anie.200460128 | 0.305 | |||
| 2004 | Pan X, Cai Q, Ma D. CuI/N,N-dimethylglycine-catalyzed coupling of vinyl halides with amides or carbamates. Organic Letters. 6: 1809-12. PMID 15151420 DOI: 10.1021/Ol049464I | 0.782 | |||
| 2004 | Zhu W, Ma D. Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions. Chemical Communications (Cambridge, England). 888-9. PMID 15045114 DOI: 10.1039/B400878B | 0.486 | |||
| 2004 | Pan Q, Zou B, Wang Y, Ma D. Diastereoselective aldol reaction of N,N-dibenzyl-alpha-amino aldehydes with ketones catalyzed by proline. Organic Letters. 6: 1009-12. PMID 15012087 DOI: 10.1021/Ol049927K | 0.415 | |||
| 2004 | Ma D, Cai Q. L-Proline Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Indoles, Pyrroles, Imidazoles or Pyrazoles. Cheminform. 35. DOI: 10.1055/S-2003-44995 | 0.578 | |||
| 2004 | Tang G, Tian H, Ma D. Asymmetric Strecker reaction of γ-keto acids. Facile entry to α-substituted and α,γ-disubstituted glutamic acids Tetrahedron. 60: 10547-10552. DOI: 10.1016/J.Tet.2004.07.100 | 0.696 | |||
| 2004 | Ma D, Zhu W. Stereospecific Total Synthesis of (-)-8-epi-Hyperaspine (I). Cheminform. 35. DOI: 10.1002/CHIN.200410188 | 0.33 | |||
| 2004 | Zou B, Wei J, Cai G, Ma D. Synthesis of an Oxazoline Analogue (Ia) of Apratoxin A (Ib). Cheminform. 35. DOI: 10.1002/CHIN.200405156 | 0.34 | |||
| 2003 | Zhu J, Ma D. Total synthesis of microsclerodermin E. Angewandte Chemie (International Ed. in English). 42: 5348-51. PMID 14613173 DOI: 10.1002/Anie.200352423 | 0.721 | |||
| 2003 | Ma D, Cai Q. N,N-Dimethyl Glycine-Promoted Ullmann Coupling Reaction of Phenols and Aryl Halides Organic Letters. 5: 3799-3802. PMID 14535713 DOI: 10.1021/Ol0350947 | 0.579 | |||
| 2003 | Zou B, Wei J, Cai G, Ma D. Synthesis of an oxazoline analogue of apratoxin A. Organic Letters. 5: 3503-6. PMID 12967310 DOI: 10.1021/Ol035332Y | 0.392 | |||
| 2003 | Ma D, Cai Q, Zhang H. Mild method for Ullmann coupling reaction of amines and aryl halides. Organic Letters. 5: 2453-5. PMID 12841753 DOI: 10.1021/Ol0346584 | 0.599 | |||
| 2003 | Pu X, Ma D. Asymmetric total synthesis of (-)-alkaloid 223A and its 6-epimer Journal of Organic Chemistry. 68: 4400-4405. PMID 12762743 DOI: 10.1021/Jo0341261 | 0.39 | |||
| 2003 | Ma D, Xia C, Jiang J, Zhang J, Tang W. Aromatic nucleophilic substitution or CuI-catalyzed coupling route to martinellic acid. The Journal of Organic Chemistry. 68: 442-51. PMID 12530870 DOI: 10.1021/Jo026125Z | 0.782 | |||
| 2003 | Ma N, Ma D. Asymmetric synthesis of (-)-deoxoprosophylline Tetrahedron Asymmetry. 14: 1403-1406. DOI: 10.1016/S0957-4166(03)00275-1 | 0.364 | |||
| 2003 | Ma D, Ma N. Stereospecific Route to Enantiopure All cis-2,3,6-Trisubstituted Piperidines. Facile Synthesis of (-)-Deoxocassine and (+)-Azimic Acid. Cheminform. 34. DOI: 10.1016/S0040-4039(03)00820-7 | 0.437 | |||
| 2003 | Ma D, Zhu W. Stereospecific total synthesis of (−)-8-epi-hyperaspine Tetrahedron Letters. 44: 8609-8612. DOI: 10.1016/J.Tetlet.2003.09.149 | 0.406 | |||
| 2003 | Xia C, Heng L, Ma D. Total Synthesis of (.+-.)-Martinelline. Cheminform. 34. DOI: 10.1002/CHIN.200312187 | 0.657 | |||
| 2002 | Ma D, Tang G, Kozikowski AP. Synthesis of 7-substituted benzolactam-V8s and their selectivity for protein kinase C isozymes Organic Letters. 4: 2377-2380. PMID 12098251 DOI: 10.1021/Ol026125L | 0.609 | |||
| 2002 | Rong SB, Enyedy IJ, Qiao L, Zhao L, Ma D, Pearce LL, Lorenzo PS, Stone JC, Blumberg PM, Wang S, Kozikowski AP. Structural basis of RasGRP binding to high-affinity PKC ligands. Journal of Medicinal Chemistry. 45: 853-60. PMID 11831896 DOI: 10.1021/Jm010422Z | 0.465 | |||
| 2002 | Ma D, Zhu W. Two-component method to enantiopure quinolizidinones and Indolizidinones. Total synthesis of (-)-lasubine II. Organic Letters. 3: 3927-9. PMID 11720571 DOI: 10.1021/Ol016802W | 0.445 | |||
| 2002 | Ma D, Pu X, Wang J. Efficient formal synthesis of the dendrobatid alkaloid, indolizidine (-)-209B Tetrahedron Asymmetry. 13: 2257-2260. DOI: 10.1016/S0957-4166(02)00577-3 | 0.366 | |||
| 2002 | Jiang Y, Ma D. Synthesis of enantiopure substituted dihydrofurans via the reaction of (S)-glyceraldehyde acetonide- or Garner aldehyde acetonide-derived enones with sulfonium ylides Tetrahedron: Asymmetry. 13: 1033-1038. DOI: 10.1016/S0957-4166(02)00239-2 | 0.673 | |||
| 2002 | Ma D, Ding K, Tian H, Wang B, Cheng D. Asymmetric synthesis of (S)-1-aminoindan-1,5-dicarboxylic acid and related analogues via intramolecular acylation of enantiopure α,α-disubstituted amino acids Tetrahedron: Asymmetry. 13: 961-969. DOI: 10.1016/S0957-4166(02)00224-0 | 0.765 | |||
| 2002 | Ma D, Pan Q, Han F. Diastereoselective Henry reactions of N,N-dibenzyl α-amino aldehydes with nitromethane catalyzed by enantiopure guanidines Tetrahedron Letters. 43: 9401-9403. DOI: 10.1016/S0040-4039(02)02332-8 | 0.445 | |||
| 2002 | Xia C, Heng L, Ma D. Total synthesis of (±)-martinelline Tetrahedron Letters. 43: 9405-9409. DOI: 10.1016/S0040-4039(02)02331-6 | 0.691 | |||
| 2002 | Ma D, Zou B, Zhu W, Xu H. A short synthesis of the HIV-protease inhibitor nelfinavir via a diastereoselective addition of ammonia to the α,β-unsaturated sulfoxide derived from (R)-glyceraldehyde acetonide Tetrahedron Letters. 43: 8511-8513. DOI: 10.1016/S0040-4039(02)02077-4 | 0.41 | |||
| 2002 | Jiang Y, Ma D. Regioselective acylation at the 5- or 6-position of l-tryptophan derivatives Tetrahedron Letters. 43: 7013-7015. DOI: 10.1016/S0040-4039(02)01580-0 | 0.651 | |||
| 2001 | Ma D, Xia C. CuI-catalyzed coupling reaction of β-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857 Organic Letters. 3: 2583-2586. PMID 11483066 DOI: 10.1021/Ol016258R | 0.702 | |||
| 2001 | Ma D, Xia C, Jiang J, Zhang J. First total synthesis of martinellic acid, a naturally occurring bradykinin receptor antagonist. Organic Letters. 3: 2189-91. PMID 11440576 DOI: 10.1021/Ol016043H | 0.704 | |||
| 2001 | Ma D, Zhang T, Wang G, Kozikowski AP, Lewin NE, Blumberg PM. Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C. Bioorganic & Medicinal Chemistry Letters. 11: 99-101. PMID 11206480 DOI: 10.1016/S0960-894X(00)00609-0 | 0.36 | |||
| 2001 | Wang Y, Ma D. Synthesis of enantiopure N-protected 4,5-disubstituted 3-pyrrolidinones and N-protected 2,5-disubstituted 3-pyrrolidinones via the Dieckmann reaction of dicarbonyl compounds derived from enantiopure β-amino esters Tetrahedron: Asymmetry. 12: 725-730. DOI: 10.1016/S0957-4166(01)00115-X | 0.464 | |||
| 2001 | Ma D, Wu W, Deng P. Facile synthesis of (+)-α-allokainic acid via Pd-catalyzed hydrogenolysis of allyl acetate derived from trans-4-hydroxy-L-proline Tetrahedron Letters. 42: 6929-6931. DOI: 10.1016/S0040-4039(01)01440-X | 0.383 | |||
| 2001 | Ma D, Wu Q. Synthesis of the biaryl moiety of the proteasome inhibitors TMC-95 via a ligandless Pd(OAc)2-catalyzed Suzuki-coupling reaction Tetrahedron Letters. 42: 5279-5281. DOI: 10.1016/S0040-4039(01)00966-2 | 0.425 | |||
| 2001 | Ding K, Ma D. Asymmetric synthesis of α,α-disubstituted amino acids by diastereoselective functionalization of enantiopure phenyloxazinones, derivatives of asymmetric Strecker reaction products of aldehydes Tetrahedron. 57: 6361-6366. DOI: 10.1016/S0040-4020(01)00502-6 | 0.6 | |||
| 2001 | Ma D, Cao Y, Wu W, Jiang Y. ChemInform Abstract: Synthesis of (2S,1′R,2′R,3′R)-2-(2′,3′-Dicarboxycyclopropyl)glycine via the Stereochemically Controlled Cyclopropanation of (S)-Glyceraldehyde Acetonide-Derived Enones. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200102188 | 0.58 | |||
| 2000 | Ma D, Sun H. General route to 2,4,5-trisubstituted piperidines from enantiopure beta-amino esters. Total synthesis of pseudodistomin B triacetate and pseudodistomin F. The Journal of Organic Chemistry. 65: 6009-16. PMID 10987934 DOI: 10.1021/Jo000447Q | 0.413 | |||
| 2000 | Ma D, Sun H. A simple and stereospecfic route to 2,6-disubstituted 4-hydroxypiperidines. Synthesis of dendrobate alkaloid (+)-241D and formal synthesis of (-)-indolizidine 167B. Organic Letters. 2: 2503-5. PMID 10956532 DOI: 10.1021/Ol006176N | 0.583 | |||
| 2000 | Ma D, Jiang Y. Stereocontrolled cyclopropanation of Garner's aldehyde derived enones Tetrahedron: Asymmetry. 11: 3727-3736. DOI: 10.1016/S0957-4166(00)00327-X | 0.369 | |||
| 2000 | Ma D, Wu Q. Enantioselective construction of the oxidized tryptophan fragment of proteasome inhibitors TMC-95A and TMC-95B Tetrahedron Letters. 41: 9089-9093. DOI: 10.1016/S0040-4039(00)01657-9 | 0.368 | |||
| 2000 | Ma D, Sun H. Total synthesis of (2S,3S,4R)-plakoridine A Tetrahedron Letters. 41: 1947-1950. DOI: 10.1016/S0040-4039(00)00096-4 | 0.607 | |||
| 2000 | Ma D, Cao Y, Wu W, Jiang Y. Synthesis of (2S,1′R,2′R,3′R)-2-(2′,3′-Dicarboxycyclopropyl)-glycine via the Stereochemically Controlled Cyclopropanation of (S)-Glyceraldehyde Acetonide-Derived Enones Tetrahedron. 56: 7447-7456. DOI: 10.1016/S0040-4020(00)00677-3 | 0.442 | |||
| 2000 | Ma D, Ding K. ChemInform Abstract: Synthesis of Enantiopure α,α-Disubstituted Amino Acids from the Asymmetric Strecker Reaction Products of Aldehydes. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200045199 | 0.308 | |||
| 1999 | Ma D, Tian H, Zou G. Asymmetric Strecker-Type Reaction of alpha-Aryl Ketones. Synthesis of (S)-alphaM4CPG, (S)-MPPG, (S)-AIDA, and (S)-APICA, the Antagonists of Metabotropic Glutamate Receptors. The Journal of Organic Chemistry. 64: 120-125. PMID 11674092 DOI: 10.1021/Jo981297A | 0.687 | |||
| 1999 | Ibarreta D, Duchén M, Ma D, Qiao L, Kozikowski AP, Etcheberrigaray R. Benzolactam (BL) enhances sAPP secretion in fibroblasts and in PC12 cells. Neuroreport. 10: 1035-40. PMID 10321481 DOI: 10.1097/00001756-199904060-00026 | 0.433 | |||
| 1999 | Ma D, Zhang J. β-Amino ester route to tussilagine, isotussilagine and (–)-petasinecine Journal of the Chemical Society-Perkin Transactions 1. 1703-1708. DOI: 10.1039/A901330J | 0.41 | |||
| 1999 | Ma D, Tang W, Kozikowski AP, Lewin NE, Blumberg PM. General and Stereospecific Route to 9-Substituted, 8,9-Disubstituted, and 9,10-Disubstituted Analogues of Benzolactam-V8 The Journal of Organic Chemistry. 64: 6366-6373. DOI: 10.1021/Jo990605H | 0.619 | |||
| 1999 | Ma D, Tian H, Zou G. Asymmetric strecker-type reaction of α-aryl ketones. Synthesis of (S)- αM4CPG, (S)-MPPG, (S)-AIDA, and (S)-APICA, the antagonists of metabotropic glutamate receptors Journal of Organic Chemistry. 64: 120-125. DOI: 10.1021/jo981297a | 0.671 | |||
| 1999 | Ma D, Cheng K. Enantioselective synthesis of functionalized α-amino acids via a chiral guanidine catalyzed Michael addition reaction Tetrahedron: Asymmetry. 10: 713-719. DOI: 10.1016/S0957-4166(99)00038-5 | 0.467 | |||
| 1999 | Ma D, Xia C, Tian H. Oxidation of benzylic methylene compounds to ketones with m-chloroperoxybenzoic acid and oxygen Tetrahedron Letters. 40: 8915-8917. DOI: 10.1016/S0040-4039(99)01886-9 | 0.767 | |||
| 1999 | Ma D, Tang G, Tian H, Zou G. Enantioselective syntheses of α-substituted glutamic acids and α,γ-disubstituted glutamic acids by an asymmetric Strecker reaction Tetrahedron Letters. 40: 5753-5756. DOI: 10.1016/S0040-4039(99)01121-1 | 0.711 | |||
| 1999 | Ma D, Sun H. Diastereoselective synthesis of 2,4,5-trisubstituted piperidines from enantiopure β-amino esters Tetrahedron Letters. 40: 3609-3612. DOI: 10.1016/S0040-4039(99)00537-7 | 0.622 | |||
| 1998 | Ma D, Ma Z, Kozikowski AP, Pshenichkin S, Wroblewski JT. Synthesis and biological evaluation of two analogues of (S)-alpha-methyl-3-carboxyphenylalanine. Bioorganic & Medicinal Chemistry Letters. 8: 2447-50. PMID 9873559 DOI: 10.1016/S0960-894X(98)00409-0 | 0.499 | |||
| 1998 | Ma D, Jiang J. Pd/Cu-catalyzed couplings of β-amino esters with aryl bromides. Synthesis of chiral 1,2,3,4-tetrahydro-4-oxo-2-alkyl-1-quinolines Tetrahedron-Asymmetry. 9: 1137-1142. DOI: 10.1016/S0957-4166(98)00078-0 | 0.44 | |||
| 1998 | Ma D, Jiang J. Polyfunctionalized pyrrolidinones via the coupling of N,N- disubstituted β-amino esters with ethyl glyoxalate Tetrahedron-Asymmetry. 9: 575-579. DOI: 10.1016/S0957-4166(98)00016-0 | 0.407 | |||
| 1998 | Ma D, Zhang J. Enantioselective syntheses of tussilagine and isotussilagine Tetrahedron Letters. 39: 9067-9068. DOI: 10.1016/S0040-4039(98)02076-0 | 0.485 | |||
| 1998 | Ma D, Tang W. Stereospecific synthesis of 9-substituted benzolactam-V8 from L-tyrosine via regioselective aromatic nitration Tetrahedron Letters. 39: 7369-7372. DOI: 10.1016/S0040-4039(98)01598-6 | 0.614 | |||
| 1997 | Kozikowski AP, Kotoula M, Ma D, Boujrad N, Tückmantel W, Papadopoulos V. Synthesis and biology of a 7-nitro-2,1,3-benzoxadiazol-4-yl derivative of 2-phenylindole-3-acetamide: a fluorescent probe for the peripheral-type benzodiazepine receptor. Journal of Medicinal Chemistry. 40: 2435-9. PMID 9258348 DOI: 10.1021/Jm970220W | 0.502 | |||
| 1997 | Kozikowski AP, Wang S, Ma D, Yao J, Ahmad S, Glazer RI, Bogi K, Acs P, Modarres S, Lewin NE, Blumberg PM. Modeling, chemistry, and biology of the benzolactam analogues of indolactam V (ILV). 2. Identification of the binding site of the benzolactams in the CRD2 activator-binding domain of PKCdelta and discovery of an ILV analogue of improved isozyme selectivity. Journal of Medicinal Chemistry. 40: 1316-26. PMID 9135029 DOI: 10.1021/Jm960875H | 0.496 | |||
| 1997 | Ma D, Tian H. Stereoselective synthesis of (S)-MPPG, (S)-MTPG and (S)-(+)-αM4CPG from (R)-4-hydroxyphenylglycine Journal of the Chemical Society-Perkin Transactions 1. 3493-3496. DOI: 10.1039/A704704E | 0.685 | |||
| 1997 | Ma D, Tian H, Sun H, Kozikowski AP, Pshenichkin S, Wroblewski JT. Synthesis and biological activity of cyclic analogues of MPPG and MCPG as metabotropic glutamate receptor antagonists Bioorganic and Medicinal Chemistry Letters. 7: 1195-1198. DOI: 10.1016/S0960-894X(97)00177-7 | 0.696 | |||
| 1997 | Ma D, Ma J, Dai L. Stereospecific Synthesis Of (1S,3R)-1-Aminocyclopentane-1,3-Dicarboxylic Acid, A Selective Agonist Of Metabotropic Glutamate Receptors Tetrahedron-Asymmetry. 8: 825-827. DOI: 10.1016/S0957-4166(97)00060-8 | 0.377 | |||
| 1997 | Ma D, Ma Z, Jiang J, Yang Z, Zheng C. Synthesis of (2S,1′ S,2′ S)-2-methyl-2-(carboxycyclopropyl)glycine and (S)-2-amino-2-methyl-4-phosphonobutyric acid from l-alanine Tetrahedron-Asymmetry. 8: 889-893. DOI: 10.1016/S0957-4166(97)00031-1 | 0.345 | |||
| 1997 | Ma D, Ma Z. Facile synthesis of (2S,1'S,2'S)-2-(carboxycyclopropyl)glycine an isotype-selective agonist of metabotropic glutamate receptors Tetrahedron Letters. 38: 7599-7602. DOI: 10.1016/S0040-4039(97)10037-5 | 0.35 | |||
| 1996 | Ma D, Yao J. Synthesis of chiral N-aryl-α-amino acids by PdCu catalyzed couplings of chiral α-amino acids with aryl halides Tetrahedron-Asymmetry. 7: 3075-3078. DOI: 10.1016/0957-4166(96)00401-6 | 0.449 | |||
| 1996 | Ma D, Ma J, Ding W, Dai L. An Improved Procedure To Homochiral Cyclic Statines Tetrahedron-Asymmetry. 7: 2365-2370. DOI: 10.1016/0957-4166(96)00291-1 | 0.399 | |||
| 1996 | Ma D, Tian H. Stereoselective synthesis of (S)-(+)-αM4CPG, a selective antagonist of metabotropic glutamate receptors Tetrahedron Asymmetry. 7: 1567-1570. DOI: 10.1016/0957-4166(96)00182-6 | 0.679 | |||
| 1995 | Kozikowski AP, Ma D, Du L, Lewin NE, Blumberg PM. Effect of Alteration of the Heterocyclic Nucleus of Indolactam V on Its Isoform Selectivity for PKC. Palladium-Catalyzed Route to Benzofuran Analogs of ILV Journal of the American Chemical Society. 117: 6666-6672. DOI: 10.1021/Ja00130A003 | 0.356 | |||
| 1994 | Kozikowski AP, Ma D, Du L, Lewin NE, Blumberg PM. A palladium catalyzed route to a benzofuran analogue of idolactam V (ILV): Effects on PKC isotype selectivity Pure and Applied Chemistry. 66: 2087-2090. DOI: 10.1351/Pac199466102087 | 0.585 | |||
| 1994 | Kozikowski AP, Ma D, Du L, Lewin NE, Blumberg PM. Synthesis of the benzofuran analogue of ILV, a new protein kinase C (PKC) activator Bioorganic & Medicinal Chemistry Letters. 4: 637-640. DOI: 10.1016/S0960-894X(01)80169-4 | 0.527 | |||
| 1993 | Kozikowski AP, Ma D, Pang YP, Shum P, Likic V, Mishra PK, Macura S, Basu A, Lazo JS, Ball RG. Synthesis, molecular modeling, 2-D NMR, and biological evaluation of ILV mimics as potential modulators of protein kinase C Journal of the American Chemical Society. 115: 3957-3965. DOI: 10.1021/Ja00063A015 | 0.553 | |||
| 1992 | Kozikowski AP, Ma D, Romeo E, Auta J, Papadopoulos V, Puia G, Costa E, Guidotti A. Synthesis of (2-Arylindol-3-yl)acetamides as Probes of Mitochondrial Steroidogenesis?A New Mechanism for GABAA Receptor Modulation Angewandte Chemie International Edition in English. 31: 1060-1062. DOI: 10.1002/Anie.199210601 | 0.484 | |||
| 1992 | Kozikowski AP, Ma D, Romeo E, Auta J, Papadopoulos V, Puia G, Costa E, Guidotti A. Synthese von (2-Arylindol-3-yl)acetamiden als Sonden zur Untersuchung der mitochondrialen Steroidbildung - ein neuer Mechanismus für die GABAA-Rezeptormodulation Angewandte Chemie. 104: 1092-1094. DOI: 10.1002/Ange.19921040837 | 0.449 | |||
| 1991 | Lu X, Guo C, Ma D. A new three-carbon homologating agent for synthesis of .gamma.-keto aldehydes The Journal of Organic Chemistry. 56: 6712-6714. DOI: 10.1021/Jo00023A044 | 0.58 | |||
| 1991 | Kozikowski AP, Ma D. Palladium catalyzed synthesis of annelated indoles Tetrahedron Letters. 32: 3317-3320. DOI: 10.1016/S0040-4039(00)92695-9 | 0.663 | |||
| 1990 | Lu X, Ma D. Stereoselective isomerization of acetylenic derivatives as a new methodology in organic synthesis Pure and Applied Chemistry. 62: 723-730. DOI: 10.1351/Pac199062040723 | 0.473 | |||
| 1990 | Lu X, Guo C, Ma D. A Convenient Synthesis of 3-(1,3-Alkadienyl)-2-cycloalken-1-ones Synlett. 1990: 357-358. DOI: 10.1055/S-1990-21094 | 0.663 | |||
| 1989 | Ma D, Yu Y, Lu X. Highly stereoselective isomerization of ynones to conjugated dienones catalyzed by transition-metal complexes The Journal of Organic Chemistry. 54: 1105-1109. DOI: 10.1021/Jo00266A021 | 0.546 | |||
| 1989 | Ma D, Lu X. Isomerization of propargylic alcohols catalyzed by an iridium complex Tetrahedron Letters. 30: 2109-2112. DOI: 10.1016/S0040-4039(01)93725-6 | 0.555 | |||
| 1989 | Ma D, Lu X. Facile synthesis of (2E,4E)-dienoic esters via stereoselective isomerization of 2-ynoic esters Tetrahedron Letters. 30: 843-844. DOI: 10.1016/S0040-4039(01)80631-6 | 0.597 | |||
| 1988 | Lu XY, Lin YQG, Ma DW. Novel reactions catalyzed by iridium pentahydride complex Pure and Applied Chemistry. 60: 1299-1306. DOI: 10.1351/pac198860081299 | 0.564 | |||
| 1988 | Ma D, Lin Y, Lu X, Yu Y. A novel stereoselective synthesis of conjugated dienones Tetrahedron Letters. 29: 1045-1048. DOI: 10.1016/0040-4039(88)85331-0 | 0.345 | |||
| 1988 | MA D, LIN Y, LU X, YU Y. ChemInform Abstract: A Novel Stereoselective Synthesis of Conjugated Dienones. Cheminform. 19. DOI: 10.1002/chin.198830102 | 0.371 | |||
| 1987 | Lin Y, Ma D, Lu X. Iridium pentahydride complex catalyzed dehydrogenation of alcohols in the absence of a hydrogen acceptor Tetrahedron Letters. 28: 3115-3118. DOI: 10.1016/S0040-4039(00)96299-3 | 0.544 | |||
| 1987 | lin Y, Ma D, Lu X. Selective cconversion of pinane into β-pinene catalyzed by an iridium pentahydride complex Journal of Organometallic Chemistry. 323: 407-409. DOI: 10.1016/0022-328X(87)80434-5 | 0.552 | |||
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