Year |
Citation |
Score |
2022 |
Sarkar S, Banerjee A, Shah JA, Mukherjee U, Frederiks NC, Johnson CJ, Ngai MY. Excited-State Copper-Catalyzed [4 + 1] Annulation Reaction Enables Modular Synthesis of α,β-Unsaturated-γ-Lactams. Journal of the American Chemical Society. PMID 36326178 DOI: 10.1021/jacs.2c09006 |
0.304 |
|
2021 |
Zhao G, Yao W, Kevlishvili I, Mauro JN, Liu P, Ngai MY. Nickel-Catalyzed Radical Migratory Coupling Enables C-2 Arylation of Carbohydrates. Journal of the American Chemical Society. PMID 34086440 DOI: 10.1021/jacs.1c03563 |
0.392 |
|
2020 |
Lee JW, Lim S, Maienshein DN, Liu P, Ngai MY. Redox-Neutral TEMPO Catalysis Toward Direct Radical (Hetero)Aryl C-H Di- and Trifluoromethoxylation. Angewandte Chemie (International Ed. in English). PMID 32830430 DOI: 10.1002/Anie.202009490 |
0.438 |
|
2019 |
Sarkar S, Banerjee A, Yao W, Patterson EV, Ngai MY. Photocatalytic Radical Aroylation of Unactivated Alkenes: Pathway to β-Functionalized 1,4-, 1,6-, and 1,7-Diketones. Acs Catalysis. 9: 10358-10364. PMID 34040817 DOI: 10.1021/acscatal.9b03570 |
0.305 |
|
2019 |
Banerjee A, Lei Z, Ngai MY. Acyl Radical Chemistry via Visible-Light Photoredox Catalysis. Synthesis. 51: 303-333. PMID 31057188 DOI: 10.1055/S-0037-1610329 |
0.385 |
|
2019 |
Lee JW, Zheng W, Morales-Rivera CA, Liu P, Ngai MY. Catalytic radical difluoromethoxylation of arenes and heteroarenes. Chemical Science. 10: 3217-3222. PMID 30996904 DOI: 10.1039/C8Sc05390A |
0.457 |
|
2019 |
Lei Z, Banerjee A, Kusevska E, Rizzo E, Liu P, Ngai MY. β-Selective Aroylation of Activated Alkenes by Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 30994977 DOI: 10.1002/Anie.201901874 |
0.43 |
|
2019 |
Lee JW, Lee KN, Ngai MY. Synthesis of Tri- and Difluoromethoxylated Compounds via Visible Light Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 30943329 DOI: 10.1002/Anie.201902243 |
0.34 |
|
2018 |
Lee KN, Lee JW, Ngai MY. Recent Development of Catalytic Trifluoromethoxylation Reactions. Tetrahedron. 74: 7127-7135. PMID 30906076 DOI: 10.1016/J.Tet.2018.09.020 |
0.381 |
|
2018 |
Zheng W, Lee JW, Morales-Rivera CA, Liu P, Ngai MY. Redox-Active Reagents for Photocatalytic Generation of the OCF Radical and (Hetero)Aryl C-H Trifluoromethoxylation. Angewandte Chemie (International Ed. in English). PMID 30238593 DOI: 10.1002/Anie.201808495 |
0.395 |
|
2018 |
Zheng W, Morales-Rivera CA, Lee JW, Liu P, Ngai MY. Catalytic C-H Trifluoromethoxylation of Arenes and Heteroarenes. Angewandte Chemie (International Ed. in English). PMID 29534322 DOI: 10.1002/Anie.201800598 |
0.462 |
|
2017 |
Lee KN, Ngai MY. Recent developments in transition-metal photoredox-catalysed reactions of carbonyl derivatives. Chemical Communications (Cambridge, England). PMID 29125152 DOI: 10.1039/C7Cc06287G |
0.411 |
|
2017 |
Lee JW, Spiegowski DN, Ngai MY. Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenes. Chemical Science. 8: 6066-6070. PMID 28989637 DOI: 10.1039/C7Sc01684K |
0.448 |
|
2017 |
Lee KN, Lei Z, Ngai MY. β-Selective Reductive Coupling of Alkenylpyridines with Aldehydes and Imines via Synergistic Lewis Acid/Photoredox Catalysis. Journal of the American Chemical Society. PMID 28358497 DOI: 10.1021/Jacs.7B01373 |
0.462 |
|
2016 |
Lee KN, Lee JW, Ngai MY. Synthesis of Trifluoromethoxylated (Hetero)Arenes via OCF3 Migration. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 27: 313-319. PMID 27872511 DOI: 10.1055/S-0035-1560516 |
0.399 |
|
2016 |
Feng P, Lee KN, Lee JW, Zhan C, Ngai MY. Access to a new class of synthetic building blocks via trifluoromethoxylation of pyridines and pyrimidines. Chemical Science. 7: 424-429. PMID 27857834 DOI: 10.1039/C5Sc02983J |
0.382 |
|
2016 |
Lee KN, Lei Z, Morales-Rivera CA, Liu P, Ngai MY. Mechanistic studies on intramolecular C-H trifluoromethoxylation of (hetero)arenes via OCF3-migration. Organic & Biomolecular Chemistry. PMID 27043815 DOI: 10.1039/C6Ob00132G |
0.398 |
|
2016 |
Feng P, Ngai MY. Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives. Journal of Visualized Experiments : Jove. PMID 26862864 DOI: 10.3791/53789 |
0.42 |
|
2015 |
Trost BM, Biannic B, Brindle CS, O'Keefe BM, Hunter TJ, Ngai MY. A Highly Convergent Total Synthesis of Leustroducsin B. Journal of the American Chemical Society. 137: 11594-7. PMID 26313159 DOI: 10.1021/Jacs.5B07438 |
0.725 |
|
2014 |
Hojczyk KN, Feng P, Zhan C, Ngai MY. Trifluoromethoxylation of arenes: synthesis of ortho-trifluoromethoxylated aniline derivatives by OCF3 migration. Angewandte Chemie (International Ed. in English). 53: 14559-63. PMID 25358501 DOI: 10.1002/Ange.201409375 |
0.433 |
|
2013 |
Boursalian GB, Ngai MY, Hojczyk KN, Ritter T. Pd-catalyzed aryl C-H imidation with arene as the limiting reagent. Journal of the American Chemical Society. 135: 13278-81. PMID 23998528 DOI: 10.1021/Ja4064926 |
0.609 |
|
2011 |
Trost BM, Ngai MY, Dong G. Ligand-accelerated enantioselective propargylation of aldehydes via allenylzinc reagents. Organic Letters. 13: 1900-3. PMID 21391717 DOI: 10.1021/Ol200043N |
0.639 |
|
2011 |
Trost BM, Ngai M, Dong G. ChemInform Abstract: Ligand-Accelerated Enantioselective Propargylation of Aldehydes via Allenylzinc Reagents. Cheminform. 42: no-no. DOI: 10.1002/chin.201130065 |
0.463 |
|
2009 |
Liechti KM, Wakamatsu M, Doynov B, Ngai MY, Krische MJ. Fracture between self-assembled monolayers Iccm International Conferences On Composite Materials. |
0.489 |
|
2008 |
Kim IS, Ngai MY, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition. Journal of the American Chemical Society. 130: 14891-9. PMID 18841896 DOI: 10.1021/Ja805722E |
0.694 |
|
2008 |
Ngai MY, Skucas E, Krische MJ. Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes. Organic Letters. 10: 2705-8. PMID 18533665 DOI: 10.1021/Ol800836V |
0.682 |
|
2008 |
Kim IS, Ngai MY, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate. Journal of the American Chemical Society. 130: 6340-1. PMID 18444616 DOI: 10.1021/Ja802001B |
0.699 |
|
2007 |
Ngai MY, Barchuk A, Krische MJ. Enantioselective iridium-catalyzed imine vinylation: optically enriched allylic amines via alkyne-imine reductive coupling mediated by hydrogen. Journal of the American Chemical Society. 129: 12644-5. PMID 17914825 DOI: 10.1021/Ja075438E |
0.713 |
|
2007 |
Skucas E, Ngai MY, Komanduri V, Krische MJ. Enantiomerically enriched allylic alcohols and allylic amines via C-C bond-forming hydrogenation: asymmetric carbonyl and imine vinylation. Accounts of Chemical Research. 40: 1394-401. PMID 17784728 DOI: 10.1021/Ar7001123 |
0.67 |
|
2007 |
Barchuk A, Ngai MY, Krische MJ. Allylic amines via iridium-catalyzed C-C bond forming hydrogenation: imine vinylation in the absence of stoichiometric byproducts or metallic reagents. Journal of the American Chemical Society. 129: 8432-3. PMID 17571894 DOI: 10.1021/Ja073018J |
0.677 |
|
2007 |
Ngai MY, Kong JR, Krische MJ. Hydrogen-mediated C-C bond formation: a broad new concept in catalytic C-C coupling. The Journal of Organic Chemistry. 72: 1063-72. PMID 17288361 DOI: 10.1021/Jo061895M |
0.677 |
|
2007 |
Ngai MY, Barchuk A, Krische MJ. Iridium-catalyzed C-C bond forming hydrogenation: direct regioselective reductive coupling of alkyl-substituted alkynes to activated ketones. Journal of the American Chemical Society. 129: 280-1. PMID 17212400 DOI: 10.1021/Ja0670815 |
0.716 |
|
2006 |
Kong JR, Ngai MY, Krische MJ. Highly enantioselective direct reductive coupling of conjugated alkynes and alpha-ketoesters via rhodium-catalyzed asymmetric hydrogenation. Journal of the American Chemical Society. 128: 718-9. PMID 16417351 DOI: 10.1021/Ja056474L |
0.739 |
|
2006 |
Kong J, Ngai M, Krische MJ. Enantioselective Direct Reductive Coupling of Conjugated Alkynes and α-Ketoesters Synfacts. 2006: 359-359. DOI: 10.1055/S-2006-934337 |
0.648 |
|
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