Year |
Citation |
Score |
2025 |
Xu M, Wu K, He R, He J, Yang G, Ma H, Peng L, Zhang S, Tan L, Zhang Z, Cai Q. Design, synthesis and evaluation of (E)-1-(4-(2-(1H-pyrazol-5-yl)vinyl)phenyl) derivatives as next generation selective RET inhibitors overcoming RET solvent front mutations (G810C/R). European Journal of Medicinal Chemistry. 286: 117294. PMID 39879936 DOI: 10.1016/j.ejmech.2025.117294 |
0.311 |
|
2024 |
Ma H, Liu C, Li Z, Yu Q, Xiong H, Huang C, Tan L, Zhan M, Zhang Z, Cai Q. Discovery of the first examples of right open reading frame kinase 2 (RIOK2) molecular glue degraders. European Journal of Medicinal Chemistry. 283: 117166. PMID 39721086 DOI: 10.1016/j.ejmech.2024.117166 |
0.309 |
|
2024 |
Ao Y, Ma H, Gan B, Wang W, Zhang J, Zhou W, Zhang X, Cai Q. Copper-Catalyzed Asymmetric Kinugasa/Michael Addition Cascade Reactions for the Synthesis of Chiral Spiro β-Lactams. Organic Letters. PMID 38809099 DOI: 10.1021/acs.orglett.4c01568 |
0.348 |
|
2022 |
Zhong X, Huang M, Xiong H, Liang Y, Zhou W, Cai Q. Asymmetric Synthesis of Spiro[Azetidine-3,3'-Indoline]-2,2'-Diones via Copper(I)-Catalyzed Kinugasa/C-C Coupling Cascade Reaction. Angewandte Chemie (International Ed. in English). PMID 36053546 DOI: 10.1002/anie.202208323 |
0.433 |
|
2021 |
Ma H, Feng J, Zhou W, Chen C, Deng Z, Zhou F, Ouyang Y, Zhang X, Cai Q. Copper(i)-catalyzed asymmetric intramolecular C-arylation with ureas as the additives: highly enantioselective formation of spirooxindoles. Organic & Biomolecular Chemistry. 19: 7480-7484. PMID 34612367 DOI: 10.1039/d1ob01327k |
0.619 |
|
2021 |
Klionsky DJ, Abdel-Aziz AK, Abdelfatah S, Abdellatif M, Abdoli A, Abel S, Abeliovich H, Abildgaard MH, Abudu YP, Acevedo-Arozena A, Adamopoulos IE, Adeli K, Adolph TE, Adornetto A, Aflaki E, ... ... Cai Q, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy. 1-382. PMID 33634751 DOI: 10.1080/15548627.2020.1797280 |
0.543 |
|
2020 |
Liu J, Wang Y, Chen C, Tu Z, Zhu S, Zhou F, Si H, Zheng C, Zhang Z, Cai Q. Identification and Development of 1,4-Diaryl-1,2,3-triazolo-Based Ureas as Novel FLT3 Inhibitors. Acs Medicinal Chemistry Letters. 11: 1567-1572. PMID 32832025 DOI: 10.1021/acsmedchemlett.0c00216 |
0.45 |
|
2019 |
Liu T, Feng J, Chen C, Deng Z, Kotagiri R, Zhou G, Zhang X, Cai Q. Copper(I)-Catalyzed Intramolecular Asymmetric Double C-Arylation for the Formation of Chiral Spirocyclic Bis-oxindoles. Organic Letters. PMID 31184179 DOI: 10.1021/Acs.Orglett.9B01373 |
0.378 |
|
2019 |
Kotagiri R, Deng Z, Xu W, Cai Q. Stereospecific Synthesis of ( E)-5-Tetrasubstituted-ylidene-3,5-dihydro-4 H-imidazol-4-ones. Organic Letters. PMID 31140817 DOI: 10.1021/acs.orglett.9b01063 |
0.34 |
|
2018 |
Ding Q, He H, Cai Q. Chiral Aryliodine-Catalyzed Asymmetric Oxidative C-N Bond Formation via Desymmetrization Strategy. Organic Letters. PMID 30036067 DOI: 10.1021/acs.orglett.8b01849 |
0.346 |
|
2017 |
Zhang Y, Wang Q, Wang T, He H, Yang W, Zhang X, Cai Q. Enantioselective Synthesis of Chiral Oxygen-Containing Heterocycles Using Copper-Catalyzed Aryl C-O Coupling Reactions via Asymmetric Desymmetrization. The Journal of Organic Chemistry. PMID 28054776 DOI: 10.1021/Acs.Joc.6B02646 |
0.382 |
|
2017 |
An Y, He H, Liu T, Zhang Y, Lu X, Cai Q. Diversified Synthesis of 2-(4-Oxo[1,2,3]triazolo[1,5-a]quinoxalin-5(4H)-yl)acetamide Derivatives through Ugi-4-CR and Copper-Catalyzed Tandem Reactions Synthesis. 49: 3863-3873. DOI: 10.1055/S-0036-1590791 |
0.446 |
|
2016 |
Lu QP, Chen WD, Peng JR, Xu YD, Cai Q, Feng GK, Ding K, Zhu XF, Guan Z. Antitumor activity of 7RH, a discoidin domain receptor 1 inhibitor, alone or in combination with dasatinib exhibits antitumor effects in nasopharyngeal carcinoma cells. Oncology Letters. 12: 3598-3608. PMID 27900042 DOI: 10.3892/ol.2016.5088 |
0.359 |
|
2016 |
Zhou F, Liu J, Cai Q. ChemInform Abstract: Transition Metal Catalyzed Asymmetric Aryl Carbon-Heteroatom Bond Coupling Reactions Cheminform. 47. DOI: 10.1002/CHIN.201620247 |
0.564 |
|
2016 |
Liu J, Tian Y, Shi J, Zhang S, Cai Q. ChemInform Abstract: An Enantioselective Synthesis of Spirobilactams Through Copper-Catalyzed Intramolecular Double N-Arylation and Phase Separation. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201604137 |
0.378 |
|
2015 |
Zhou F, Cai Q. Recent advances in copper-catalyzed asymmetric coupling reactions. Beilstein Journal of Organic Chemistry. 11: 2600-15. PMID 26734106 DOI: 10.3762/bjoc.11.280 |
0.644 |
|
2015 |
Liu J, Tian Y, Shi J, Zhang S, Cai Q. An Enantioselective Synthesis of Spirobilactams through Copper-Catalyzed Intramolecular Double N-Arylation and Phase Separation. Angewandte Chemie (International Ed. in English). 54: 10917-20. PMID 26228798 DOI: 10.1002/anie.201504589 |
0.325 |
|
2015 |
Yang W, Liu Y, Zhang S, Cai Q. Copper-Catalyzed Intramolecular Desymmetric Aryl CO Coupling for the Enantioselective Construction of Chiral Dihydrobenzofurans and Dihydrobenzopyrans. Angewandte Chemie (International Ed. in English). 54: 8805-8. PMID 26060986 DOI: 10.1002/Anie.201503882 |
0.445 |
|
2015 |
He N, Huo Y, Liu J, Huang Y, Zhang S, Cai Q. Copper-catalyzed enantioselective intramolecular aryl C-N coupling: synthesis of enantioenriched 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an asymmetric desymmetrization strategy. Organic Letters. 17: 374-7. PMID 25547539 DOI: 10.1021/Ol5035386 |
0.587 |
|
2015 |
Yang W, Liu Y, Zhang S, Cai Q. ChemInform Abstract: Copper-Catalyzed Intramolecular Desymmetric Aryl C-O Coupling for the Enantioselective Construction of Chiral Dihydrobenzofurans and Dihydrobenzopyrans. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201548118 |
0.334 |
|
2015 |
He N, Huo Y, Liu J, Huang Y, Zhang S, Cai Q. ChemInform Abstract: Copper-Catalyzed Enantioselective Intramolecular Aryl C-N Coupling: Synthesis of Enantioenriched 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxamides via an Asymmetric Desymmetrization Strategy. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201523172 |
0.466 |
|
2015 |
Zhou F, Cheng G, Yang W, Long Y, Zhang S, Wu Y, Zhang X, Cai Q. ChemInform Abstract: Enantioselective Formation of Cyano-Bearing All-Carbon Quaternary Stereocenters: Desymmetrization by Copper-Catalyzed N-Arylation. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201508226 |
0.604 |
|
2014 |
Zhou F, Cheng GJ, Yang W, Long Y, Zhang S, Wu YD, Zhang X, Cai Q. Enantioselective formation of cyano-bearing all-carbon quaternary stereocenters: desymmetrization by copper-catalyzed N-arylation. Angewandte Chemie (International Ed. in English). 53: 9555-9. PMID 25045110 DOI: 10.1002/Anie.201405575 |
0.577 |
|
2014 |
Liu J, Yan J, Qin D, Cai Q. An Unexpected Inversion of Enantioselectivity in a Copper-Catalyzed Intramolecular Desymmetric Aryl C–N Coupling Reaction Synthesis. 46: 1917-1923. DOI: 10.1055/S-0033-1338638 |
0.475 |
|
2014 |
Liu J, Yan J, Qin D, Cai Q. ChemInform Abstract: An Unexpected Inversion of Enantioselectivity in a Copper-Catalyzed Intramolecular Desymmetric Aryl C-N Coupling Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201503128 |
0.518 |
|
2013 |
Yang W, Yan J, Long Y, Zhang S, Liu J, Zeng Y, Cai Q. Pd-catalyzed desymmetric intramolecular O-arylation reaction: enantioselective synthesis of (3,4-dihydro-2H-chromen-3-yl)methanols. Organic Letters. 15: 6022-5. PMID 24261632 DOI: 10.1021/ol402911y |
0.357 |
|
2013 |
Yang W, Long Y, Zhang S, Zeng Y, Cai Q. Copper-catalyzed enantioselective intramolecular N-arylation, an efficient method for kinetic resolutions. Organic Letters. 15: 3598-601. PMID 23829519 DOI: 10.1021/Ol401449B |
0.507 |
|
2013 |
Xu T, Zhang L, Xu S, Yang CY, Luo J, Ding F, Lu X, Liu Y, Tu Z, Li S, Pei D, Cai Q, Li H, Ren X, Wang S, et al. Pyrimido[4,5-d]pyrimidin-4(1H)-one derivatives as selective inhibitors of EGFR threonine790 to methionine790 (T790M) mutants. Angewandte Chemie (International Ed. in English). 52: 8387-90. PMID 23804305 DOI: 10.1002/Anie.201302313 |
0.415 |
|
2013 |
Yan X, Liao J, Lu Y, Liu J, Zeng Y, Cai Q. Pd-catalyzed one-pot synthesis of polysubstituted acrylamidines from isocyanides, diazo compounds, and imines. Organic Letters. 15: 2478-81. PMID 23642149 DOI: 10.1021/Ol4009552 |
0.426 |
|
2013 |
Cai Q, Zhou F. Development and challenges in copper-catalyzed asymmetric Ullmann-type coupling reactions Synlett. 24: 408-411. DOI: 10.1055/S-0032-1317866 |
0.687 |
|
2013 |
Yang W, Long Y, Zhang S, Zeng Y, Cai Q. ChemInform Abstract: Copper-Catalyzed Enantioselective Intramolecular N-Arylation, an Efficient Method for Kinetic Resolution. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201350169 |
0.395 |
|
2013 |
Zhou F, Guo J, Liu J, Ding K, Yu S, Cai Q. ChemInform Abstract: Copper-Catalyzed Desymmetric Intramolecular Ullmann C-N Coupling: An Enantioselective Preparation of Indolines. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201309128 |
0.646 |
|
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 |
0.793 |
|
2012 |
Cai Q, Yan J, Ding K. A CuAAC/Ullmann C-C coupling tandem reaction: copper-catalyzed reactions of organic azides with N-(2-iodoaryl)propiolamides or 2-iodo-N-(prop-2-ynyl)benzenamines. Organic Letters. 14: 3332-5. PMID 22724380 DOI: 10.1021/Ol301307X |
0.644 |
|
2012 |
Yan J, Zhou F, Qin D, Cai T, Ding K, Cai Q. Synthesis of [1,2,3]triazolo[1,5-a]quinoxalin-4(5H)-ones through copper-catalyzed tandem reactions of N-(2-haloaryl)propiolamides with sodium azide. Organic Letters. 14: 1262-5. PMID 22335274 DOI: 10.1021/Ol300114W |
0.743 |
|
2012 |
Peng Y, Sun H, Lu J, Liu L, Cai Q, Shen R, Yang CY, Yi H, Wang S. Bivalent Smac mimetics with a diazabicyclic core as highly potent antagonists of XIAP and cIAP1/2 and novel anticancer agents. Journal of Medicinal Chemistry. 55: 106-14. PMID 22148838 DOI: 10.1021/Jm201072X |
0.496 |
|
2012 |
Cai Q, Yan J, Ding K. ChemInform Abstract: A CuAAC/Ullmann C-C Coupling Tandem Reaction: Copper-Catalyzed Reactions of Organic Azides with N-(2-Iodoaryl)propiolamides or 2-Iodo-N-(prop-2-ynyl)benzenamines. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201244153 |
0.482 |
|
2012 |
Yan J, Zhou F, Qin D, Cai T, Ding K, Cai Q. ChemInform Abstract: Synthesis of [1,2,3]Triazolo[1,5-a]quinoxalin-4(5H)-ones Through Copper-Catalyzed Tandem Reactions of N-(2-Haloaryl)propiolamides with Sodium Azide. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201227169 |
0.652 |
|
2012 |
Zhou F, Ding K, Cai Q. ChemInform Abstract: Palladium-Catalyzed Amidation of N-Tosylhydrazones with Isocyanides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201211061 |
0.617 |
|
2011 |
Zhou F, Ding K, Cai Q. Palladium-catalyzed amidation of N-tosylhydrazones with isocyanides. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12268-71. PMID 21938752 DOI: 10.1002/Chem.201102459 |
0.701 |
|
2011 |
Zhou F, Liu J, Ding K, Liu J, Cai Q. Copper-catalyzed tandem reaction of isocyanides with N-(2-haloaryl)propiolamides for the synthesis of pyrrolo[3,2-c]quinolin-4-ones. The Journal of Organic Chemistry. 76: 5346-53. PMID 21591728 DOI: 10.1021/Jo2006939 |
0.743 |
|
2011 |
Cai Q, Sun H, Peng Y, Lu J, Nikolovska-Coleska Z, McEachern D, Liu L, Qiu S, Yang CY, Miller R, Yi H, Zhang T, Sun D, Kang S, Guo M, et al. A potent and orally active antagonist (SM-406/AT-406) of multiple inhibitor of apoptosis proteins (IAPs) in clinical development for cancer treatment. Journal of Medicinal Chemistry. 54: 2714-26. PMID 21443232 DOI: 10.1021/Jm101505D |
0.485 |
|
2011 |
Wang D, Zhang Z, Lu X, Feng Y, Luo K, Gan J, Yingxue L, Wan J, Li X, Zhang F, Tu Z, Cai Q, Ren X, Ding K. Hybrid compounds as new Bcr/Abl inhibitors. Bioorganic & Medicinal Chemistry Letters. 21: 1965-8. PMID 21376587 DOI: 10.1016/J.Bmcl.2011.02.029 |
0.444 |
|
2011 |
Cai Q, Zhou F, Xu T, Fu L, Ding K. Copper-catalyzed tandem reactions of 1-(2-iodoary)-2-yn-1-ones with isocyanides for the synthesis of 4-oxo-indeno[1,2-b]pyrroles. Organic Letters. 13: 340-343. PMID 21162591 DOI: 10.1021/Ol102826F |
0.722 |
|
2011 |
Cai Q, Zhou F, Fu L, Wie J, Ding K. Synthesis of 4-Oxoindeno[1,2-b]pyrroles through Copper-Catalyzed Tandem Reactions of 1-(2-Haloaryl)enones with Isocyanides Synthesis. 2011: 3037-3044. DOI: 10.1055/S-0030-1260171 |
0.655 |
|
2011 |
Gao M, Liu X, Wang X, Cai Q, Ding K. Synthesis of 1-Aryl-1H-indazoles via a Ligand-Free Copper- Catalyzed Intramolecular Amination Reaction Chinese Journal of Chemistry. 29: 1199-1204. DOI: 10.1002/Cjoc.201190223 |
0.517 |
|
2011 |
Zhou F, Fu L, Wie J, Ding K, Cai Q. ChemInform Abstract: Synthesis of 4-Oxoindeno[1,2-b]pyrroles Through Copper-Catalyzed Tandem Reactions of 1-(2-Haloaryl)enones with Isocyanides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201204099 |
0.62 |
|
2011 |
Zhou F, Liu J, Ding K, Liu J, Cai Q. ChemInform Abstract: Copper-Catalyzed Tandem Reaction of Isocyanides with N-(2-Haloaryl)propiolamides for the Synthesis of Pyrrolo[3,2-c]quinolin-4-ones. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201148159 |
0.684 |
|
2011 |
Gao M, Liu X, Wang X, Cai Q, Ding K. ChemInform Abstract: Synthesis of 1-Aryl-1H-indazoles via a Ligand-Free Copper-Catalyzed Intramolecular Amination Reaction. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201146122 |
0.403 |
|
2011 |
Cai Q, Zhou F, Xu T, Fu L, Ding K. ChemInform Abstract: Copper-Catalyzed Tandem Reactions of 1-(2-Iodoaryl)-2-yn-1-ones with Isocyanides for the Synthesis of 4-Oxo-indeno[1,2-b]pyrroles. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201116112 |
0.621 |
|
2010 |
Cai Q, Li Z, Wei J, Fu L, Ha C, Pei D, Ding K. Synthesis of aza-fused polycyclic quinolines through copper-catalyzed cascade reactions. Organic Letters. 12: 1500-3. PMID 20196570 DOI: 10.1021/Ol1002225 |
0.661 |
|
2010 |
Cai Q, Ding K, Li Z, Fu L, Wei J, Ha C, Pei D. A Room-Temperature, Copper-Catalyzed Cascade Process for Diethyl 2-Aryl-3,4-dihydro-4-oxo-1,1(2H)-naphthalenedicarboxylate Synthesis. 2010: 3289-3294. DOI: 10.1055/S-0030-1257937 |
0.397 |
|
2010 |
Chen H, Wang D, Wang X, Huang W, Cai Q, Ding K. Mild Conditions for Copper-CatalyzedN-Arylation of Imidazoles Synthesis. 2010: 1505-1511. DOI: 10.1055/S-0029-1218691 |
0.507 |
|
2010 |
Cai Q, Li Z, Wei J, Fu L, Ha C, Pei D, Ding K. ChemInform Abstract: Synthesis of Aza-Fused Polycyclic Quinolines Through Copper-Catalyzed Cascade Reactions. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201033154 |
0.433 |
|
2010 |
Wang D, Cai Q, Ding K. ChemInform Abstract: An Efficient Copper-Catalyzed Amination of Aryl Halides by Aqueous Ammonia. Cheminform. 41. DOI: 10.1002/CHIN.201002071 |
0.35 |
|
2009 |
Cai Q, Li Z, Wei J, Ha C, Pei D, Ding K. Assembly of indole-2-carboxylic acid esters through a ligand-free copper-catalysed cascade process. Chemical Communications (Cambridge, England). 7581-3. PMID 20024286 DOI: 10.1039/B918345K |
0.603 |
|
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 |
0.808 |
|
2009 |
Cai Q, Zhang H, Zou B, Xie X, Zhu W, He G, Wang J, Pan X, Chen Y, Yuan Q, et al. ea. ChemInform Abstract: Amino Acid Promoted Ullmann-Type Coupling Reactions and Their Applications in Organic Synthesis Cheminform. 40. DOI: 10.1002/CHIN.200933243 |
0.716 |
|
2009 |
Wang D, Cai Q, Ding K. An Efficient Copper-Catalyzed Amination of Aryl Halides by Aqueous Ammonia Advanced Synthesis & Catalysis. 351: 1722-1726. DOI: 10.1002/Adsc.200900327 |
0.505 |
|
2008 |
Peng Y, Sun H, Nikolovska-Coleska Z, Qiu S, Yang CY, Lu J, Cai Q, Yi H, Kang S, Yang D, Wang S. Potent, orally bioavailable diazabicyclic small-molecule mimetics of second mitochondria-derived activator of caspases. Journal of Medicinal Chemistry. 51: 8158-62. PMID 19049347 DOI: 10.1021/Jm801254R |
0.488 |
|
2008 |
Sun H, Nikolovska-Coleska Z, Yang CY, Qian D, Lu J, Qiu S, Bai L, Peng Y, Cai Q, Wang S. Design of small-molecule peptidic and nonpeptidic Smac mimetics. Accounts of Chemical Research. 41: 1264-77. PMID 18937395 DOI: 10.1021/Ar8000553 |
0.496 |
|
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 |
0.677 |
|
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 |
0.697 |
|
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 |
0.6 |
|
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 |
0.683 |
|
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 |
0.667 |
|
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 |
0.551 |
|
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 |
0.635 |
|
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 |
0.784 |
|
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 |
0.645 |
|
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 |
0.644 |
|
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 |
0.68 |
|
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