Liangbin Huang - Publications

Affiliations: 
University of Rochester, Rochester, NY 

66 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
2024 Jia X, Xing D, Shen J, Li B, Zeng Y, Jiang H, Huang L. 1,2,3-Thiadiazole as a Modifiable and Scalable Directing Group for -C-H Functionalization. Organic Letters. PMID 38358975 DOI: 10.1021/acs.orglett.3c04075  0.339
2024 Zhang J, Zhu W, Xiao D, Zhou P, Huang L, Liu W. TBHP Mediated C-N Bond Cleavage of Tertiary Amines toward the Synthesis of Oxalamides and α,β-Epoxy Amides. The Journal of Organic Chemistry. PMID 38207216 DOI: 10.1021/acs.joc.3c02119  0.378
2023 Li B, Xing D, Li X, Chang S, Jiang H, Huang L. Chemo-divergent Cyano Group Migration: Involving Elimination and Substitution of the Key α-Thianthrenium Cyano Species. Organic Letters. PMID 37672391 DOI: 10.1021/acs.orglett.3c02396  0.337
2023 Chang S, Xing D, Zheng Y, Huang L. Copper-Catalyzed Synthesis of Quinoline-4-thiols from Diaryliodonium Salts, Alkynyl Sulfides, and Nitriles. Organic Letters. PMID 37439531 DOI: 10.1021/acs.orglett.3c01929  0.376
2022 Liu J, Jia X, Huang L. Sulfilimines as Transformable and Retainable Directing Groups in Rhodium-Catalyzed -C-H Bond Functionalization. Organic Letters. 24: 6772-6776. PMID 36098745 DOI: 10.1021/acs.orglett.2c02630  0.389
2022 Su Y, Li B, Xu H, Lu C, Wang S, Chen B, Wang Z, Wang W, Otake KI, Kitagawa S, Huang L, Gu C. Multi-Component Synthesis of a Buta-1,3-diene-Linked Covalent Organic Framework. Journal of the American Chemical Society. PMID 36069433 DOI: 10.1021/jacs.2c05701  0.34
2022 Yang Y, Huang L, Jiang K, Cao X, Yin B. LiCl-Mediated and Palladium-Catalyzed Oxidative Cyclization of Furan-Ynes via Dearomatizing Alkoxyalkenylation of Furan. Organic Letters. PMID 35451840 DOI: 10.1021/acs.orglett.2c01157  0.443
2022 Liu J, Lin H, Jiang H, Huang L. Polysubstituted Indole Synthesis via Palladium/Norbornene Cooperative Catalysis of Oxime Esters. Organic Letters. PMID 34978457 DOI: 10.1021/acs.orglett.1c03679  0.488
2021 Lin Z, Huang L, Yuan G. Electrosynthesis of sulfonamides from DMSO and amines under mild conditions. Chemical Communications (Cambridge, England). PMID 33709092 DOI: 10.1039/d1cc00026h  0.324
2020 Su Y, Wan Y, Xu H, Otake KI, Tang X, Huang L, Kitagawa S, Gu C. Crystalline and Stable Benzofuran-Linked Covalent Organic Frameworks from Irreversible Cascade Reactions. Journal of the American Chemical Society. PMID 32674574 DOI: 10.1021/Jacs.0C05970  0.492
2020 Kang K, Huang L, Weix DJ. Sulfonate vs Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates. Journal of the American Chemical Society. PMID 32486635 DOI: 10.1021/Jacs.0C04670  0.689
2019 He D, Huang L, Li J, Wu W, Jiang H. Palladium-Catalyzed Nitrile-Assisted C(sp)-Cl Bond Formation for Synthesis of Dichlorides. Organic Letters. PMID 31566389 DOI: 10.1021/Acs.Orglett.9B03066  0.551
2019 Huang L, Ackerman LKG, Kang K, Parsons AM, Weix DJ. LiCl Accelerated Multimetallic Cross-Coupling of Aryl Chlorides with Aryl Triflates. Journal of the American Chemical Society. PMID 31257881 DOI: 10.1021/Jacs.9B05461  0.702
2019 Cen J, Wu Y, Li J, Huang L, Wu W, Zhu Z, Yang S, Jiang H. Switchable Reactivity between Vinyl Azides and Terminal Alkyne by Nano Copper Catalysis. Organic Letters. PMID 30869904 DOI: 10.1021/Acs.Orglett.9B00373  0.517
2019 Liang E, Wang J, Wu Y, Huang L, Yao X, Tang X. Direct Alkenylation of 2‐Methylquinolines with Aldehydes through Synergistic Catalysis of 1,3‐Dimethylbarbituric Acid and HOAc Advanced Synthesis & Catalysis. 361: 3619-3623. DOI: 10.1002/Adsc.201900351  0.373
2017 Zheng M, Chen P, Huang L, Wu W, Jiang H. Nucleo-Palladation-Triggering Alkene Functionalization: A Route to γ-Lactones. Organic Letters. PMID 29072076 DOI: 10.1021/Acs.Orglett.7B02688  0.466
2017 Huang L, Olivares AM, Weix DJ. Reductive Decarboxylative Alkynylation of N-Hydroxyphthalimide Esters with Bromoalkynes. Angewandte Chemie (International Ed. in English). PMID 28782860 DOI: 10.1002/Anie.201706781  0.676
2016 Huang L, Weix DJ. Ruthenium-Catalyzed C-H Arylation of Diverse Aryl Carboxylic Acids with Aryl and Heteroaryl Halides. Organic Letters. PMID 27736085 DOI: 10.1021/Acs.Orglett.6B02862  0.719
2016 Zheng J, Li Z, Huang L, Wu W, Li J, Jiang H. Palladium-Catalyzed Intermolecular Aerobic Annulation of o-Alkenylanilines and Alkynes for Quinoline Synthesis. Organic Letters. PMID 27418021 DOI: 10.1021/Acs.Orglett.6B01008  0.485
2016 Huang L, Biafora A, Zhang G, Bragoni V, Gooßen LJ. Regioselective C-H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups. Angewandte Chemie (International Ed. in English). PMID 27112925 DOI: 10.1002/Anie.201600894  0.535
2016 Zheng M, Huang L, Tong Q, Wu W, Jiang H. Oxypalladation Initiating the Oxid-ative Heck Reaction with Alkenyl -Alcohols: Synthesis of Isocoumarin-Alkanones European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201501451  0.52
2016 Zheng M, Huang L, Tong Q, Wu W, Jiang H. ChemInform Abstract: Oxypalladation Initiating the Oxidative Heck Reaction with Alkenyl Alcohols: Synthesis of Isocoumarin-Alkanones. Cheminform. 47. DOI: 10.1002/CHIN.201625154  0.358
2015 Huang L, Hackenberger D, Gooßen LJ. Iridium-Catalyzed ortho-Arylation of Benzoic Acids with Arenediazonium Salts. Angewandte Chemie (International Ed. in English). 54: 12607-11. PMID 26465654 DOI: 10.1002/Anie.201505769  0.515
2015 Zheng J, Huang L, Li Z, Wu W, Li J, Jiang H. Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines. Chemical Communications (Cambridge, England). 51: 5894-7. PMID 25729782 DOI: 10.1039/C4Cc10322J  0.492
2015 Zheng J, Huang L, Huang C, Wu W, Jiang H. Synthesis of polysubstituted pyrroles via Pd-catalyzed oxidative alkene C-H bond arylation and amination. The Journal of Organic Chemistry. 80: 1235-42. PMID 25536027 DOI: 10.1021/Jo502414W  0.534
2014 Zheng M, Huang L, Huang H, Li X, Wu W, Jiang H. Palladium-catalyzed sequential C-N/C-O bond formations: synthesis of oxazole derivatives from amides and ketones. Organic Letters. 16: 5906-9. PMID 25393588 DOI: 10.1021/Ol502916A  0.518
2014 Tang X, Huang L, Yang J, Xu Y, Wu W, Jiang H. Practical synthesis of pyrazoles via a copper-catalyzed relay oxidation strategy. Chemical Communications (Cambridge, England). 50: 14793-6. PMID 25319768 DOI: 10.1039/C4Cc06747A  0.534
2014 Huang L, Wang Q, Wu W, Jiang H. Nucleopalladation-initiated oxyalkenylation of alkenes: a strategy to construct functionalized oxygenated heterocycles. The Journal of Organic Chemistry. 79: 7734-9. PMID 25023743 DOI: 10.1021/Jo501317V  0.508
2014 Li J, Yang W, Yang S, Huang L, Wu W, Sun Y, Jiang H. Palladium-catalyzed cascade annulation to construct functionalized β- and γ-lactones in ionic liquids. Angewandte Chemie (International Ed. in English). 53: 7219-22. PMID 24866483 DOI: 10.1002/Anie.201403341  0.449
2014 Tang X, Huang L, Xu Y, Yang J, Wu W, Jiang H. Copper-catalyzed coupling of oxime acetates with sodium sulfinates: an efficient synthesis of sulfone derivatives. Angewandte Chemie (International Ed. in English). 53: 4205-8. PMID 24677481 DOI: 10.1002/Anie.201311217  0.615
2014 Yu Y, Huang L, Wu W, Jiang H. Palladium-catalyzed oxidative annulation of acrylic acid and amide with alkynes: a practical route to synthesize α-pyrones and pyridones. Organic Letters. 16: 2146-9. PMID 24673501 DOI: 10.1021/Ol500611D  0.507
2014 Zheng J, Zhang M, Huang L, Hu X, Wu W, Huang H, Jiang H. Regioselective synthesis of oxazole derivatives via palladium-catalyzed and copper-mediated cascade oxidative cyclization. Chemical Communications (Cambridge, England). 50: 3609-11. PMID 24572568 DOI: 10.1039/C3Cc49788G  0.501
2014 Huang L, Wang Q, Wu W, Jiang H. ChemInform Abstract: Palladium/Copper Bimetallic System-Mediated Cross-Coupling of Alkynes and Alkenes: Two Strategies to Suppress β-H Elimination on Alkyl-Palladium Center. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201449064  0.434
2014 Huang L, Wang Q, Wu W, Jiang H. Hydroxyl Group-Assisted Palladium-Catalyzed Lactonization of Homoallylic Alcohols Chemcatchem. 6: 561-566. DOI: 10.1002/Cctc.201300903  0.462
2014 Tang X, Huang L, Xu Y, Yang J, Wu W, Jiang H. Inside Cover: Copper-Catalyzed Coupling of Oxime Acetates with Sodium Sulfinates: An Efficient Synthesis of Sulfone Derivatives (Angew. Chem. Int. Ed. 16/2014) Angewandte Chemie International Edition. 53: 4010-4010. DOI: 10.1002/Anie.201401135  0.527
2014 Tang X, Huang L, Xu Y, Yang J, Wu W, Jiang H. Innentitelbild: Copper-Catalyzed Coupling of Oxime Acetates with Sodium Sulfinates: An Efficient Synthesis of Sulfone Derivatives (Angew. Chem. 16/2014) Angewandte Chemie. 126: 4090-4090. DOI: 10.1002/Ange.201401135  0.535
2014 Huang L, Wang Q, Wu W, Jiang H. Palladium/Copper Bimetallic System-Mediated Cross-Coupling of Alkynes and Alkenes: Two Strategies to Suppress β-H Elimination on Alkyl-Palladium Center Advanced Synthesis & Catalysis. 356: 1949-1954. DOI: 10.1002/Adsc.201400007  0.515
2013 Wang Q, Huang L, Wu X, Jiang H. Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Organic Letters. 15: 5940-3. PMID 24237319 DOI: 10.1021/Ol4027683  0.486
2013 Huang L, Qi J, Wu X, Wu W, Jiang H. Aerobic oxidative coupling between carbon nucleophiles and allylic alcohols: a strategy to construct β-(hetero)aryl ketones and aldehydes through hydrogen migration. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 15462-6. PMID 24151227 DOI: 10.1002/Chem.201302962  0.562
2013 Qi J, Huang L, Wang Z, Jiang H. Ruthenium- and rhodium-catalyzed oxidative alkylation of C-H bonds: efficient access to β-aryl ketones. Organic & Biomolecular Chemistry. 11: 8009-13. PMID 24057305 DOI: 10.1039/C3Ob41590B  0.601
2013 Tang X, Huang L, Qi C, Wu W, Jiang H. An efficient synthesis of polysubstituted pyrroles via copper-catalyzed coupling of oxime acetates with dialkyl acetylenedicarboxylates under aerobic conditions. Chemical Communications (Cambridge, England). 49: 9597-9. PMID 24018713 DOI: 10.1039/C3Cc44896G  0.544
2013 Zeng W, Wu W, Jiang H, Huang L, Sun Y, Chen Z, Li X. Facile synthesis of benzofurans via copper-catalyzed aerobic oxidative cyclization of phenols and alkynes. Chemical Communications (Cambridge, England). 49: 6611-3. PMID 23772445 DOI: 10.1039/C3Cc42326C  0.511
2013 Tang X, Huang L, Qi C, Wu X, Wu W, Jiang H. Copper-catalyzed sulfonamides formation from sodium sulfinates and amines. Chemical Communications (Cambridge, England). 49: 6102-4. PMID 23730689 DOI: 10.1039/C3Cc41249K  0.528
2013 Huang L, Qi J, Wu X, Huang K, Jiang H. Highly selective β-hydride elimination in Pd-catalyzed decarboxylative Heck-type reaction. Organic Letters. 15: 2330-3. PMID 23621714 DOI: 10.1021/Ol400818V  0.496
2013 Zheng M, Huang L, Wu W, Jiang H. Pd(II)-catalyzed sequential C-C/C-O bond formations: a new strategy to construct trisubstituted furans. Organic Letters. 15: 1838-41. PMID 23540567 DOI: 10.1021/Ol400451T  0.475
2013 Huang H, Ji X, Wu W, Huang L, Jiang H. Copper-catalyzed formal C-N bond cleavage of aromatic methylamines: Assembly of pyridine derivatives Journal of Organic Chemistry. 78: 3774-3782. PMID 23496336 DOI: 10.1021/Jo400261V  0.531
2013 Huang L, Wang Q, Qi J, Wu X, Huang K, Jiang H. Rh(iii)-catalyzed ortho-oxidative alkylation of unactivated arenes with allylic alcohols Chemical Science. 4: 2665. DOI: 10.1039/C3Sc50630D  0.564
2013 Li J, Yang S, Huang L, Chen H, Jiang H. Highly efficient and practical synthesis of functionalized 1,5-dienes via Pd(ii)-catalyzed halohomoallylation of alkynes Rsc Advances. 3: 11529. DOI: 10.1039/C3Ra41690A  0.496
2013 Huang L, Wang Q, Qi J, Wu X, Huang K, Jiang H. ChemInform Abstract: Rh(III)-Catalyzed ortho-Oxidative Alkylation of Unactivated Arenes with Allylic Alcohols. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201346057  0.331
2013 Li X, Huang L, Chen H, Wu W, Huang H, Jiang H. ChemInform Abstract: Copper-Catalyzed Oxidative [2 + 2 + 1] Cycloaddition: Regioselective Synthesis of 1,3-Oxazoles from Internal Alkynes and Nitriles. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201317119  0.426
2012 Yuan G, Zheng J, Gao X, Li X, Huang L, Chen H, Jiang H. Copper-catalyzed aerobic oxidation and cleavage/formation of C-S bond: a novel synthesis of aryl methyl sulfones from aryl halides and DMSO. Chemical Communications (Cambridge, England). 48: 7513-5. PMID 22728918 DOI: 10.1039/C2Cc32964F  0.557
2012 Wen Y, Huang L, Jiang H. Access to C(sp3)-C(sp2) and C(sp2)-C(sp2) bond formation via sequential intermolecular carbopalladation of multiple carbon-carbon bonds. The Journal of Organic Chemistry. 77: 5418-22. PMID 22647071 DOI: 10.1021/Jo300662X  0.448
2012 Huang L, Wang Q, Liu X, Jiang H. Switch of selectivity in the synthesis of α-methylene-γ-lactones: palladium-catalyzed intermolecular carboesterification of alkenes with alkynes. Angewandte Chemie (International Ed. in English). 51: 5696-700. PMID 22529054 DOI: 10.1002/Anie.201109141  0.442
2012 Jiang H, Pan X, Huang L, Zhao J, Shi D. Synthesis of 4H-cyclopenta[c]furans via cooperative PdCl2-FeCl2 catalyzed cascade cyclization reaction involving a novel acyl rearrangement process. Chemical Communications (Cambridge, England). 48: 4698-700. PMID 22473222 DOI: 10.1039/C2Cc31138K  0.519
2012 Wen Y, Huang L, Jiang H, Chen H. Synthesis of δ-bromo γ,δ-unsaturated carbonyl compounds via palladium-catalyzed bromoalkylation of alkynoates. The Journal of Organic Chemistry. 77: 2029-34. PMID 22283721 DOI: 10.1021/Jo202416H  0.51
2012 Li X, Huang L, Chen H, Wu W, Huang H, Jiang H. Copper-catalyzed oxidative [2 + 2 + 1] cycloaddition: Regioselective synthesis of 1,3-oxazoles from internal alkynes and nitriles Chemical Science. 3: 3463-3467. DOI: 10.1039/C2Sc21041J  0.501
2011 Qi C, Jiang H, Huang L, Yuan G, Ren Y. Carbon dioxide triggered and copper-catalyzed domino reaction: efficient construction of highly substituted 3(2H)-furanones from nitriles and propargylic alcohols. Organic Letters. 13: 5520-3. PMID 21919535 DOI: 10.1021/Ol202241R  0.429
2011 Zhou P, Jiang H, Huang L, Li X. Acetoxypalladation of unactivated alkynes and capture with alkenes to give 1-acetoxy-1,3-dienes taking dioxygen as terminal oxidant. Chemical Communications (Cambridge, England). 47: 1003-5. PMID 21063597 DOI: 10.1039/C0Cc03723K  0.491
2011 Wen Y, Wang A, Jiang H, Zhu S, Huang L. Highly regio- and stereoselective synthesis of 1,3-enynes from unactivated ethylenes via palladium-catalyzed cross-coupling Tetrahedron Letters. 52: 5736-5739. DOI: 10.1016/J.Tetlet.2011.07.092  0.606
2011 Zhou P, Jiang H, Huang L, Li X. ChemInform Abstract: Acetoxypalladation of Unactivated Alkynes and Capture with Alkenes to Give 1-Acetoxy-1,3-dienes Taking Dioxygen as Terminal Oxidant. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201117045  0.321
2011 Zhou P, Huang L, Jiang H, Wang A, Li X. ChemInform Abstract: Highly Chemoselective Palladium-Catalyzed Cross-Trimerization Between Alkyne and Alkenes Leading to 1,3,5-Trienes or 1,2,4,5-Tetrasubstituted Benzenes with Dioxygen. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201111029  0.453
2010 Huang L, Jiang H, Qi C, Liu X. Copper-catalyzed intermolecular oxidative [3 + 2] cycloaddition between alkenes and anhydrides: a new synthetic approach to γ-lactones. Journal of the American Chemical Society. 132: 17652-4. PMID 21114288 DOI: 10.1021/Ja108073K  0.504
2010 Zhou P, Huang L, Jiang H, Wang A, Li X. Highly chemoselective palladium-catalyzed cross-trimerization between alkyne and alkenes leading to 1,3,5-trienes or 1,2,4,5-tetrasubstituted benzenes with dioxygen. The Journal of Organic Chemistry. 75: 8279-82. PMID 21047130 DOI: 10.1021/Jo101554R  0.518
2010 Liu W, Jiang H, Huang L. One-pot silver-catalyzed and PIDa-mediated sequential reactions: synthesis of polysubstituted pyrroles directly from alkynoates and amines. Organic Letters. 12: 312-5. PMID 20000625 DOI: 10.1021/Ol9026478  0.572
2010 Jiang HF, Ye JW, Qi CR, Huang LB. Corrigendum to "Naturally occurring α-amino acid: a simple and inexpensive catalyst for the selective synthesis of 5-aryl-2-oxazolidinones from CO2 and aziridines under solvent-free conditions" [Tetrahedron Lett. 51 (2010) 928] (DOI:10.1016/j.tetlet.2009.12.031) Tetrahedron Letters. 51: 1924. DOI: 10.1016/J.Tetlet.2010.01.043  0.408
2010 Jiang HF, Ye JW, Qi CR, Huang LB. Naturally occurring α-amino acid: a simple and inexpensive catalyst for the selective synthesis of 5-aryl-2-oxazolidinones from CO2 and aziridines under solvent-free conditions Tetrahedron Letters. 51: 928-932. DOI: 10.1016/J.Tetlet.2009.12.031  0.512
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