| Year |
Citation |
Score |
| 2023 |
Liu Z, Gao B, Chernichenko K, Yang H, Lemaire S, Tang W. Enantioselective C-H Arylation for Axially Chiral Heterobiaryls. Organic Letters. 25: 7004-7008. PMID 37708038 DOI: 10.1021/acs.orglett.3c02478 |
0.402 |
|
| 2023 |
Tao Y, Xia W, Zhao Q, Xiang H, Han C, Zhang S, Gu W, Tang W, Li Y, Tan L, Li D, Liu C. Structural mechanism for specific binding of chemical compounds to amyloid fibrils. Nature Chemical Biology. PMID 37400537 DOI: 10.1038/s41589-023-01370-x |
0.313 |
|
| 2023 |
Sun J, Chen Y, Ragab SS, Gu W, Tang Z, Tang Y, Tang W. Total Syntheses of Polyhydroxylated Steroids by an Unsaturation-Functionalization Strategy. Angewandte Chemie (International Ed. in English). e202303639. PMID 37084230 DOI: 10.1002/anie.202303639 |
0.364 |
|
| 2023 |
Zhou M, Lin Y, Chen XX, Xu G, Chung LW, Tang W. Asymmetric Synthesis of Vicinal Tetrasubstituted Diamines via Reductive Coupling of Ketimines Templated by Chiral Diborons. Angewandte Chemie (International Ed. in English). e202300334. PMID 36859620 DOI: 10.1002/anie.202300334 |
0.435 |
|
| 2023 |
Zhu J, Li Z, Li J, Tian D, Xu R, Tan Z, Chen Z, Tang W. Enantioselective rhodium-catalyzed addition of arylboronic acids to -heteroaryl ketones: synthesis of α-hydroxy acids. Chemical Science. 14: 1606-1612. PMID 36794198 DOI: 10.1039/d2sc05907j |
0.377 |
|
| 2022 |
Yang H, Tang W. Enantioselective construction of ortho-sulfur- or nitrogen-substituted axially chiral biaryls and asymmetric synthesis of isoplagiochin D. Nature Communications. 13: 4577. PMID 35931694 DOI: 10.1038/s41467-022-32360-7 |
0.452 |
|
| 2022 |
Li B, Luo B, Yang H, Tang W. Heck Reaction of N-Heteroaryl Halides for the Concise Synthesis of Chiral α-Heteroaryl-substituted Heterocycles. Angewandte Chemie (International Ed. in English). e202209087. PMID 35876722 DOI: 10.1002/anie.202209087 |
0.421 |
|
| 2022 |
Zhu M, Wang P, Zhang Q, Tang W, Zi W. Diastereodivergent Aldol-Type Coupling of Alkoxyallenes with Pentafluorophenyl Esters Enabled by Synergistic Palladium/Chiral Lewis Base Catalysis. Angewandte Chemie (International Ed. in English). PMID 35713176 DOI: 10.1002/anie.202207621 |
0.759 |
|
| 2022 |
Li Z, Xu R, Guo H, Yang H, Xu G, Shi E, Xiao J, Tang W. Enantioselective Rhodium-Catalyzed Hydrogenation of ()--Sulfonyl-α-dehydroamido Boronic Esters. Organic Letters. PMID 34978454 DOI: 10.1021/acs.orglett.1c04157 |
0.381 |
|
| 2021 |
Li B, Luo B, Blakemore CA, Smith AC, Widlicka DW, Berritt S, Tang W. Synthesis of α-Heteroaryl Propionic Esters by Palladium-Catalyzed α-Heteroarylation of Silyl Ketene Acetals. Organic Letters. PMID 34369790 DOI: 10.1021/acs.orglett.1c02257 |
0.318 |
|
| 2021 |
Wan F, Wang N, Zhu Y, Tang C, Claverie J, Tang W. Enantioselective hydrogenation of cyclic tetrasubstituted-olefinic dehydroamino acid derivatives. Chemical Communications (Cambridge, England). PMID 33969835 DOI: 10.1039/d1cc01277k |
0.377 |
|
| 2021 |
Xu R, Gao Z, Yu Y, Tang Y, Tian D, Chen T, Chen Y, Xu G, Shi E, Tang W. A facile and practical preparation of -chiral phosphine oxides. Chemical Communications (Cambridge, England). PMID 33665653 DOI: 10.1039/d1cc00646k |
0.305 |
|
| 2020 |
Tang W, Tian D, Xu R, Zhu J, Huang J, Dong W, Claverie J. Asymmetric Hydroesterification of Diarylmethyl Carbinols. Angewandte Chemie (International Ed. in English). PMID 33326671 DOI: 10.1002/anie.202015450 |
0.343 |
|
| 2020 |
Li B, Aliyu MA, Gao Z, Li T, Dong W, Li J, Shi E, Tang W. General Synthesis of Chiral α,α-Diaryl Carboxamides by Enantioselective Palladium-Catalyzed Cross-Coupling. Organic Letters. 22: 4974-4978. PMID 32610916 DOI: 10.1021/Acs.Orglett.0C01489 |
0.48 |
|
| 2020 |
Wu T, Kang X, Bai H, Xiong W, Xu G, Tang W. Enantioselective Construction of Spiro Quaternary Carbon Stereocenters via Pd-Catalyzed Intramolecular α-Arylation. Organic Letters. PMID 32484358 DOI: 10.1021/Acs.Orglett.0C01129 |
0.486 |
|
| 2020 |
Zhou M, Li K, Chen D, Xu R, Xu G, Tang W. Enantioselective Reductive Coupling of Imines Templated by Chiral Diboron. Journal of the American Chemical Society. PMID 32459089 DOI: 10.1021/Jacs.0C04558 |
0.522 |
|
| 2020 |
Qian C, Tang W. A Versatile Synthesis of Vinyl-Substituted Heterocycles via Regio- and Enantioselective Pd-Catalyzed Tandem Allylic Substitution. Organic Letters. PMID 32453581 DOI: 10.1021/Acs.Orglett.0C01490 |
0.526 |
|
| 2020 |
Yang H, Sun J, Gu W, Tang W. Enantioselective Cross-Coupling for Axially Chiral Tetra-ortho-Substituted Biaryls and Asymmetric Synthesis of Gossypol. Journal of the American Chemical Society. PMID 32240585 DOI: 10.1021/Jacs.0C02686 |
0.549 |
|
| 2020 |
Tang W, Mu X, Yu H, Peng H, Xiong W, Wu T. Expedite Construction of Various Bridged Polycyclic Skeletons by Palladium-Catalyzed Dearomatization. Angewandte Chemie (International Ed. in English). PMID 32061117 DOI: 10.1002/Anie.202000953 |
0.505 |
|
| 2020 |
Xu R, Yang H, Tang W. Efficient Synthesis of Chiral Drugs Facilated by P-Chiral Phosphorus Ligands Chinese Journal of Organic Chemistry. 40: 1409. DOI: 10.6023/Cjoc202003015 |
0.463 |
|
| 2020 |
Qian C, Tang W. NiH-Catalyzed Migratory Defluorinative Olefin Cross-Coupling: Trifluoromethyl-Substituted Alkenes as Acceptor Olefins to Form gem-Difluoroalkenes Chinese Journal of Organic Chemistry. 40: 1076. DOI: 10.6023/cjoc202000017 |
0.318 |
|
| 2020 |
Liu Z, Li T, Zhao J, Tang W. A substituted tricyclohexylphosphane with “conformational lock” Tetrahedron. 76: 131216. DOI: 10.1016/J.Tet.2020.131216 |
0.426 |
|
| 2019 |
Li C, Ragab SS, Liu G, Tang W. Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update. Natural Product Reports. PMID 31515549 DOI: 10.1039/C9Np00039A |
0.793 |
|
| 2019 |
Tang W, Zhu J, Huang L, Dong W, Li N, Yu X, Deng WP. Enantioselective Rhodium-Catalyzed Addition of Arylboroxines to N-Unprotected Ketimines: Efficient Synthesis of Cipargamin. Angewandte Chemie (International Ed. in English). PMID 31468680 DOI: 10.1002/Anie.201910008 |
0.497 |
|
| 2019 |
Tang W. Stereoelectronic Effect in Ligand Design: Enantioselective Rh-Catalyzed Hydrogenation of Alkyl Cyclic Tetrasubstituted Enamides and Concise Synthesis of (R)-Tofacitinib. Angewandte Chemie (International Ed. in English). PMID 31343811 DOI: 10.1002/Anie.201908089 |
0.533 |
|
| 2019 |
Tang W. Enantioselective Palladium-Catalyzed Cross-Coupling between α-Bromo Carboxamides and Arylboronic Acids. Angewandte Chemie (International Ed. in English). PMID 31140685 DOI: 10.1002/Anie.201905174 |
0.479 |
|
| 2019 |
Yang H, Tang W. Efficient Enantioselective Syntheses of Chiral Natural Products Facilitated by Ligand Design. Chemical Record (New York, N.Y.). PMID 31025478 DOI: 10.1002/Tcr.201900003 |
0.522 |
|
| 2019 |
Xu G, Senanayake CH, Tang W. P-Chiral Phosphorus Ligands Based on a 2,3-Dihydrobenzo[ d][1,3]oxaphosphole Motif for Asymmetric Catalysis. Accounts of Chemical Research. PMID 30848882 DOI: 10.1021/Acs.Accounts.9B00029 |
0.546 |
|
| 2019 |
Xiong W, Xu G, Yu X, Tang W. P-Chiral Monophosphorus Ligands for Asymmetric Copper-Catalyzed Allylic Alkylation Organometallics. 38: 4003-4013. DOI: 10.1021/Acs.Organomet.9B00194 |
0.497 |
|
| 2019 |
Dong W, Xu G, Tang W. Enantioselective palladium-catalyzed C(sp2)-H carbamoylation Tetrahedron. 75: 3239-3247. DOI: 10.1016/J.Tet.2019.03.038 |
0.515 |
|
| 2019 |
Wu Z, Si T, Xu G, Xu B, Tang W. Ligand-free nickel-catalyzed Kumada couplings of aryl bromides with tert-butyl Grignard reagents Chinese Chemical Letters. 30: 597-600. DOI: 10.1016/J.Cclet.2018.12.027 |
0.452 |
|
| 2018 |
Tang W, Rao X, Li N, Bai H, Wang Z. Efficient Synthesis of (-)-Corynoline by Sterically Hindered Enantioselective Palladium-Catalyzed α-Arylation. Angewandte Chemie (International Ed. in English). PMID 30074668 DOI: 10.1002/Anie.201807302 |
0.541 |
|
| 2018 |
Deng H, Yang WL, Tian F, Tang W, Deng WP. Asymmetric Construction of 3-Azabicyclo[3.1.0]hexane Skeleton with Five Contiguous Stereogenic Centers by Cu-Catalyzed 1,3-Dipolar Cycloaddition of Trisubstituted Cyclopropenes. Organic Letters. PMID 29943995 DOI: 10.1021/Acs.Orglett.8B01686 |
0.398 |
|
| 2018 |
Tang W, Tian D, Li C, Gu G, Zhang X, Peng H. Stereospecific Nucleophilic Substitution with Arylboronic Acids as Nucleophiles: A Crucial CONH Effect. Angewandte Chemie (International Ed. in English). PMID 29687594 DOI: 10.1002/Anie.201712829 |
0.766 |
|
| 2018 |
Cheng R, Li B, Wu J, Zhang J, Qiu Z, Tang W, You SL, Tang Y, Xie Z. Enantioselective Synthesis of Chiral-at-Cage o-Carboranes via Pd-Catalyzed Asymmetric B-H Substitution. Journal of the American Chemical Society. PMID 29575894 DOI: 10.1021/Jacs.8B01754 |
0.518 |
|
| 2018 |
Tian D, Peng H, Liu Z, Tang W. Optically active N-alkyl aziridines via stereospecific reductive cyclization of α-mesylated acetamides Organic Chemistry Frontiers. 5: 2723-2727. DOI: 10.1039/C8Qo00774H |
0.357 |
|
| 2018 |
Liu G, Fu W, Mu X, Wu T, Nie M, Li K, Xu X, Tang W. Pyrrolidines and piperidines bearing chiral tertiary alcohols by nickel-catalyzed enantioselective reductive cyclization of N-alkynones Communications Chemistry. 1. DOI: 10.1038/s42004-018-0092-1 |
0.783 |
|
| 2018 |
Zhou Q, Tang W, Chung LW. Mechanistic insights into asymmetric reductive coupling of isoquinolines by a chiral diboron with DFT calculations Journal of Organometallic Chemistry. 864: 97-104. DOI: 10.1016/J.Jorganchem.2018.02.001 |
0.398 |
|
| 2018 |
Jiang W, Zhao Q, Tang W. Efficient P-Chiral Biaryl Bisphosphorus Ligands for Palladium-Catalyzed Asymmetric Hydrogenation Chinese Journal of Chemistry. 36: 153-156. DOI: 10.1002/Cjoc.201700645 |
0.498 |
|
| 2017 |
Jin JH, Wang H, Yang ZT, Yang WL, Tang W, Deng WP. Asymmetric Synthesis of 3,4-Dihydroquinolin-2-ones via a Stereoselective Palladium-Catalyzed Decarboxylative [4 + 2]- Cycloaddition. Organic Letters. PMID 29227662 DOI: 10.1021/Acs.Orglett.7B03467 |
0.569 |
|
| 2017 |
Si T, Li B, Xiong W, Xu B, Tang W. Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids. Organic & Biomolecular Chemistry. PMID 29159328 DOI: 10.1039/C7Ob02531A |
0.472 |
|
| 2017 |
Du K, Yang H, Guo P, Feng L, Xu G, Zhou Q, Chung LW, Tang W. Efficient syntheses of (-)-crinine and (-)-aspidospermidine, and the formal synthesis of (-)-minfiensine by enantioselective intramolecular dearomative cyclization. Chemical Science. 8: 6247-6256. PMID 28989658 DOI: 10.1039/C7Sc01859B |
0.725 |
|
| 2017 |
Liu J, Nie M, Zhou Q, Gao S, Jiang W, Chung LW, Tang W, Ding K. Enantioselective palladium-catalyzed diboration of 1,1-disubstituted allenes. Chemical Science. 8: 5161-5165. PMID 28970901 DOI: 10.1039/C7Sc01254C |
0.549 |
|
| 2017 |
Chen D, Xu G, Zhou Q, Chung LW, Tang W. A Practical and Asymmetric Reductive Coupling of Isoquinolines Templated by Chiral Diborons. Journal of the American Chemical Society. PMID 28700227 DOI: 10.1021/Jacs.7B04256 |
0.524 |
|
| 2017 |
Zhang Z, Wang J, Li J, Yang F, Liu G, Tang W, He W, Fu JJ, Shen YH, Li A, Zhang WD. Total Synthesis and Stereochemical Assignment of Delavatine A: Rh-Catalyzed Asymmetric Hydrogenation of Indene-Type Tetrasubstituted Olefins and Kinetic Resolution through Pd-Catalyzed Triflamide-Directed C-H Olefination. Journal of the American Chemical Society. PMID 28271887 DOI: 10.1021/Jacs.7B01718 |
0.801 |
|
| 2017 |
Zhao G, Xu G, Qian C, Tang W. Efficient Enantioselective Syntheses of (+)-Dalesconol A and B. Journal of the American Chemical Society. PMID 28225267 DOI: 10.1021/Jacs.7B00783 |
0.479 |
|
| 2016 |
Wei X, Qu B, Zeng X, Savoie J, Fandrick KR, Desrosiers JN, Tcyrulnikov S, Marsini MA, Buono FG, Li Z, Yang BS, Tang W, Haddad N, Gutierrez O, Wang J, et al. Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor. Journal of the American Chemical Society. PMID 27794616 DOI: 10.1021/Jacs.6B09764 |
0.509 |
|
| 2016 |
Li C, Zhang Y, Sun Q, Gu T, Peng H, Tang W. Transition-Metal-Free Stereospecific Cross-Coupling with Alkenylboronic Acids as Nucleophiles. Journal of the American Chemical Society. PMID 27515390 DOI: 10.1021/Jacs.6B06285 |
0.669 |
|
| 2016 |
Hu N, Li K, Wang Z, Tang W. Synthesis of Chiral 1,4-Benzodioxanes and Chromans by Enantioselective Palladium-Catalyzed Alkene Aryloxyarylation Reactions. Angewandte Chemie (International Ed. in English). PMID 26990370 DOI: 10.1002/Anie.201600379 |
0.533 |
|
| 2016 |
Huang L, Zhu J, Jiao G, Wang Z, Yu X, Deng WP, Tang W. Highly Enantioselective Rhodium-Catalyzed Addition of Arylboroxines to Simple Aryl Ketones: Efficient Synthesis of Escitalopram. Angewandte Chemie (International Ed. in English). PMID 26933831 DOI: 10.1002/Anie.201600979 |
0.355 |
|
| 2016 |
Li C, Chen D, Tang W. Addressing the Challenges in Suzuki-Miyaura Cross-Couplings by Ligand Design Synlett. 27: 2183-2200. DOI: 10.1055/S-0035-1562360 |
0.496 |
|
| 2016 |
Fu W, Tang W. Chiral Monophosphorus Ligands for Asymmetric Catalytic Reactions Acs Catalysis. 6: 4814-4858. DOI: 10.1021/Acscatal.6B01001 |
0.532 |
|
| 2016 |
Yang H, Yang X, Tang W. Transition-metal catalyzed asymmetric carbon–carbon cross-coupling with chiral ligands Tetrahedron. 72: 6143-6174. DOI: 10.1016/J.Tet.2016.08.042 |
0.409 |
|
| 2016 |
Cao Z, Du K, Liu J, Tang W. Synthesis of triptoquinone H and its C-5 epimer via efficient asymmetric dearomative cyclization Tetrahedron. 72: 1782-1786. DOI: 10.1016/J.Tet.2016.02.043 |
0.535 |
|
| 2016 |
Yang X, Xu G, Tang W. Efficient synthesis of chiral biaryls via asymmetric Suzuki-Miyaura cross-coupling of ortho-bromo aryl triflates Tetrahedron. 72: 5178-5183. DOI: 10.1016/J.Tet.2015.12.051 |
0.527 |
|
| 2015 |
Fandrick KR, Li W, Zhang Y, Tang W, Gao J, Rodriguez S, Patel ND, Reeves DC, Wu JP, Sanyal S, Gonnella N, Qu B, Haddad N, Lorenz JC, Sidhu K, et al. Concise and Practical Asymmetric Synthesis of a Challenging Atropisomeric HIV Integrase Inhibitor. Angewandte Chemie (International Ed. in English). 54: 7144-8. PMID 25939331 DOI: 10.1002/Anie.201501575 |
0.464 |
|
| 2015 |
Hu N, Zhao G, Zhang Y, Liu X, Li G, Tang W. Synthesis of Chiral α-Amino Tertiary Boronic Esters by Enantioselective Hydroboration of α-Arylenamides. Journal of the American Chemical Society. 137: 6746-9. PMID 25938599 DOI: 10.1021/Jacs.5B03760 |
0.462 |
|
| 2015 |
Du K, Guo P, Chen Y, Cao Z, Wang Z, Tang W. Enantioselective palladium-catalyzed dearomative cyclization for the efficient synthesis of terpenes and steroids. Angewandte Chemie (International Ed. in English). 54: 3033-7. PMID 25631391 DOI: 10.1002/Anie.201411817 |
0.712 |
|
| 2015 |
Li C, Chen T, Li B, Xiao G, Tang W. Efficient synthesis of sterically hindered arenes bearing acyclic secondary alkyl groups by Suzuki-Miyaura cross-couplings. Angewandte Chemie (International Ed. in English). 54: 3792-6. PMID 25630668 DOI: 10.1002/Anie.201411518 |
0.727 |
|
| 2015 |
Fu W, Nie M, Wang A, Cao Z, Tang W. Highly enantioselective nickel-catalyzed intramolecular reductive cyclization of alkynones. Angewandte Chemie (International Ed. in English). 54: 2520-4. PMID 25597850 DOI: 10.1002/Anie.201410700 |
0.557 |
|
| 2015 |
Lautens M, Le CM, Du K, Guo P, Chen Y, Cao Z, Wang Z, Tang W. Palladium-Catalyzed Enantioselective Dearomative Cyclization of Phenols Synfacts. 11: 393-393. DOI: 10.1055/S-0034-1380394 |
0.535 |
|
| 2015 |
Lautens M, Le CM, Fu W, Nie M, Wang A, Cao Z, Tang W. Nickel-Catalyzed Enantioselective Reductive Cyclizations of Alkynones Synfacts. 11: 392-392. DOI: 10.1055/S-0034-1380392 |
0.519 |
|
| 2015 |
Nie M, Fu W, Cao Z, Tang W. Enantioselective nickel-catalyzed alkylative alkyne-aldehyde cross-couplings Organic Chemistry Frontiers. 2: 1322-1325. DOI: 10.1039/C5Qo00148J |
0.543 |
|
| 2015 |
Xu G, Li M, Wang S, Tang W. Efficient synthesis of P-chiral biaryl phosphonates by stereoselective intramolecular cyclization Organic Chemistry Frontiers. 2: 1342-1345. DOI: 10.1039/C5Qo00142K |
0.523 |
|
| 2014 |
Xu G, Fu W, Liu G, Senanayake CH, Tang W. Efficient syntheses of korupensamines A, B and michellamine B by asymmetric Suzuki-Miyaura coupling reactions. Journal of the American Chemical Society. 136: 570-3. PMID 24147559 DOI: 10.1021/Ja409669R |
0.812 |
|
| 2014 |
Xu G, Zhao Q, Tang W. Development of Efficient Asymmetric Suzuki-Miyaura Cross-Coupling and Applications in Synthesis Chinese Journal of Organic Chemistry. 34: 1919. DOI: 10.6023/Cjoc201406030 |
0.523 |
|
| 2014 |
Li C, Xiao G, Zhao Q, Liu H, Wang T, Tang W. Sterically demanding aryl–alkyl Suzuki–Miyaura coupling Org. Chem. Front.. 1: 225-229. DOI: 10.1039/C4Qo00024B |
0.427 |
|
| 2014 |
Reeves JT, Tan Z, Reeves DC, Song JJ, Han ZS, Xu Y, Tang W, Yang BS, Razavi H, Harcken C, Kuzmich D, Mahaney PE, Lee H, Busacca CA, Senanayake CH. Development of an enantioselective hydrogenation route to (S)-1-(2-(methylsulfonyl)pyridin-4-yl)propan-1-amine Organic Process Research and Development. 18: 904-911. DOI: 10.1021/Op5001513 |
0.52 |
|
| 2014 |
Cai Z, Liu G, Jiao G, Senanayake C, Tang W. ChemInform Abstract: Practical Syntheses of N-Acetyl (E)-β-Arylenamides. Cheminform. 45: no-no. DOI: 10.1002/chin.201423069 |
0.753 |
|
| 2014 |
Liu G, Xu G, Luo R, Tang W. ChemInform Abstract: Search for Ideal P-Chiral Phosphorus Ligands for Practical Asymmetric Hydrogenation and Asymmetric Suzuki-Miyaura Coupling Cheminform. 45: no-no. DOI: 10.1002/chin.201409259 |
0.801 |
|
| 2014 |
Tang W, Patel ND, Capacci AG, Wei X, Yee NK, Senanayake CH. Synthesis of N‐Acetyl Enamides by Reductive Acetylation of Oximes Mediated with Iron(II) Acetate: N‐(1‐(4‐Bromophenyl)vinyl)acetamide Organic Syntheses. 62-73. DOI: 10.1002/0471264229.Os090.06 |
0.303 |
|
| 2013 |
Luo R, Liao J, Xie L, Tang W, Chan AS. Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst. Chemical Communications (Cambridge, England). 49: 9959-61. PMID 24037423 DOI: 10.1039/C3Cc46009F |
0.486 |
|
| 2013 |
Li K, Hu N, Luo R, Yuan W, Tang W. A chiral ruthenium-monophosphine catalyst for asymmetric addition of arylboronic acids to aryl aldehydes. The Journal of Organic Chemistry. 78: 6350-5. PMID 23705850 DOI: 10.1021/Jo400850M |
0.519 |
|
| 2013 |
Liu G, Liu X, Cai Z, Jiao G, Xu G, Tang W. Design of phosphorus ligands with deep chiral pockets: practical synthesis of chiral β-arylamines by asymmetric hydrogenation. Angewandte Chemie (International Ed. in English). 52: 4235-8. PMID 23495148 DOI: 10.1002/Anie.201300646 |
0.806 |
|
| 2013 |
Zhao Q, Li C, Senanayake CH, Tang W. An efficient method for sterically demanding Suzuki-Miyaura coupling reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2261-5. PMID 23296637 DOI: 10.1002/Chem.201203898 |
0.699 |
|
| 2013 |
Tang W, Cai Z, Liu G, Jiao G, Senanayake C. Practical Syntheses of N-Acetyl (E)-β-Arylenamides Synthesis. 45: 3355-3360. DOI: 10.1055/S-0033-1339976 |
0.754 |
|
| 2013 |
Liu G, Xu G, Luo R, Tang W. Search for ideal P-chiral phosphorus ligands for practical asymmetric hydrogenation and asymmetric Suzuki-Miyaura coupling Synlett. 24: 2465-2471. DOI: 10.1055/S-0033-1339875 |
0.813 |
|
| 2013 |
Li W, Rodriguez S, Duran A, Sun X, Tang W, Premasiri A, Wang J, Sidhu K, Patel ND, Savoie J, Qu B, Lee H, Haddad N, Lorenz JC, Nummy L, et al. The P-chiral phosphane ligand (MeO-BIBOP) for efficient and practical large-scale Rh-catalyzed asymmetric hydrogenation of N-acetyl enamides with high TONs Organic Process Research and Development. 17: 1061-1065. DOI: 10.1021/Op400055Z |
0.447 |
|
| 2013 |
Tang W, Patel ND, Wei X, Byrne D, Chitroda A, Narayanan B, Sienkiewicz A, Nummy LJ, Sarvestani M, Ma S, Grinberg N, Lee H, Kim S, Li Z, Spinelli E, et al. Synthesis of a sodium-hydrogen exchange type 1 inhibitor: An efficient Cu-catalyzed conjugated addition of a Grignard reagent to an acetyl pyridinium salt Organic Process Research and Development. 17: 382-389. DOI: 10.1021/Op300331B |
0.477 |
|
| 2013 |
Luo R, Li K, Hu Y, Tang W. ChemInform Abstract: Enantioselective Rhodium-Catalyzed Addition of Arylboronic Acids to Trifluoromethyl Ketones. Cheminform. 44: no-no. DOI: 10.1002/chin.201338081 |
0.345 |
|
| 2013 |
Luo R, Li K, Hu Y, Tang W. Enantioselective rhodium-catalyzed addition of arylboronic acids to trifluoromethyl ketones Advanced Synthesis and Catalysis. 355: 1297-1302. DOI: 10.1002/Adsc.201201125 |
0.52 |
|
| 2012 |
Tang W, Patel ND, Xu G, Xu X, Savoie J, Ma S, Hao MH, Keshipeddy S, Capacci AG, Wei X, Zhang Y, Gao JJ, Li W, Rodriguez S, Lu BZ, et al. Efficient chiral monophosphorus ligands for asymmetric Suzuki-Miyaura coupling reactions. Organic Letters. 14: 2258-61. PMID 22497425 DOI: 10.1021/Ol300659D |
0.533 |
|
| 2011 |
Tang W, Keshipeddy S, Zhang Y, Wei X, Savoie J, Patel ND, Yee NK, Senanayake CH. Efficient monophosphorus ligands for palladium-catalyzed Miyaura borylation. Organic Letters. 13: 1366-9. PMID 21319836 DOI: 10.1021/Ol2000556 |
0.452 |
|
| 2011 |
Tang W, Wei X, Yee NK, Patel N, Lee H, Savoie J, Senanayake CH. A practical asymmetric synthesis of isopropyl (1 R,2 S)-dehydrocoronamate Organic Process Research and Development. 15: 1207-1211. DOI: 10.1021/Op200038Y |
0.377 |
|
| 2011 |
Li W, Gao JJ, Zhang Y, Tang W, Lee H, Fandrick KR, Lu B, Senanayake CH. A mild palladium-catalyzed Suzuki coupling reaction of quinoline carboxylates with boronic acids Advanced Synthesis and Catalysis. 353: 1671-1675. DOI: 10.1002/Adsc.201100141 |
0.436 |
|
| 2011 |
Rodriguez S, Qu B, Haddad N, Reeves DC, Tang W, Lee H, Krishnamurthy D, Senanayake CH. Oxaphosphole-based monophosphorus ligands for palladium-catalyzed amination reactions Advanced Synthesis and Catalysis. 353: 533-537. DOI: 10.1002/Adsc.201000878 |
0.484 |
|
| 2010 |
Tang W, Capacci AG, Wei X, Li W, White A, Patel ND, Savoie J, Gao JJ, Rodriguez S, Qu B, Haddad N, Lu BZ, Krishnamurthy D, Yee NK, Senanayake CH. A general and special catalyst for Suzuki-Miyaura coupling processes. Angewandte Chemie (International Ed. in English). 49: 5879-83. PMID 20632427 DOI: 10.1002/Anie.201002404 |
0.363 |
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| 2010 |
Fandrick DR, Fandrick KR, Reeves JT, Tan Z, Tang W, Capacci AG, Rodriguez S, Song JJ, Lee H, Yee NK, Senanayake CH. Copper catalyzed asymmetric propargylation of aldehydes. Journal of the American Chemical Society. 132: 7600-1. PMID 20481453 DOI: 10.1021/Ja103312X |
0.474 |
|
| 2010 |
Tang W, Capacci AG, White A, Ma S, Rodriguez S, Qu B, Savoie J, Patel ND, Wei X, Haddad N, Grinberg N, Yee NK, Krishnamurthy D, Senanayake CH. Novel and efficient chiral bisphosphorus ligands for rhodium-catalyzed asymmetric hydrogenation. Organic Letters. 12: 1104-7. PMID 20148522 DOI: 10.1021/Ol1000999 |
0.493 |
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| 2010 |
Tang W, Qu B, Capacci AG, Rodriguez S, Wei X, Haddad N, Narayanan B, Ma S, Grinberg N, Yee NK, Krishnamurthy D, Senanayake CH. Novel, tunable, and efficient chiral bisdihydrobenzooxaphosphole ligands for asymmetric hydrogenation. Organic Letters. 12: 176-9. PMID 19950894 DOI: 10.1021/Ol9025815 |
0.457 |
|
| 2010 |
Tang W, Capacci A, Wei X, Li W, White A, Patel N, Savoie J, Gao J, Rodriguez S, Qu B, Haddad N, Lu B, Krishnamurthy D, Yee N, Senanayake C. A Novel General Phosphine Ligand for Suzuki-Miyaura Cross-Coupling Synfacts. 2010: 1285-1285. DOI: 10.1055/S-0030-1258706 |
0.374 |
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| 2010 |
Fandrick DR, Fandrick KR, Reeves JT, Tan Z, Tang W, Capacci AG, Rodriguez S, Song JJ, Lee H, Yee NK, Senanayake CH. Enantioselective Propargylation of Aldehydes by Copper Catalysis Synfacts. 2010: 919-919. DOI: 10.1055/S-0030-1257775 |
0.389 |
|
| 2010 |
Tang W, Capacci AG, White A, Ma S, Rodriguez S, Qu B, Savoie J, Patel ND, Wei X, Haddad N, Grinberg N, Yee NK, Krishnamurthy D, Senanayake CH. Chiral Biphosphorous Ligands for Rhodium-Catalyzed AsymmetricHydrogenation Synfacts. 2010: 675-675. DOI: 10.1055/S-0029-1219978 |
0.477 |
|
| 2010 |
Zhou Y, Tang W, Wang W, Li W, Zhang X. ChemInform Abstract: Highly Effective Chiral ortho-Substituted BINAPO Ligands (o-BINAPO): Applications in Ru-Catalyzed Asymmetric Hydrogenations of β-Aryl-Substituted β-(Acylamino)acrylates and β-Keto Esters. Cheminform. 33: no-no. DOI: 10.1002/chin.200237031 |
0.571 |
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| 2009 |
Tang W, Capacci A, Sarvestani M, Wei X, Yee NK, Senanayake CH. A facile and practical synthesis of N-acetyl enamides. The Journal of Organic Chemistry. 74: 9528-30. PMID 19921804 DOI: 10.1021/Jo902259U |
0.406 |
|
| 2009 |
Ma S, Shen S, Haddad N, Tang W, Wang J, Lee H, Yee N, Senanayake C, Grinberg N. Chromatographic and spectroscopic studies on the chiral recognition of sulfated beta-cyclodextrin as chiral mobile phase additive enantiomeric separation of a chiral amine. Journal of Chromatography. A. 1216: 1232-40. PMID 19159891 DOI: 10.1016/J.Chroma.2008.12.016 |
0.303 |
|
| 2007 |
Han Z, Song JJ, Yee NK, Xu Y, Tang W, Reeves JT, Tan Z, Wang XJ, Lu B, Krishnamurthy D, Senanayake CH. Development of a preparative-scale asymmetric synthesis of (R)-p-tolyl methyl sulfoxide for use in a one-pot synthesis of a drug intermediate containing a trifluoromethyl-substituted alcohol functionality Organic Process Research and Development. 11: 605-608. DOI: 10.1021/Op700010A |
0.344 |
|
| 2006 |
Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Tang W, Frederick MO, Chen DY, Li Y, Ling T, Yamada YM. Total synthesis and structural elucidation of azaspiracid-1. Final assignment and total synthesis of the correct structure of azaspiracid-1. Journal of the American Chemical Society. 128: 2859-72. PMID 16506764 DOI: 10.1021/Ja054750Q |
0.739 |
|
| 2006 |
Nicolaou KC, Chen DY, Li Y, Uesaka N, Petrovic G, Koftis TV, Bernal F, Frederick MO, Govindasamy M, Ling T, Pihko PM, Tang W, Vyskocil S. Total synthesis and structural elucidation of azaspiracid-1. Synthesis-based analysis of originally proposed structures and indication of their non-identity to the natural product. Journal of the American Chemical Society. 128: 2258-67. PMID 16478179 DOI: 10.1021/Ja054748Z |
0.783 |
|
| 2006 |
Nicolaou K, Koftis T, Vyskocil S, Petrovic G, Tang W, Frederick M, Chen D, Ling T, Li Y, Yamada Y. Synthesis and Structural Elucidation of Azaspiracid-1 Synfacts. 2006: 0748-0748. DOI: 10.1055/S-2006-941937 |
0.734 |
|
| 2006 |
Ito E, Frederick MO, Koftis TV, Tang W, Petrovic G, Ling T, Nicolaou KC. Structure toxicity relationships of synthetic azaspiracid-1 and analogs in mice Harmful Algae. 5: 586-591. DOI: 10.1016/J.Hal.2005.11.005 |
0.505 |
|
| 2005 |
Nicolaou KC, Tang W, Dagneau P, Faraoni R. A catalytic asymmetric three-component 1,4-addition/aldol reaction: enantioselective synthesis of the spirocyclic system of vannusal A. Angewandte Chemie (International Ed. in English). 44: 3874-9. PMID 15900527 DOI: 10.1002/Anie.200500789 |
0.813 |
|
| 2005 |
Chi Y, Tang W, Zhang X. Rhodium-Catalyzed Asymmetric Hydrogenation Synfacts. 9: 1-31. DOI: 10.1002/3527604693.Ch1 |
0.6 |
|
| 2004 |
Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Ling T, Yamada YM, Tang W, Frederick MO. Structural revision and total synthesis of azaspiracid-1, part 2: definition of the ABCD domain and total synthesis. Angewandte Chemie (International Ed. in English). 43: 4318-24. PMID 15368381 DOI: 10.1002/Anie.200460696 |
0.689 |
|
| 2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YM, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Structural revision and total synthesis of azaspiracid-1, part 1: intelligence gathering and tentative proposal. Angewandte Chemie (International Ed. in English). 43: 4312-8. PMID 15368380 DOI: 10.1002/Anie.200460695 |
0.725 |
|
| 2004 |
Liu D, Tang W, Zhang X. Synthesis of a new class of conformationally rigid phosphino-oxazolines: highly enantioselective ligands for Ir-catalyzed asymmetric hydrogenation. Organic Letters. 6: 513-6. PMID 14961611 DOI: 10.1021/Ol0362717 |
0.725 |
|
| 2004 |
Nicolaou KC, Koftis TV, Vyskocil S, Petrovic G, Ling T, Yamada YMA, Tang W, Frederick MO. Structural Revision and Total Synthesis of Azaspiracid-1. Part 2. Definition of the ABCD Domain and Total Synthesis. Cheminform. 35. DOI: 10.1002/chin.200447211 |
0.526 |
|
| 2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Cover Picture: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. Int. Ed. 33/2004) Angewandte Chemie International Edition. 43: 4239-4239. DOI: 10.1002/Anie.200490111 |
0.646 |
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| 2004 |
Nicolaou KC, Vyskocil S, Koftis TV, Yamada YMA, Ling T, Chen DY, Tang W, Petrovic G, Frederick MO, Li Y, Satake M. Titelbild: Structural Revision and Total Synthesis of Azaspiracid-1, Part 1: Intelligence Gathering and Tentative Proposal (Angew. Chem. 33/2004) Angewandte Chemie. 116: 4335-4335. DOI: 10.1002/Ange.200490110 |
0.652 |
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| 2003 |
Tang W, Zhang X. New chiral phosphorus ligands for enantioselective hydrogenation. Chemical Reviews. 103: 3029-70. PMID 12914491 DOI: 10.1021/Cr020049I |
0.644 |
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| 2003 |
Tang W, Wu S, Zhang X. Enantioselective hydrogenation of tetrasubstituted olefins of cyclic beta-(acylamino)acrylates. Journal of the American Chemical Society. 125: 9570-1. PMID 12904006 DOI: 10.1021/Ja035777H |
0.64 |
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| 2003 |
Tang W, Wang W, Chi Y, Zhang X. A bisphosphepine ligand with stereogenic phosphorus centers for the practical synthesis of beta-aryl-beta-amino acids by asymmetric hydrogenation. Angewandte Chemie (International Ed. in English). 42: 3509-11. PMID 12900967 DOI: 10.1002/Anie.200351465 |
0.589 |
|
| 2003 |
Tang W, Wang W, Zhang X. Phospholane-oxazoline ligands for Ir-catalyzed asymmetric hydrogenation. Angewandte Chemie (International Ed. in English). 42: 943-6. PMID 12596185 DOI: 10.1002/Anie.200390251 |
0.621 |
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| 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 |
0.742 |
|
| 2003 |
Tang W, Liu D, Zhang X. Asymmetric hydrogenation of itaconic acid and enol acetate derivatives with the Rh-TangPhos catalyst. Organic Letters. 5: 205-7. PMID 12529141 DOI: 10.1021/Ol0272592 |
0.702 |
|
| 2002 |
Tang W, Zhang X. A chiral 1,2-bisphospholane ligand with a novel structural motif: applications in highly enantioselective Rh-catalyzed hydrogenations. Angewandte Chemie (International Ed. in English). 41: 1612-4. PMID 19750683 DOI: 10.1002/1521-3773(20020503)41:9<1612::Aid-Anie1612>3.0.Co;2-H |
0.668 |
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| 2002 |
Wu S, Wang W, Tang W, Lin M, Zhang X. Highly enantioselective hydrogenation of enol acetates catalyzed by Ru-TunaPhos complexes. Organic Letters. 4: 4495-7. PMID 12465921 DOI: 10.1021/Ol027010K |
0.642 |
|
| 2002 |
Tang W, Zhang X. Highly efficient synthesis of chiral beta-amino acid derivatives via asymmetric hydrogenation. Organic Letters. 4: 4159-61. PMID 12423111 DOI: 10.1021/Ol026935X |
0.608 |
|
| 2002 |
Tang W, Chi Y, Zhang X. An ortho-substituted BIPHEP ligand and its applications in Rh-catalyzed hydrogenation of cyclic enamides. Organic Letters. 4: 1695-8. PMID 12000276 DOI: 10.1021/Ol0258435 |
0.628 |
|
| 2002 |
Zhou YG, Tang W, Wang WB, Li W, Zhang X. Highly effective chiral ortho-substituted BINAPO ligands (o-BINAPO): applications in Ru-catalyzed asymmetric hydrogenations of beta-aryl-substituted beta-(acylamino)acrylates and beta-keto esters. Journal of the American Chemical Society. 124: 4952-3. PMID 11982347 DOI: 10.1021/Ja020121U |
0.656 |
|
| 2002 |
Körber K, Tang W, Hu X, Zhang X. A practical synthesis of 2-amino-2′-hydroxy-1,1′-binaphthyl (NOBIN) Tetrahedron Letters. 43: 7163-7165. DOI: 10.1016/S0040-4039(02)01674-X |
0.627 |
|
| 2002 |
Tang W, Hu X, Zhang X. A new chiral ruthenium complex for catalytic asymmetric cyclopropanation Tetrahedron Letters. 43: 3075-3078. DOI: 10.1016/S0040-4039(02)00317-9 |
0.64 |
|
| 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 |
0.547 |
|
| 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 |
0.545 |
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