| Year |
Citation |
Score |
| 2021 |
Laroche B, Tang X, Archer G, Di Sanza R, Melchiorre P. Photochemical Chemoselective Alkylation of Tryptophan-Containing Peptides. Organic Letters. PMID 33400540 DOI: 10.1021/acs.orglett.0c03735 |
0.495 |
|
| 2019 |
Gandolfo E, Tang X, Raha Roy S, Melchiorre P. Photochemical Asymmetric Nickel-Catalyzed Acyl Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 31532568 DOI: 10.1002/Anie.201910168 |
0.626 |
|
| 2017 |
Tang X, Studer A. Alkene 1,2-difunctionalization via Radical Alkenyl Migration. Angewandte Chemie (International Ed. in English). PMID 29165859 DOI: 10.1002/Anie.201710397 |
0.467 |
|
| 2017 |
Tang X, Studer A. α-Perfluoroalkyl-β-alkynylation of alkenes via radical alkynyl migration. Chemical Science. 8: 6888-6892. PMID 29147514 DOI: 10.1039/C7Sc02175E |
0.444 |
|
| 2017 |
Liu Q, Tang X, Cai Y, Ma S. Catalytic One-Pot Synthesis of Trisubstituted Allenes from Terminal Alkynes and Ketones. Organic Letters. PMID 28905630 DOI: 10.1021/acs.orglett.7b02443 |
0.574 |
|
| 2017 |
Ma S, Liu Q, Tang X, Cai Y. Copper-Catalyzed Synthesis of Tetrasubstituted Allenes from Quaternary Ammonium Salts and Grignard Reagents Asian Journal of Organic Chemistry. 6: 1209-1212. DOI: 10.1002/Ajoc.201600620 |
0.586 |
|
| 2016 |
Tang X, Studer A. Sodium-Ketyl Radical Anions by Reverse Pinacol Reaction and Their Coupling with Iodoarenes. Organic Letters. PMID 27518325 DOI: 10.1021/Acs.Orglett.6B02184 |
0.458 |
|
| 2016 |
Han Y, Tang X, Cheng J, Ma S. Indium(III) Triflate-Catalyzed Efficient Prins-Type Cyclization of β-Allenols and Aldehydes Advanced Synthesis & Catalysis. 358: 4019-4029. DOI: 10.1002/Adsc.201600588 |
0.528 |
|
| 2015 |
Cai Y, Tang X, Ma S. Identifying a Highly Active Copper Catalyst for KA2 Reaction of Aromatic Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26660459 DOI: 10.1002/chem.201504823 |
0.584 |
|
| 2015 |
Tang X, Han Y, Ma S. Cadmium iodide mediated allenylation of terminal alkynes for the synthesis of methyl-substituted allenes. Organic Letters. 17: 1176-9. PMID 25674810 DOI: 10.1021/Acs.Orglett.5B00105 |
0.544 |
|
| 2015 |
Tang X, Huang X, Cao T, Han Y, Jiang X, Lin W, Tang Y, Zhang J, Yu Q, Fu C, Ma S. CuBr2-catalyzed enantioselective routes to highly functionalized and naturally occurring allenes Organic Chemistry Frontiers. 2: 688-691. DOI: 10.1039/C5Qo00084J |
0.543 |
|
| 2015 |
Kuang J, Tang X, Ma S. Zinc diiodide-promoted synthesis of trisubstituted allenes from propargylic amines Organic Chemistry Frontiers. 2: 470-475. DOI: 10.1039/C5Qo00047E |
0.583 |
|
| 2015 |
Kuang J, Tang X, Ma S. ChemInform Abstract: Zinc Diiodide-Promoted Synthesis of Trisubstituted Allenes from Propargylic Amines. Cheminform. 46: no-no. DOI: 10.1002/chin.201540080 |
0.532 |
|
| 2015 |
Tang X, Han Y, Ma S. ChemInform Abstract: Cadmium Iodide Mediated Allenylation of Terminal Alkynes for the Synthesis of Methyl-Substituted Allenes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201528085 |
0.385 |
|
| 2014 |
Lin W, Cao T, Fan W, Han Y, Kuang J, Luo H, Miao B, Tang X, Yu Q, Yuan W, Zhang J, Zhu C, Ma S. Enantioselective double manipulation of tetrahydroisoquinolines with terminal alkynes and aldehydes under copper(I) catalysis. Angewandte Chemie (International Ed. in English). 53: 277-81. PMID 24375740 DOI: 10.1002/Anie.201308699 |
0.634 |
|
| 2013 |
Tang X, Zhu C, Cao T, Kuang J, Lin W, Ni S, Zhang J, Ma S. Cadmium iodide-mediated allenylation of terminal alkynes with ketones. Nature Communications. 4: 2450. PMID 24042852 DOI: 10.1038/Ncomms3450 |
0.671 |
|
| 2013 |
Tang X, Kuang J, Ma S. CuBr for KA(2) reaction: en route to propargylic amines bearing a quaternary carbon center. Chemical Communications (Cambridge, England). 49: 8976-8. PMID 23962962 DOI: 10.1039/C3Cc45301D |
0.525 |
|
| 2013 |
Lü R, Ye J, Cao T, Chen B, Fan W, Lin W, Liu J, Luo H, Miao B, Ni S, Tang X, Wang N, Wang Y, Xie X, Yu Q, et al. Bimetallic enantioselective approach to axially chiral allenes. Organic Letters. 15: 2254-7. PMID 23607897 DOI: 10.1021/Ol400822M |
0.658 |
|
| 2013 |
Cheng J, Tang X, Ma S. Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes Acs Catalysis. 3: 663-666. DOI: 10.1021/cs300838k |
0.394 |
|
| 2013 |
Cheng J, Tang X, Yu Y, Ma S. ChemInform Abstract: FeCl3-Catalyzed Cyclization of α-Sulfonamido-Allenes with Aldehydes - The Substituent Effect. Cheminform. 44: no-no. DOI: 10.1002/chin.201316123 |
0.509 |
|
| 2012 |
Cheng J, Tang X, Yu Y, Ma S. FeCl3-catalyzed cyclization of α-sulfonamido-allenes with aldehydes--the substituent effect. Chemical Communications (Cambridge, England). 48: 12074-6. PMID 23135545 DOI: 10.1039/c2cc36941a |
0.56 |
|
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