| Year |
Citation |
Score |
| 2023 |
Wu F, Zhang Y, Zhu R, Huang Y. Discovery and synthesis of atropisomerically chiral acyl-substituted stable vinyl sulfoxonium ylides. Nature Chemistry. PMID 37945832 DOI: 10.1038/s41557-023-01358-z |
0.359 |
|
| 2022 |
Li L, Deng K, Xing Y, Ma C, Ni SF, Wang Z, Huang Y. Synthesis of I/S reagents and their reactivity in photochemical cycloaddition reactions with unsaturated bonds. Nature Communications. 13: 6588. PMID 36329065 DOI: 10.1038/s41467-022-34401-7 |
0.371 |
|
| 2022 |
Liu W, Zhang L, Liao X, Chen J, Huang Y. An NHC-catalyzed [3+2] cyclization of β-disubstituted enals with benzoyl cyanides. Chemical Communications (Cambridge, England). PMID 35924630 DOI: 10.1039/d2cc04025e |
0.374 |
|
| 2022 |
Li E, Chen J, Huang Y. Enantioselective Seleno-Michael Addition Reactions Catalyzed by a Chiral Bifunctional N-Heterocyclic Carbene with Noncovalent Activation. Angewandte Chemie (International Ed. in English). e202202040. PMID 35322507 DOI: 10.1002/anie.202202040 |
0.322 |
|
| 2020 |
Wu F, Wang L, Ji Y, Zou G, Shen H, Nicewicz DA, Chen J, Huang Y. Direct Synthesis of Bicyclic Acetals via Visible Light Catalysis. Iscience. 23: 101395. PMID 32759056 DOI: 10.1016/J.Isci.2020.101395 |
0.691 |
|
| 2020 |
Li L, Chen B, Chen J, Huang Y. Enantioselective intramolecular [2,3]-sigmatropic rearrangement of aldehydes via a sulfonium enamine intermediate. Angewandte Chemie (International Ed. in English). PMID 32757344 DOI: 10.1002/anie.202010234 |
0.302 |
|
| 2019 |
Wang L, Jiang X, Chen J, Huang Y. Enantio- and Diastereoselective Hydrofluorination of Enals via N-Heterocyclic Carbene Catalysis. Angewandte Chemie (International Ed. in English). PMID 30942950 DOI: 10.1002/Anie.201902989 |
0.407 |
|
| 2019 |
Li L, Liu Q, Chen J, Huang Y. Alcohol-Directed ortho-C–H Alkenylation Synlett. 30: 1366-1370. DOI: 10.1055/S-0037-1611538 |
0.361 |
|
| 2018 |
Wang Q, Chen J, Huang Y. Aerobic Oxidation/Annulation Cascades via Synergistic Catalysis of RuCl3 and N-Heterocyclic Carbenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29978509 DOI: 10.1002/Chem.201803254 |
0.356 |
|
| 2018 |
Yuan P, Chen J, Zhao J, Huang Y. Enantioselective hydroamidation of enals by trapping of a transient acyl species. Angewandte Chemie (International Ed. in English). PMID 29693756 DOI: 10.1002/Anie.201803556 |
0.388 |
|
| 2018 |
Peng S, Wang Z, Zhang L, Zhang X, Huang Y. Streamlined asymmetric α-difunctionalization of ynones. Nature Communications. 9: 375. PMID 29371601 DOI: 10.1038/S41467-017-02801-9 |
0.371 |
|
| 2018 |
He Z, Song F, Sun H, Huang Y. A Transition-Metal-Free Suzuki-Type Cross-Coupling Reaction of Benzyl Halides and Boronic Acids via 1,2-Metallate Shift. Journal of the American Chemical Society. PMID 29360376 DOI: 10.1021/Jacs.8B00380 |
0.368 |
|
| 2018 |
Zhang L, Yuan P, Chen J, Huang Y. Enantioselective cooperative proton-transfer catalysis using chiral ammonium phosphates. Chemical Communications (Cambridge, England). PMID 29355859 DOI: 10.1039/C7Cc09549J |
0.397 |
|
| 2018 |
Wu F, Wang L, Chen J, Nicewicz DA, Huang Y. Direct Synthesis of Polysubstituted Aldehydes via Visible-Light-Catalysis. Angewandte Chemie (International Ed. in English). PMID 29316099 DOI: 10.1002/Anie.201712384 |
0.723 |
|
| 2018 |
Wang L, Wang Q, Chen J, Huang Y. Switching Reaction Pathways by Cooperative Catalysis of N-Heterocyclic Carbene and Lewis Acids Acta Chimica Sinica. 76: 850. DOI: 10.6023/A18060244 |
0.336 |
|
| 2018 |
Si Y, Liang L, Tang S, Qi Y, Huang Y, Zheng J. One-pot ligation strategy for atypical ubiquitin chains synthesis by using the trifluoroacetamidomethyl-protected isopeptide-linked Ub (Tfacm-isoUb) unit Tetrahedron Letters. 59: 268-271. DOI: 10.1016/J.Tetlet.2017.12.028 |
0.331 |
|
| 2017 |
Wang Z, He Z, Zhang L, Huang Y. Iridium Catalyzed Aerobic α,β-Dehydrogenation of γ,δ-Unsaturated Amides and Acids: Activation of Both α- and β-C-H bonds through an Allyl-Iridium Intermediate. Journal of the American Chemical Society. PMID 29251918 DOI: 10.1021/Jacs.7B11351 |
0.322 |
|
| 2017 |
Chen J, Pengfei Y, Wang L, Huang Y. Enantioselective β-Protonation of Enals via a Shuttling Strategy. Journal of the American Chemical Society. PMID 28475323 DOI: 10.1021/Jacs.7B02889 |
0.38 |
|
| 2017 |
Wang L, Wu F, Chen J, Nicewicz DA, Huang Y. Visible-Light-Mediated [4+2] Cycloaddition of Styrenes: Synthesis of Tetralin Derivatives. Angewandte Chemie (International Ed. in English). PMID 28474858 DOI: 10.1002/Anie.201702940 |
0.692 |
|
| 2017 |
Wang F, Chen J, Huang Y. Synthesis of Optically Active Oxazolines by an Organocatalytic Isocyanoacetate Aldol Reaction with α-Keto Esters Synlett. 28: 1300-1304. DOI: 10.1055/S-0036-1588718 |
0.366 |
|
| 2017 |
Yang C, Song F, Chen J, Huang Y. Construction of Pyridazine Analogues via Rhodium-mediated C-H Activation Advanced Synthesis & Catalysis. 359: 3496-3502. DOI: 10.1002/Adsc.201700905 |
0.353 |
|
| 2017 |
Li X, Yu H, Huang Y. Amine‐Triggered 6π‐Electrocyclization–Aromatization Cascade of Ynedienamines Advanced Synthesis & Catalysis. 359: 1379-1387. DOI: 10.1002/Adsc.201601146 |
0.325 |
|
| 2016 |
Jiang H, Xu LP, Fang Y, Zhang ZX, Yang Z, Huang Y. A Migratory Ether Formation Route to Medium-Sized Sugar Mimetics. Angewandte Chemie (International Ed. in English). PMID 27735113 DOI: 10.1002/Anie.201608974 |
0.367 |
|
| 2016 |
Sun H, Guimond N, Huang Y. Advances in the development of catalytic tethering directing groups for C-H functionalization reactions. Organic & Biomolecular Chemistry. PMID 27506568 DOI: 10.1039/C6Ob01258B |
0.337 |
|
| 2016 |
Yuan P, Meng S, Chen J, Huang Y. Asymmetric Sulfa-Michael Addition of α,β-Unsaturated Esters/Amides Using a Chiral N-Heterocyclic Carbene as a Noncovalent Organocatalyst Synlett. 27: 1068-1072. DOI: 10.1055/S-0035-1561843 |
0.358 |
|
| 2016 |
He Z, Huang Y. Diverting C–H Annulation Pathways: Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides Acs Catalysis. 6: 7814-7823. DOI: 10.1021/Acscatal.6B02477 |
0.401 |
|
| 2016 |
Sun H, Zhang Y, Chen P, Wu Y, Zhang X, Huang Y. Ligand-Assisted Palladium(II)/(IV) Oxidation forsp3CH Fluorination Advanced Synthesis & Catalysis. 358: 1946-1957. DOI: 10.1002/Adsc.201600015 |
0.336 |
|
| 2015 |
Chen J, Meng S, Wang L, Tang H, Huang Y. Highly enantioselective sulfa-Michael addition reactions using -heterocyclic carbene as a non-covalent organocatalyst. Chemical Science. 6: 4184-4189. PMID 29218184 DOI: 10.1039/c5sc00878f |
0.347 |
|
| 2015 |
Luo C, Wang Z, Huang Y. Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic. Nature Communications. 6: 10041. PMID 26644194 DOI: 10.1038/Ncomms10041 |
0.413 |
|
| 2015 |
Wang L, Chen J, Huang Y. Highly Enantioselective Aza-Michael Reaction between Alkyl Amines and β-Trifluoromethyl β-Aryl Nitroolefins. Angewandte Chemie (International Ed. in English). PMID 26516707 DOI: 10.1002/Anie.201508371 |
0.417 |
|
| 2015 |
Huang Y, Song L, Gong L, Meggers E. Asymmetric Synthesis of Hydrocarbazoles Catalyzed by an Octahedral Chiral-at-Rhodium Lewis Acid. Chemistry, An Asian Journal. PMID 26344422 DOI: 10.1002/Asia.201500764 |
0.308 |
|
| 2015 |
Li X, Peng S, Li L, Huang Y. Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels-Alder reactions. Nature Communications. 6: 6913. PMID 25898310 DOI: 10.1038/Ncomms7913 |
0.422 |
|
| 2015 |
Shao Q, Huang Y. Direct fluorination of styrenes. Chemical Communications (Cambridge, England). 51: 6584-6. PMID 25771968 DOI: 10.1039/C5Cc01407G |
0.403 |
|
| 2015 |
Zhang Y, Wang Q, Yu H, Huang Y. Directed arene/alkyne annulation reactions via aerobic copper catalysis. Organic & Biomolecular Chemistry. 12: 8844-50. PMID 25116130 DOI: 10.1039/C4Ob01312C |
0.402 |
|
| 2015 |
Sun H, Huang Y. Recent Progress in the Development of Multitasking Directing Groups for Carbon–Hydrogen Activation Reactions Synlett. 26: 2751-2762. DOI: 10.1055/S-0035-1560169 |
0.372 |
|
| 2015 |
Chen J, Meng S, Wang L, Tang H, Huang Y. Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst Chemical Science. 6: 4184-4189. DOI: 10.1039/C5Sc00878F |
0.422 |
|
| 2015 |
Chen H, Wang Q, Huang Y. A copper-catalyzed aerobic domino process for the synthesis of isoindolin-1-ylidene derivatives Tetrahedron. 71: 3632-3636. DOI: 10.1016/J.Tet.2014.11.071 |
0.421 |
|
| 2014 |
Zhang Z, Jiang H, Huang Y. Ruthenium-catalyzed redox-neutral C-H activation via N-N cleavage: synthesis of N-substituted indoles. Organic Letters. 16: 5976-9. PMID 25380398 DOI: 10.1021/Ol502998N |
0.351 |
|
| 2014 |
Wang Z, Li L, Huang Y. A general synthesis of ynones from aldehydes via oxidative C-C bond cleavage under aerobic conditions. Journal of the American Chemical Society. 136: 12233-6. PMID 25133731 DOI: 10.1021/Ja506352B |
0.347 |
|
| 2014 |
Chen Y, Wang D, Duan P, Ben R, Dai L, Shao X, Hong M, Zhao J, Huang Y. A multitasking functional group leads to structural diversity using designer C-H activation reaction cascades. Nature Communications. 5: 4610. PMID 25119789 DOI: 10.1038/Ncomms5610 |
0.362 |
|
| 2014 |
Sun H, Wang C, Yang YF, Chen P, Wu YD, Zhang X, Huang Y. Synthesis of indolo[2,1-a]isoquinolines via a triazene-directed C-H annulation cascade. The Journal of Organic Chemistry. 79: 11863-72. PMID 24820526 DOI: 10.1021/Jo500807D |
0.6 |
|
| 2014 |
Chen J, Huang Y. Asymmetric catalysis with N -heterocyclic carbenes as non-covalent chiral templates Nature Communications. 5: 3437-3437. PMID 24599089 DOI: 10.1038/Ncomms4437 |
0.424 |
|
| 2014 |
Cheng T, Yin W, Zhang Y, Zhang Y, Huang Y. Palladium catalyzed acetoxylation of benzylic C-H bonds using a bidentate picolinamide directing group. Organic & Biomolecular Chemistry. 12: 1405-11. PMID 24435470 DOI: 10.1039/C3Ob42196A |
0.348 |
|
| 2014 |
Fang Y, Wang C, Su S, Yu H, Huang Y. Selective synthesis of indazoles and indoles via triazene-alkyne cyclization switched by different metals. Organic & Biomolecular Chemistry. 12: 1061-71. PMID 24357235 DOI: 10.1039/C3Ob42088D |
0.586 |
|
| 2014 |
Yin W, Wang Z, Huang Y. Highly ortho‐Selective Trifluoromethylthiolation Reactions using a Ligand Exchange Strategy Advanced Synthesis & Catalysis. 356: 2998-3006. DOI: 10.1002/Adsc.201400362 |
0.355 |
|
| 2013 |
Wang Z, Li X, Huang Y. Direct α-vinylidenation of aldehydes and subsequent cascade: gold and amine catalysts work synergistically. Angewandte Chemie (International Ed. in English). 52: 14219-23. PMID 24285418 DOI: 10.1002/Anie.201308835 |
0.422 |
|
| 2013 |
Zhang J, Wang L, Liu Q, Yang Z, Huang Y. Synthesis of α,β-unsaturated carbonyl compounds via a visible-light-promoted organocatalytic aerobic oxidation. Chemical Communications (Cambridge, England). 49: 11662-4. PMID 24190501 DOI: 10.1039/C3Cc46778C |
0.343 |
|
| 2013 |
Shao Q, Chen J, Tu M, Piotrowski DW, Huang Y. Enantioselective synthesis of 1,2,4-triazolines catalyzed by a cinchona alkaloid-derived organocatalyst. Chemical Communications (Cambridge, England). 49: 11098-100. PMID 24145477 DOI: 10.1039/C3Cc46757K |
0.418 |
|
| 2013 |
Wang C, Huang Y. Traceless directing strategy: efficient synthesis of N-alkyl indoles via redox-neutral C-H activation. Organic Letters. 15: 5294-7. PMID 24099640 DOI: 10.1021/Ol402523X |
0.611 |
|
| 2013 |
Luo C, Huang Y. A highly diastereo- and enantioselective synthesis of tetrahydroquinolines: quaternary stereogenic center inversion and functionalization. Journal of the American Chemical Society. 135: 8193-8196. PMID 23676113 DOI: 10.1021/Ja4040945 |
0.409 |
|
| 2013 |
Wang C, Sun H, Fang Y, Huang Y. General and efficient synthesis of indoles through triazene-directed C-H annulation. Angewandte Chemie (International Ed. in English). 52: 5795-8. PMID 23606211 DOI: 10.1002/Anie.201301742 |
0.537 |
|
| 2013 |
Cheng T, Meng S, Huang Y. A highly diastereoselective and enantioselective synthesis of polysubstituted pyrrolidines via an organocatalytic dynamic kinetic resolution cascade. Organic Letters. 15: 1958-61. PMID 23565748 DOI: 10.1021/Ol4006129 |
0.414 |
|
| 2013 |
Yin W, Wang C, Huang Y. Highly practical synthesis of nitriles and heterocycles from alcohols under mild conditions by aerobic double dehydrogenative catalysis. Organic Letters. 15: 1850-3. PMID 23560642 DOI: 10.1021/Ol400459Y |
0.566 |
|
| 2013 |
Chen H, Wang Z, Zhang Y, Huang Y. Highly trans-stereoselective synthesis of bicyclic isoxazolidines via copper-catalyzed triple cascade catalysis. The Journal of Organic Chemistry. 78: 3503-9. PMID 23496240 DOI: 10.1021/Jo400215E |
0.404 |
|
| 2013 |
Zhang Q, Yu HZ, Li YT, Liu L, Huang Y, Fu Y. Computational study on mechanism of Rh(III)-catalyzed oxidative Heck coupling of phenol carbamates with alkenes. Dalton Transactions (Cambridge, England : 2003). 42: 4175-84. PMID 23385440 DOI: 10.1039/C3Dt31898B |
0.378 |
|
| 2013 |
Chen H, Wang Z, Zhang Y, Huang Y. Correction to Highly trans-Stereoselective Synthesis of Bicyclic Isoxazolidines via Copper-Catalyzed Triple Cascade Catalysis Journal of Organic Chemistry. 78: 5116-5116. DOI: 10.1021/Jo400866E |
0.375 |
|
| 2013 |
Wang Z, Li X, Huang Y. Inside Back Cover: Direct α‐Vinylidenation of Aldehydes and Subsequent Cascade: Gold and Amine Catalysts Work Synergistically (Angew. Chem. Int. Ed. 52/2013) Angewandte Chemie. 52: 14253-14253. DOI: 10.1002/Anie.201310080 |
0.347 |
|
| 2013 |
Wang C, Sun H, Fang Y, Huang Y. Inside Back Cover: General and Efficient Synthesis of Indoles through Triazene‐Directed C–H Annulation (Angew. Chem. Int. Ed. 22/2013) Angewandte Chemie. 52: 5885-5885. DOI: 10.1002/Anie.201303274 |
0.561 |
|
| 2013 |
Wang Z, Li X, Huang Y. Innenrücktitelbild: Direct α‐Vinylidenation of Aldehydes and Subsequent Cascade: Gold and Amine Catalysts Work Synergistically (Angew. Chem. 52/2013) Angewandte Chemie. 125: 14503-14503. DOI: 10.1002/Ange.201310080 |
0.351 |
|
| 2013 |
Wang C, Sun H, Fang Y, Huang Y. Innenrücktitelbild: General and Efficient Synthesis of Indoles through Triazene‐Directed C–H Annulation (Angew. Chem. 22/2013) Angewandte Chemie. 125: 5999-5999. DOI: 10.1002/Ange.201303274 |
0.572 |
|
| 2012 |
Wang C, Chen H, Wang Z, Chen J, Huang Y. Rhodium(III)-catalyzed C-H activation of arenes using a versatile and removable triazene directing group. Angewandte Chemie (International Ed. in English). 51: 7242-5. PMID 22733572 DOI: 10.1002/Anie.201203230 |
0.551 |
|
| 2012 |
Wang C, Huang Y. Expanding Structural Diversity; Removable and Manipulable Directing Groups for C–H Activation Synlett. 24: 145-149. DOI: 10.1055/S-0032-1317714 |
0.527 |
|
| 2012 |
Wu G, Yin W, Shen HC, Huang Y. One-pot synthesis of useful heterocycles in medicinal chemistry using a cascade strategy Green Chemistry. 14: 580-585. DOI: 10.1039/C2Gc16457D |
0.411 |
|
| 2012 |
Gao W, He Z, Qian Y, Zhao J, Huang Y. General palladium-catalyzed aerobic dehydrogenation to generate double bonds Chemical Science. 3: 883-886. DOI: 10.1039/C1Sc00661D |
0.338 |
|
| 2012 |
Wang C, Chen H, Wang Z, Chen J, Huang Y. Back Cover: Rhodium(III)-Catalyzed CH Activation of Arenes Using a Versatile and Removable Triazene Directing Group (Angew. Chem. Int. Ed. 29/2012) Angewandte Chemie. 51: 7334-7334. DOI: 10.1002/Anie.201204565 |
0.506 |
|
| 2012 |
Wang C, Chen H, Wang Z, Chen J, Huang Y. Rücktitelbild: Rhodium(III)‐Catalyzed CH Activation of Arenes Using a Versatile and Removable Triazene Directing Group (Angew. Chem. 29/2012) Angewandte Chemie. 124: 7448-7448. DOI: 10.1002/Ange.201204565 |
0.48 |
|
| 2010 |
Gao Y, Chang L, Shi H, Liang B, Wongkhan K, Chaiyaveij D, Batsanov A, Marder T, Li C, Yang Z, Huang Y. A Thiourea‐Oxazoline Library with Axial Chirality: Ligand Synthesis and Studies of the Palladium‐Catalyzed Enantioselective Bis(methoxycarbonylation) of Terminal Olefins Advanced Synthesis & Catalysis. 352: 1955-1966. DOI: 10.1002/Adsc.201000070 |
0.398 |
|
| 2007 |
Thadani AN, Huang Y, Rawal VH. Expedient, high-yielding synthesis of silyl-substituted salen ligands. Organic Letters. 9: 3873-6. PMID 17764187 DOI: 10.1021/Ol0713436 |
0.665 |
|
| 2005 |
Huang Y, Walji AM, Larsen CH, MacMillan DW. Enantioselective organo-cascade catalysis. Journal of the American Chemical Society. 127: 15051-3. PMID 16248643 DOI: 10.1021/Ja055545D |
0.723 |
|
| 2003 |
Huang Y, Unni AK, Thadani AN, Rawal VH. Hydrogen bonding: single enantiomers from a chiral-alcohol catalyst. Nature. 424: 146. PMID 12853945 DOI: 10.1038/424146A |
0.74 |
|
| 2002 |
Huang Y, Rawal VH. Hydrogen-bond-promoted hetero-Diels-Alder reactions of unactivated ketones. Journal of the American Chemical Society. 124: 9662-3. PMID 12175197 DOI: 10.1021/Ja0267627 |
0.648 |
|
| 2002 |
Huang Y, Iwama T, Rawal VH. Design and development of highly effective Lewis acid catalysts for enantioselective Diels-Alder reactions. Journal of the American Chemical Society. 124: 5950-1. PMID 12022822 DOI: 10.1021/Ja026088T |
0.646 |
|
| 2002 |
Kozmin SA, Iwama T, Huang Y, Rawal VH. An efficient approach to Aspidosperma alkaloids via [4 + 2] cycloadditions of aminosiloxydienes: stereocontrolled total synthesis of (+/-)-tabersonine. Gram-scale catalytic asymmetric syntheses of (+)-tabersonine and (+)-16-methoxytabersonine. Asymmetric syntheses of (+)-aspidospermidine and (-)-quebrachamine. Journal of the American Chemical Society. 124: 4628-41. PMID 11971711 DOI: 10.1021/Ja017863S |
0.753 |
|
| 2002 |
Huang Y, Iwama T, Rawal VH. Broadly effective enantioselective Diels-Alder reactions of 1-amino-substituted-1,3-butadienes. Organic Letters. 4: 1163-6. PMID 11922808 DOI: 10.1021/Ol0255716 |
0.643 |
|
| 2002 |
Takenaka N, Huang Y, Rawal VH. The first catalytic enantioselective Diels-Alder reactions of 1,2-dihydropyridine: Efficient syntheses of optically active 2-azabicyclo[2.2.2]octanes with chiral BINAM derived Cr(III) salen complexes Tetrahedron. 58: 8299-8305. DOI: 10.1016/S0040-4020(02)00980-8 |
0.725 |
|
| 2000 |
Huang Y, Rawal VH. Hetero Diels-Alder reactions of 1-amino-3-siloxy-1,3-butadienes under strictly thermal conditions. Organic Letters. 2: 3321-3. PMID 11029200 DOI: 10.1021/Ol006404D |
0.645 |
|
| 2000 |
Huang Y, Iwama T, Rawal VH. Highly enantioselective Diels-Alder reactions of 1-amino-3-siloxy-dienes catalyzed by Cr(III)-salen complexes [17] Journal of the American Chemical Society. 122: 7843-7844. DOI: 10.1021/Ja002058J |
0.621 |
|
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