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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