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Chau-Ming So, Ph.D. - Publications

Affiliations: 
2010 Hong Kong Polytechnic University (Hong Kong) 
Area:
Organic Chemistry
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39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Wang M, Pang WH, Yuen OY, Ng SS, So CM. Palladium-Catalyzed Deuterodehalogenation of Halogenated Aryl Triflates Using Isopropanol- as the Deuterium Source. Organic Letters. PMID 37975627 DOI: 10.1021/acs.orglett.3c03281  0.399
2022 Chen Z, Gu C, Yuen OY, So CM. Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C-Cl site. Chemical Science. 13: 4762-4769. PMID 35655875 DOI: 10.1039/d1sc06701j  0.456
2022 Ng SS, Chen Z, Yuen OY, So CM. An indole-amide-based phosphine ligand enabling a general palladium-catalyzed sterically hindered Suzuki-Miyaura cross-coupling reaction. Organic & Biomolecular Chemistry. PMID 35080549 DOI: 10.1039/d1ob02294f  0.534
2022 Wang M, So CM. Inverting Conventional Chemoselectivity in the Sonogashira Coupling Reaction of Polyhalogenated Aryl Triflates with TMS-Arylalkynes. Organic Letters. 24: 681-685. PMID 34978819 DOI: 10.1021/acs.orglett.1c04138  0.518
2020 Yuen OY, So CM. A Ligand Control of Palladium-Catalyzed Site-Selective α- and γ-Arylation of α,β-Unsaturated Ketones with (Hetero)aryl Halides. Angewandte Chemie (International Ed. in English). PMID 33007134 DOI: 10.1002/anie.202010682  0.425
2020 Chen Z, So CM. Pd-Catalyzed Cross-Coupling of Highly Sterically Congested Enol Carbamates with Grignard Reagents via C-O Bond Activation. Organic Letters. PMID 32352793 DOI: 10.1021/acs.orglett.0c01127  0.527
2019 Chen X, Chen Z, So CM. Exploration of Aryl Phosphates in Palladium-Catalyzed Mono-α-arylation of Aryl and Heteroaryl Ketones. The Journal of Organic Chemistry. PMID 31045364 DOI: 10.1021/acs.joc.9b00669  0.609
2019 Chen Z, Chen X, So CM. Palladium-Catalyzed C(sp)-N Bond Cross-Coupling with Triaryl Phosphates. The Journal of Organic Chemistry. PMID 31038958 DOI: 10.1021/acs.joc.9b00703  0.532
2018 Yang Q, Choy PY, Zhao Q, Leung MP, Chan HS, So CM, Wong WT, Kwong FY. Palladium-Catalyzed N-Arylation of Sulfoximines with Aryl Sulfonates. The Journal of Organic Chemistry. PMID 30062889 DOI: 10.1021/Acs.Joc.8B01599  0.534
2018 Yuen OY, Leung MP, So CM, Sun RW, Kwong FY. Palladium-Catalyzed Direct Arylation of Polyfluoroarenes for Accessing Tetra-ortho-Substituted Biaryls: Buchwald-type Ligand Having Complementary -PPh2 Moiety Exhibits Better Efficiency. The Journal of Organic Chemistry. PMID 29882668 DOI: 10.1021/Acs.Joc.8B01176  0.584
2018 Choy PY, Chung KH, Yang Q, So CM, Sun RW, Kwong FY. A General Palladium-Phosphine Complex for Exploring Aryl Tosylates in N-arylation of Amines: Scope and Limitation. Chemistry, An Asian Journal. PMID 29742319 DOI: 10.1002/Asia.201800575  0.622
2016 Fu WC, Wu Y, So CM, Wong SM, Lei A, Kwong FY. Catalytic Direct C2-Alkenylation of Oxazoles at Parts per Million Levels of Palladium/PhMezole-Phos Complex. Organic Letters. PMID 27726381 DOI: 10.1021/Acs.Orglett.6B02619  0.477
2016 Fu WC, So CM, Yuen OY, Lee IT, Kwong FY. Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones. Organic Letters. PMID 27046738 DOI: 10.1021/Acs.Orglett.6B00643  0.57
2016 Yuen OY, So CM, Man HW, Kwong FY. A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26998586 DOI: 10.1002/Chem.201600420  0.568
2016 Kwong F, Kantchev E, Li Y, Wang Z, Zou Y, So C, Qin H. Bulky Phosphane Ligand for Monoselective Ruthenium-Catalyzed, Directed o-C–H Arylation with Challenging Aryl Chlorides Synlett. 28: 499-503. DOI: 10.1055/S-0036-1588635  0.404
2015 Fu WC, So CM, Kwong FY. Palladium-Catalyzed Phosphorylation of Aryl Mesylates and Tosylates. Organic Letters. PMID 26574778 DOI: 10.1021/Acs.Orglett.5B03104  0.451
2015 Fu WC, So CM, Chow WK, Yuen OY, Kwong FY. Design of an Indolylphosphine Ligand for Reductive Elimination-Demanding Monoarylation of Acetone Using Aryl Chlorides. Organic Letters. 17: 4612-5. PMID 26352174 DOI: 10.1021/Acs.Orglett.5B02344  0.505
2015 Yuen OY, Charoensak M, So CM, Kuhakarn C, Kwong FY. A general direct arylation of polyfluoroarenes with heteroaryl and aryl chlorides catalyzed by palladium indolylphosphine complexes. Chemistry, An Asian Journal. 10: 857-61. PMID 25678211 DOI: 10.1002/Asia.201500048  0.547
2015 Choy PY, Luk KC, Wu Y, So CM, Wang LL, Kwong FY. Regioselective direct C-3 arylation of imidazo[1,2-a]pyridines with aryl tosylates and mesylates promoted by palladium-phosphine complexes. The Journal of Organic Chemistry. 80: 1457-63. PMID 25607730 DOI: 10.1021/Jo502386W  0.502
2015 He Q, So CM, Bian Z, Hayashi T, Wang J. Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to chromones: a highly enantioselective pathway for accessing chiral flavanones. Chemistry, An Asian Journal. 10: 540-3. PMID 25585883 DOI: 10.1002/Asia.201403290  0.419
2015 Fu WC, So CM, Chow WK, Yuen OY, Kwong FY. Design of an Indolylphosphine Ligand for Reductive Elimination-Demanding Monoarylation of Acetone Using Aryl Chlorides Organic Letters. 17: 4612-4615. DOI: 10.1021/acs.orglett.5b02344  0.329
2013 So CM, Kume S, Hayashi T. Rhodium-catalyzed asymmetric hydroarylation of 3-pyrrolines giving 3-arylpyrrolidines: protonation as a key step. Journal of the American Chemical Society. 135: 10990-3. PMID 23865491 DOI: 10.1021/Ja406169S  0.377
2012 Chow WK, Yuen OY, So CM, Wong WT, Kwong FY. Carbon-boron bond cross-coupling reaction catalyzed by -PPh(2) containing palladium-indolylphosphine complexes. The Journal of Organic Chemistry. 77: 3543-8. PMID 22414161 DOI: 10.1021/Jo202472K  0.637
2012 Chung KH, So CM, Wong SM, Luk CH, Zhou Z, Lau CP, Kwong FY. An efficient palladium-benzimidazolyl phosphine complex for the Suzuki-Miyaura coupling of aryl mesylates: facile ligand synthesis and metal complex characterization. Chemical Communications (Cambridge, England). 48: 1967-9. PMID 22234641 DOI: 10.1039/C2Cc15972D  0.55
2011 So CM, Kwong FY. Palladium-catalyzed cross-coupling reactions of aryl mesylates. Chemical Society Reviews. 40: 4963-72. PMID 21858311 DOI: 10.1039/C1Cs15114B  0.512
2011 Wong PY, Chow WK, Chung KH, So CM, Lau CP, Kwong FY. A versatile palladium catalyst system for Suzuki-Miyaura coupling of alkenyl tosylates and mesylates. Chemical Communications (Cambridge, England). 47: 8328-30. PMID 21681318 DOI: 10.1039/C1Cc12240A  0.567
2011 Chow WK, So CM, Lau CP, Kwong FY. Palladium-catalyzed borylation of aryl mesylates and tosylates and their applications in one-pot sequential Suzuki-Miyaura biaryl synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6913-7. PMID 21547969 DOI: 10.1002/Chem.201100361  0.533
2011 So CM, Lau CP, Kwong FY. Palladium-catalyzed direct arylation of heteroarenes with aryl mesylates. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 761-5. PMID 21226087 DOI: 10.1002/Chem.201002354  0.613
2011 Yeung PY, So CM, Lau CP, Kwong FY. A mild and efficient palladium-catalyzed cyanation of aryl chlorides with K4[Fe(CN)6]. Organic Letters. 13: 648-51. PMID 21208008 DOI: 10.1021/Ol1028892  0.577
2010 Choy PY, Chow WK, So CM, Lau CP, Kwong FY. Palladium-catalyzed sonogashira coupling of aryl mesylates and tosylates. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9982-5. PMID 20665584 DOI: 10.1002/Chem.201001269  0.558
2010 Chow WK, So CM, Lau CP, Kwong FY. A general palladium catalyst system for Suzuki-Miyaura coupling of potassium aryltrifluoroborates and aryl mesylates. The Journal of Organic Chemistry. 75: 5109-12. PMID 20590104 DOI: 10.1021/Jo100846T  0.571
2010 So CM, Chow WK, Choy PY, Lau CP, Kwong FY. Remarkably effective phosphanes simply with a PPh2 moiety: application to Pd-catalysed cross-coupling reactions for tetra-ortho-substituted biaryl syntheses. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 7996-8001. PMID 20564295 DOI: 10.1002/Chem.201000723  0.466
2009 Lee HW, Lam FL, So CM, Lau CP, Chan AS, Kwong FY. Palladium-catalyzed cross-coupling of aryl halides using organotitanium nucleophiles. Angewandte Chemie (International Ed. in English). 48: 7436-9. PMID 19731296 DOI: 10.1002/Anie.200904033  0.522
2009 So CM, Lee HW, Lau CP, Kwong FY. Palladium-indolylphosphine-catalyzed Hiyama cross-coupling of aryl mesylates. Organic Letters. 11: 317-20. PMID 19099495 DOI: 10.1021/Ol802493Z  0.601
2008 So CM, Lau CP, Kwong FY. A general palladium-catalyzed Suzuki-Miyaura coupling of aryl mesylates. Angewandte Chemie (International Ed. in English). 47: 8059-63. PMID 18785669 DOI: 10.1002/Anie.200803193  0.545
2008 So CM, Lau CP, Chan AS, Kwong FY. Suzuki-Miyaura coupling of aryl tosylates catalyzed by an array of indolyl phosphine-palladium catalysts. The Journal of Organic Chemistry. 73: 7731-4. PMID 18783275 DOI: 10.1021/Jo8014819  0.578
2008 So CM, Yeung CC, Lau CP, Kwong FY. A new family of tunable indolylphosphine ligands by one-pot assembly and their applications in Suzuki-Miyaura coupling of aryl chlorides. The Journal of Organic Chemistry. 73: 7803-6. PMID 18778101 DOI: 10.1021/Jo801544W  0.526
2008 So CM, Zhou Z, Lau CP, Kwong FY. Palladium-catalyzed amination of aryl mesylates. Angewandte Chemie (International Ed. in English). 47: 6402-6. PMID 18618887 DOI: 10.1002/Anie.200802157  0.62
2007 So CM, Lau CP, Kwong FY. Easily accessible and highly tunable indolyl phosphine ligands for Suzuki-Miyaura coupling of aryl chlorides. Organic Letters. 9: 2795-8. PMID 17602563 DOI: 10.1021/Ol070898Y  0.564
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