| Year |
Citation |
Score |
| 2024 |
Zhao Q, Hu J, Gui Z, Chang Z, Zhang C, Chen Y, Huang Y, Zhang P, Wang F. Alanine Production from Chemical Upcycling of Polylactic Acid Waste over Fe Doped Ru/CeO2. Chemsuschem. e202401727. PMID 39329461 DOI: 10.1002/cssc.202401727 |
0.303 |
|
| 2024 |
Wang X, Zhang J, Li L, Zhu Y, Zhang Y, Ni M, Ding Y, Huang Y, Pan Y. Formation mechanism of high biofilm phosphorus storage capacity and its effect on phosphorus uptake-release and carbon source consumption. Bioresource Technology. 131363. PMID 39197659 DOI: 10.1016/j.biortech.2024.131363 |
0.326 |
|
| 2024 |
Zhang JW, Zhang Y, Huang Y. Organocatalytic Atroposelective Synthesis of Axially Chiral Indolyl Ketosulfoxonium Ylides. Angewandte Chemie (International Ed. in English). e202413102. PMID 39105615 DOI: 10.1002/anie.202413102 |
0.398 |
|
| 2024 |
Li E, Liao X, Guo F, Huang Y, Chen J. N-Heterocyclic Carbene-Catalyzed Asymmetric S2 Alkylation via Noncovalent Activation. Organic Letters. PMID 39092835 DOI: 10.1021/acs.orglett.4c02082 |
0.33 |
|
| 2024 |
Ye X, Pan H, Huang Y, Chen J, Wang Z. Photochemical three-component assembly of tri-substituted oxazoles through a carbenic phosphorus-nitrile hybrid ylide formation/trapping cascade. Chemical Science. 15: 6515-6521. PMID 38699275 DOI: 10.1039/d4sc01355g |
0.36 |
|
| 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 |
0.348 |
|
| 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 |
0.358 |
|
| 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 |
0.361 |
|
| 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 |
0.321 |
|
| 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 |
0.685 |
|
| 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 |
0.405 |
|
| 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 |
0.359 |
|
| 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 |
0.355 |
|
| 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 |
0.386 |
|
| 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 |
0.37 |
|
| 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 |
0.366 |
|
| 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 |
0.396 |
|
| 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 |
0.715 |
|
| 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 |
0.335 |
|
| 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 |
0.321 |
|
| 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 |
0.379 |
|
| 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 |
0.685 |
|
| 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 |
0.365 |
|
| 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 |
0.352 |
|
| 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 |
0.324 |
|
| 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 |
0.366 |
|
| 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 |
0.336 |
|
| 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 |
0.356 |
|
| 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 |
0.4 |
|
| 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 |
0.334 |
|
| 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 |
0.344 |
|
| 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 |
0.411 |
|
| 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 |
0.415 |
|
| 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 |
0.306 |
|
| 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 |
0.42 |
|
| 2015 |
Shao Q, Huang Y. Direct fluorination of styrenes. Chemical Communications (Cambridge, England). 51: 6584-6. PMID 25771968 DOI: 10.1039/C5Cc01407G |
0.402 |
|
| 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 |
0.401 |
|
| 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 |
0.371 |
|
| 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 |
0.42 |
|
| 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 |
0.42 |
|
| 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 |
0.349 |
|
| 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 |
0.346 |
|
| 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 |
0.36 |
|
| 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 |
0.593 |
|
| 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 |
0.422 |
|
| 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 |
0.347 |
|
| 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 |
0.579 |
|
| 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 |
0.354 |
|
| 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 |
0.421 |
|
| 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 |
0.342 |
|
| 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 |
0.417 |
|
| 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 |
0.603 |
|
| 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 |
0.408 |
|
| 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 |
0.531 |
|
| 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 |
0.412 |
|
| 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 |
0.559 |
|
| 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 |
0.402 |
|
| 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 |
0.377 |
|
| 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 |
0.373 |
|
| 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 |
0.346 |
|
| 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 |
0.555 |
|
| 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 |
0.35 |
|
| 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 |
0.565 |
|
| 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 |
0.546 |
|
| 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 |
0.522 |
|
| 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 |
0.409 |
|
| 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 |
0.337 |
|
| 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 |
0.501 |
|
| 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 |
0.476 |
|
| 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 |
0.396 |
|
| 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 |
0.658 |
|
| 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 |
0.725 |
|
| 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 |
0.741 |
|
| 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 |
0.641 |
|
| 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 |
0.64 |
|
| 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 |
0.751 |
|
| 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 |
0.637 |
|
| 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 |
0.721 |
|
| 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 |
0.639 |
|
| 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 |
0.615 |
|
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