| Year |
Citation |
Score |
| 2023 |
Xia J, Zhu B, Wan Q, Yu Y, Huang S, Zhang J, Huang X. Gold-Catalyzed Cascade Reaction of Diynamides with Allylic Alcohols: A Versatile Platform to Allenamide, 2-Aminofuran and Bridged [2.2.2]Octadiene Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). e202300826. PMID 36973187 DOI: 10.1002/chem.202300826 |
0.365 |
|
| 2022 |
Wan Q, Xin L, Zhang J, Huang X. Efficient access to 1,3,4-trisubstituted pyrroles gold-catalysed cycloisomerization of 1,5-diynes. Organic & Biomolecular Chemistry. PMID 35137761 DOI: 10.1039/d1ob02393d |
0.35 |
|
| 2020 |
Ma L, Ou P, Huang X. Divergent synthesis of 1,3,5-tri and 1,3-disubstituted pyrazoles under transition metal-free conditions. Organic & Biomolecular Chemistry. PMID 32785327 DOI: 10.1039/D0Ob01478H |
0.383 |
|
| 2020 |
Yu Y, Ma L, Xia J, Xin L, Zhu L, Huang X. A Modular Approach to Dibenzo-fused ε-Lactams: Palladium Carbene Bridging C-H Activation and Its Synthetic Application. Angewandte Chemie (International Ed. in English). PMID 32619036 DOI: 10.1002/Anie.202007799 |
0.442 |
|
| 2020 |
Zhang H, Yu Y, Huang X. Facile access to 2,2-diaryl 2H-chromenes through a palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones. Organic & Biomolecular Chemistry. PMID 32596707 DOI: 10.1039/D0Ob00978D |
0.45 |
|
| 2020 |
Liu J, Zhu L, Wan W, Huang X. Gold-Catalyzed Oxidative Cascade Cyclization of 1,3-Diynamides: Polycyclic N-Heterocycle Synthesis via Construction of a Furopyridinyl Core. Organic Letters. PMID 32242410 DOI: 10.1021/Acs.Orglett.0C01086 |
0.45 |
|
| 2020 |
Ren X, Zhu L, Yu Y, Wang ZX, Huang X. Understanding the Chemoselectivity in Palladium-Catalyzed Three-Component Reaction of -Bromobenzaldehyde, -Tosylhydrazone, and Methanol. Organic Letters. PMID 32227902 DOI: 10.1021/Acs.Orglett.0C01040 |
0.376 |
|
| 2020 |
Zhu L, Ren X, Yu Y, Ou P, Wang ZX, Huang X. Palladium-Catalyzed Three-Component Coupling Reaction of -Bromobenzaldehyde, -Tosylhydrazone, and Methanol. Organic Letters. PMID 32078335 DOI: 10.1021/Acs.Orglett.0C00579 |
0.451 |
|
| 2020 |
Yu Y, Chakraborty P, Song J, Zhu L, Li C, Huang X. Easy access to medium-sized lactones through metal carbene migratory insertion enabled 1,4-palladium shift. Nature Communications. 11: 461. PMID 31974346 DOI: 10.1038/S41467-019-14101-5 |
0.426 |
|
| 2020 |
Zhu B, Zhu L, Xia J, Huang S, Huang X. Gold-catalyzed cycloisomerization of enynamides: Regio- and stereoselective approach to tetracyclic spiroindolines Tetrahedron. 131056. DOI: 10.1016/J.Tet.2020.131056 |
0.38 |
|
| 2020 |
Yan C, Yu Y, Peng B, Huang X. Carbene Bridging C–H Activation: Facile Isocoumarin Synthesis Through Palladium‐Catalyzed Reaction of 2‐Pseudohalobenzaldehydes with Aryl Diazoesters European Journal of Organic Chemistry. 2020: 723-727. DOI: 10.1002/Ejoc.201901738 |
0.485 |
|
| 2019 |
Liu J, Chakraborty P, Zhang H, Zhong L, Wang Z, Huang X. Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration Acs Catalysis. 9: 2610-2617. DOI: 10.1021/Acscatal.8B04934 |
0.417 |
|
| 2019 |
Zhang H, Yu Y, Huang S, Huang X. Palladium‐Catalyzed Cascade Reaction of
o
‐Bromobenzaldehydes with
N
‐Sulfonylhydrazones: An Efficient Approach to the Naphthalene Skeleton Advanced Synthesis & Catalysis. 361: 1576-1581. DOI: 10.1002/Adsc.201801637 |
0.33 |
|
| 2018 |
Chen G, Yu Y, Huang X. Palladium-Catalyzed Annulation via Acyl C–H Bond Activation Synlett. 29: 2087-2092. DOI: 10.1055/S-0037-1610025 |
0.44 |
|
| 2018 |
Lin M, Zhu L, Xia J, Yu Y, Chen J, Mao Z, Huang X. Gold‐Catalyzed Oxidative Cyclization of Tryptamine Derived Enynamides: A Stereoselective Approach to Tetracyclic Spiroindolines Advanced Synthesis & Catalysis. 360: 2280-2284. DOI: 10.1002/Adsc.201800001 |
0.309 |
|
| 2017 |
Yu Y, Lu Q, Chen G, Li C, Huang X. Palladium-Catalyzed Intermolecular Acylation of Aryldiazoesters with ortho-Bromobenzaldehydes. Angewandte Chemie (International Ed. in English). PMID 29165904 DOI: 10.1002/Anie.201710317 |
0.458 |
|
| 2017 |
Cheng X, Zhu L, Lin M, Chen J, Huang X. Rapid access to cyclopentadiene derivatives through gold-catalyzed cycloisomerization of ynamides with cyclopropenes by preferential activation of alkenes over alkynes. Chemical Communications (Cambridge, England). PMID 28303268 DOI: 10.1039/C7Cc01368J |
0.479 |
|
| 2017 |
Liao Y, Zhu L, Yu Y, Chen G, Huang X. N-Heterocycle Synthesis via Gold-Catalyzed Intermolecular Nitrene Transfer Reactions of Alkynes Chinese Journal of Organic Chemistry. 37: 2785. DOI: 10.6023/Cjoc201708021 |
0.49 |
|
| 2017 |
Liao Y, Lu Q, Chen G, Yu Y, Li C, Huang X. Rhodium-Catalyzed Azide–Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions Acs Catalysis. 7: 7529-7534. DOI: 10.1021/Acscatal.7B02558 |
0.417 |
|
| 2016 |
Chen G, Song J, Yu Y, Luo X, Li C, Huang X. Aminofluorination: transition-metal-free N-F bond insertion into diazocarbonyl compounds. Chemical Science. 7: 1786-1790. PMID 28959390 DOI: 10.1039/C5Sc04237B |
0.369 |
|
| 2016 |
Yu Y, Chen G, Zhu L, Liao Y, Wu Y, Huang X. Gold-Catalyzed β-Regioselective Formal [3+2] Cycloaddition of Ynamides with Pyrido[1,2-b]indazoles: Reaction Development and Mechanistic Insights. The Journal of Organic Chemistry. PMID 27569125 DOI: 10.1021/Acs.Joc.6B01948 |
0.457 |
|
| 2016 |
Luo X, Chen G, He L, Huang X. Amination of Diazocarbonyl Compounds: N-H Insertion under Metal-Free Conditions. The Journal of Organic Chemistry. PMID 26954790 DOI: 10.1021/Acs.Joc.6B00233 |
0.383 |
|
| 2016 |
Cheng X, Yu Y, Mao Z, Chen J, Huang X. Facile synthesis of substituted 3-aminofurans through a tandem reaction of N-sulfonyl-1,2,3-triazoles with propargyl alcohols. Organic & Biomolecular Chemistry. PMID 26952826 DOI: 10.1039/C6Ob00377J |
0.469 |
|
| 2016 |
Zhang H, Huang X. Ligand‐Free Heck Reactions of Aryl Iodides: Significant Acceleration of the Rate through Visible Light Irradiation at Ambient Temperature Advanced Synthesis & Catalysis. 358: 3736-3742. DOI: 10.1002/Adsc.201600704 |
0.389 |
|
| 2016 |
Yu Y, Zhu L, Liao Y, Mao Z, Huang X. Rhodium(II)-Catalysed Skeletal Rearrangement of Ether Tethered N-Sulfonyl 1,2,3-Triazoles: A Rapid Approach to 2-Aminoindanone and Dihydroisoquinoline Derivatives Advanced Synthesis and Catalysis. 358: 1059-1064. DOI: 10.1002/Adsc.201501178 |
0.355 |
|
| 2015 |
Wu Y, Zhu L, Yu Y, Luo X, Huang X. Polysubstituted 2-Aminopyrrole Synthesis via Gold-Catalyzed Intermolecular Nitrene Transfer from Vinyl Azide to Ynamide: Reaction Scope and Mechanistic Insights. The Journal of Organic Chemistry. PMID 26503292 DOI: 10.1021/Acs.Joc.5B02057 |
0.491 |
|
| 2015 |
Klimczyk S, Misale A, Huang X, Maulide N. Dimeric TADDOL Phosphoramidites in Asymmetric Catalysis: Domino Deracemization and Cyclopropanation of Sulfonium Ylides. Angewandte Chemie (International Ed. in English). PMID 26138505 DOI: 10.1002/Anie.201503851 |
0.587 |
|
| 2015 |
Klimczyk S, Huang X, Kählig H, Veiros LF, Maulide N. Stereoselective gold(I) domino catalysis of allylic isomerization and olefin cyclopropanation: mechanistic studies. The Journal of Organic Chemistry. 80: 5719-29. PMID 26017800 DOI: 10.1021/Acs.Joc.5B00666 |
0.648 |
|
| 2015 |
Zhu L, Yu Y, Mao Z, Huang X. Gold-catalyzed intermolecular nitrene transfer from 2H-azirines to ynamides: a direct approach to polysubstituted pyrroles. Organic Letters. 17: 30-3. PMID 25514612 DOI: 10.1021/Ol503172H |
0.472 |
|
| 2015 |
Klimczyk S, Huang X, Kählig H, Veiros LF, Maulide N. Stereoselective gold(I) domino catalysis of allylic isomerization and olefin cyclopropanation: Mechanistic studies Journal of Organic Chemistry. 80: 5719-5729. DOI: 10.1021/acs.joc.5b00666 |
0.611 |
|
| 2015 |
Klimczyk S, Misale A, Huang X, Maulide N. Dimere TADDOL-Phosphoramidite in der asymmetrischen Katalyse: Domino-Deracemisierung/Cyclopropanierung von Sulfoniumyliden Angewandte Chemie. 127: 10507-10511. DOI: 10.1002/Ange.201503851 |
0.516 |
|
| 2014 |
Sabbatani J, Huang X, Veiros LF, Maulide N. Gold-catalyzed intermolecular synthesis of alkylidenecyclopropanes through catalytic allene activation. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 10636-9. PMID 24976605 DOI: 10.1002/Chem.201402935 |
0.624 |
|
| 2014 |
Peng B, Huang X, Xie LG, Maulide N. A Brønsted acid catalyzed redox arylation. Angewandte Chemie (International Ed. in English). 53: 8718-21. PMID 24590501 DOI: 10.1002/Anie.201310865 |
0.613 |
|
| 2014 |
Sabbatani J, Huang X, Veiros LF, Maulide N. Gold-catalyzed intermolecular synthesis of alkylidenecyclopropanes through catalytic allene activation Chemistry - a European Journal. 20: 10636-10639. DOI: 10.1002/chem.201402935 |
0.589 |
|
| 2014 |
Peng B, Huang X, Xie L, Maulide N. Inside Back Cover: A Brønsted Acid Catalyzed Redox Arylation (Angew. Chem. Int. Ed. 33/2014) Angewandte Chemie International Edition. 53: 8789-8789. DOI: 10.1002/Anie.201406163 |
0.564 |
|
| 2014 |
Peng B, Huang X, Xie LG, Maulide N. A Brønsted acid catalyzed redox arylation Angewandte Chemie - International Edition. 53: 8718-8721. DOI: 10.1002/anie.201310865 |
0.521 |
|
| 2014 |
Peng B, Huang X, Xie L, Maulide N. Innenrücktitelbild: Eine Brønsted-Säure-katalysierte Redox-Arylierung (Angew. Chem. 33/2014) Angewandte Chemie. 126: 8933-8933. DOI: 10.1002/Ange.201406163 |
0.505 |
|
| 2014 |
Peng B, Huang X, Xie L, Maulide N. Eine Brønsted-Säure-katalysierte Redox-Arylierung Angewandte Chemie. 126: 8862-8866. DOI: 10.1002/Ange.201310865 |
0.491 |
|
| 2013 |
Huang X, Patil M, Farès C, Thiel W, Maulide N. Sulfur(IV)-mediated transformations: From ylide transfer to metal-free arylation of carbonyl compounds Journal of the American Chemical Society. 135: 7312-7323. PMID 23641807 DOI: 10.1021/Ja4017683 |
0.602 |
|
| 2013 |
Huang X, Goddard R, Maulide N. Facile carbon-sulfur bond cleavage in diarylsulfonium ylides: a catalytic sulfur-to-silicon group transfer. Chemical Communications (Cambridge, England). 49: 4292-4. PMID 23011230 DOI: 10.1039/C2Cc35762C |
0.571 |
|
| 2013 |
Huang X, Klimczyk S, Veiros LF, Maulide N. Stereoselective intramolecular cyclopropanation through catalytic olefin activation Chemical Science. 4: 1105-1110. DOI: 10.1039/C2Sc21914J |
0.596 |
|
| 2013 |
Huang X, Goddard R, Maulide N. Facile carbon-sulfur bond cleavage in diarylsulfonium ylides: A catalytic sulfur-to-silicon group transfer Chemical Communications. 49: 4292-4294. DOI: 10.1039/c2cc35762c |
0.473 |
|
| 2012 |
Huang X, Peng B, Luparia M, Gomes LF, Veiros LF, Maulide N. Gold-catalyzed synthesis of furans and furanones from sulfur ylides. Angewandte Chemie (International Ed. in English). 51: 8886-90. PMID 22847787 DOI: 10.1002/Anie.201203637 |
0.634 |
|
| 2012 |
Klimczyk S, Huang X, Farès C, Maulide N. Sulfoxide-mediated Umpolung of alkali halide salts. Organic & Biomolecular Chemistry. 10: 4327-9. PMID 22592400 DOI: 10.1039/C2Ob25459J |
0.575 |
|
| 2012 |
Huang X, Klimczyk S, Maulide N. Charge-accelerated sulfonium [3,3]-sigmatropic rearrangements Synthesis. 2012: 175-183. DOI: 10.1055/S-0031-1289632 |
0.675 |
|
| 2012 |
Klimczyk S, Huang X, Farès C, Maulide N. Sulfoxide-mediated Umpolung of alkali halide salts Organic and Biomolecular Chemistry. 10: 4327-4329. DOI: 10.1039/c2ob25459j |
0.475 |
|
| 2012 |
Huang X, Peng B, Luparia M, Gomes LFR, Veiros LF, Maulide N. Gold-katalysierte Synthese von Furanen und Furanonen aus Schwefel-Yliden Angewandte Chemie. 124: 9016-9020. DOI: 10.1002/Ange.201203637 |
0.529 |
|
| 2011 |
Huang X, Maulide N. Sulfoxide-mediated α-arylation of carbonyl compounds. Journal of the American Chemical Society. 133: 8510-3. PMID 21574566 DOI: 10.1021/Ja2031882 |
0.596 |
|
| 2010 |
Huang X, Goddard R, Maulide N. A direct ylide transfer to carbonyl derivatives and heteroaromatic compounds. Angewandte Chemie (International Ed. in English). 49: 8979-83. PMID 20939026 DOI: 10.1002/Anie.201002919 |
0.507 |
|
| 2010 |
Wang T, Huang X, Ye S. Enantioselective formal [2+2] cycloaddition of ketenes with nitroso compounds catalyzed by N-heterocyclic carbenes Organic and Biomolecular Chemistry. 8: 5007-5011. PMID 20820659 DOI: 10.1039/C0Ob00249F |
0.486 |
|
| 2010 |
Sun FG, Huang XL, Ye S. Diastereoselective synthesis of 4-hydroxytetralones via a cascade Stetter-aldol reaction catalyzed by N-heterocyclic carbenes. The Journal of Organic Chemistry. 75: 273-6. PMID 19968291 DOI: 10.1021/Jo902376T |
0.485 |
|
| 2010 |
Huang X, Ye S. Enantioselective benzoin condensation catalyzed by bifunctional N-heterocyclic carbenes Chinese Science Bulletin. 55: 1753-1757. DOI: 10.1007/S11434-010-3122-7 |
0.481 |
|
| 2010 |
Sun F, Huang X, Ye S. ChemInform Abstract: Diastereoselective Synthesis of 4-Hydroxytetralones via a Cascade Stetter-Aldol Reaction Catalyzed by N-Heterocyclic Carbenes. Cheminform. 41. DOI: 10.1002/CHIN.201017098 |
0.385 |
|
| 2010 |
Huang X, Goddard R, Maulide N. Direkter Ylidtransfer auf Carbonylverbindungen und Heteroarene Angewandte Chemie. 122: 9163-9167. DOI: 10.1002/Ange.201002919 |
0.487 |
|
| 2010 |
Lv H, Zhang Y, Huang X, Ye S. Corrigendum: Asymmetric Dimerization of Disubstituted Ketenes Catalyzed by N-Heterocyclic Carbenes Advanced Synthesis & Catalysis. 352: 1218-1218. DOI: 10.1002/Adsc.201090018 |
0.381 |
|
| 2009 |
Huang XL, Chen XY, Ye S. Enantioselective synthesis of aza-beta-lactams via NHC-catalyzed [2 + 2] cycloaddition of ketenes with diazenedicarboxylates. The Journal of Organic Chemistry. 74: 7585-7. PMID 19722509 DOI: 10.1021/Jo901656Q |
0.416 |
|
| 2009 |
Wang X, Lv H, Huang X, Ye S. Asymmetric esterification of ketenes catalyzed by an N-heterocyclic carbene Organic and Biomolecular Chemistry. 7: 346-350. PMID 19109680 DOI: 10.1039/B815139C |
0.415 |
|
| 2009 |
Huang X, He L, Shao P, Ye S. [4+2] Cycloaddition of Ketenes with N‐Benzoyldiazenes Catalyzed by N‐Heterocyclic Carbenes Angewandte Chemie. 48: 192-195. PMID 19040237 DOI: 10.1002/Anie.200804487 |
0.513 |
|
| 2008 |
He L, Zhang Y, Huang X, Ye S. Chiral Bifunctional N-HeterocyclicCarbenes: Synthesis and Application in the Aza-Morita-Baylis-HillmanReaction Synthesis. 2008: 2825-2829. DOI: 10.1055/S-2008-1067216 |
0.426 |
|
| 2008 |
Lv H, Zhang Y, Huang X, Ye S. Asymmetric Dimerization of Disubstituted Ketenes Catalyzed by N‐Heterocyclic Carbenes Advanced Synthesis & Catalysis. 350: 2715-2718. DOI: 10.1002/Adsc.200800532 |
0.4 |
|
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