| Year |
Citation |
Score |
| 2023 |
Wang ZY, Freas DJ, Fu GC. Phosphine Catalysis of the Fluorination of Unactivated Tertiary Alkyl Chlorides under Mild and Convenient Conditions. Journal of the American Chemical Society. 145: 25093-25097. PMID 37939003 DOI: 10.1021/jacs.3c11042 |
0.837 |
|
| 2023 |
Tong X, Yang ZP, Del Angel Aguilar CE, Fu GC. Iron-Catalyzed Reductive Cross-Coupling of Alkyl Electrophiles with Olefins. Angewandte Chemie (International Ed. in English). e202306663. PMID 37391384 DOI: 10.1002/anie.202306663 |
0.785 |
|
| 2023 |
Chen C, Fu GC. Copper-Catalyzed Enantioconvergent Alkylation of Oxygen Nucleophiles. Nature. PMID 36996870 DOI: 10.1038/s41586-023-06001-y |
0.802 |
|
| 2023 |
Zuccarello G, Batiste SM, Cho H, Fu GC. Enantioselective Synthesis of α-Aminoboronic Acid Derivatives via Copper-Catalyzed N-Alkylation. Journal of the American Chemical Society. PMID 36745524 DOI: 10.1021/jacs.3c00038 |
0.411 |
|
| 2022 |
Tong X, Schneck F, Fu GC. Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles. Journal of the American Chemical Society. 144: 14856-14863. PMID 35925763 DOI: 10.1021/jacs.2c06154 |
0.478 |
|
| 2022 |
Cho H, Suematsu H, Oyala PH, Peters JC, Fu GC. Photoinduced, Copper-Catalyzed Enantioconvergent Alkylations of Anilines by Racemic Tertiary Electrophiles: Synthesis and Mechanism. Journal of the American Chemical Society. 144: 4550-4558. PMID 35253433 DOI: 10.1021/jacs.1c12749 |
0.496 |
|
| 2022 |
Lee H, Ahn JM, Oyala PH, Citek C, Yin H, Fu GC, Peters JC. Investigation of the C-N Bond-Forming Step in a Photoinduced, Copper-Catalyzed Enantioconvergent N-Alkylation: Characterization and Application of a Stabilized Organic Radical as a Mechanistic Probe. Journal of the American Chemical Society. PMID 35167268 DOI: 10.1021/jacs.1c13151 |
0.653 |
|
| 2021 |
Chen C, Peters JC, Fu GC. Photoinduced copper-catalysed asymmetric amidation via ligand cooperativity. Nature. PMID 34182570 DOI: 10.1038/s41586-021-03730-w |
0.815 |
|
| 2021 |
Yang ZP, Freas DJ, Fu GC. Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling. Journal of the American Chemical Society. PMID 34080836 DOI: 10.1021/jacs.1c03903 |
0.84 |
|
| 2021 |
Yang ZP, Freas DJ, Fu GC. The Asymmetric Synthesis of Amines via Nickel-Catalyzed Enantioconvergent Substitution Reactions. Journal of the American Chemical Society. PMID 33567209 DOI: 10.1021/jacs.0c13034 |
0.853 |
|
| 2021 |
Wang Z, Yang ZP, Fu GC. Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides. Nature Chemistry. PMID 33432109 DOI: 10.1038/s41557-020-00609-7 |
0.873 |
|
| 2020 |
Yang ZP, Fu GC. Convergent Catalytic Asymmetric Synthesis of Esters of Chiral Dialkyl Carbinols. Journal of the American Chemical Society. PMID 32176494 DOI: 10.1021/Jacs.0C01324 |
0.839 |
|
| 2020 |
Bartoszewicz A, Matier CD, Fu GC. Correction to "Enantioconvergent Alkylations of Amines by Alkyl Electrophiles: Copper-Catalyzed Nucleophilic Substitutions of Racemic α-Halolactams by Indoles". Journal of the American Chemical Society. PMID 32022551 DOI: 10.1021/jacs.0c00943 |
0.646 |
|
| 2020 |
Huo H, Gorsline BJ, Fu GC. Catalyst-controlled doubly enantioconvergent coupling of racemic alkyl nucleophiles and electrophiles. Science (New York, N.Y.). 367: 559-564. PMID 32001652 DOI: 10.1126/science.aaz3855 |
0.828 |
|
| 2019 |
Masuda Y, Fu GC. Synthesis of chiral diamine ligands for nickel-catalyzed asymmetric cross-couplings of alkylchloroboronate esters with alkylzincs: (1,2)-,'-dimethyl-1,2-bis(2-methylphenyl)-1,2-diaminoethane. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 96: 245-257. PMID 32158057 DOI: 10.15227/Orgsyn.096.0245 |
0.54 |
|
| 2019 |
Yin H, Fu GC. Mechanistic Investigation of Enantioconvergent Kumada Reactions of Racemic α-Bromoketones Catalyzed by a Nickel/Bis(oxazoline) Complex. Journal of the American Chemical Society. PMID 31502449 DOI: 10.1021/jacs.9b08185 |
0.704 |
|
| 2019 |
Bartoszewicz A, Matier CD, Fu GC. Enantioconvergent Alkylations of Amines by Alkyl Electrophiles: Copper-Catalyzed Nucleophilic Substitutions of Racemic α-Halolactams by Indoles. Journal of the American Chemical Society. PMID 31496239 DOI: 10.1021/jacs.9b07875 |
0.695 |
|
| 2019 |
Fu GC. Enantioconvergent Cross-Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes. Angewandte Chemie (International Ed. in English). PMID 30650228 DOI: 10.1002/anie.201814208 |
0.522 |
|
| 2018 |
He J, Chen C, Fu GC, Peters JC. Visible-Light-Induced, Copper-Catalyzed Three-Component Coupling of Alkyl Halides, Olefins, and Trifluoromethylthiolate to Generate Trifluoromethyl Thioethers. Acs Catalysis. 8: 11741-11748. PMID 31396434 DOI: 10.1021/Acscatal.8B04094 |
0.786 |
|
| 2018 |
Wang Z, Yin H, Fu GC. Catalytic enantioconvergent coupling of secondary and tertiary electrophiles with olefins. Nature. PMID 30337711 DOI: 10.1038/s41586-018-0669-y |
0.853 |
|
| 2018 |
Fu GC, Wang Z, Bachman S, Dudnik A. Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles. Angewandte Chemie (International Ed. in English). PMID 30079625 DOI: 10.1002/anie.201806015 |
0.867 |
|
| 2017 |
Ahn JM, Peters JC, Fu GC. Design of a Photoredox Catalyst that Enables the Direct Synthesis of Carbamate-Protected Primary Amines via Photoinduced, Copper-Catalyzed N-Alkylation Reactions of Unactivated Secondary Halides. Journal of the American Chemical Society. 139: 18101-18106. PMID 29200268 DOI: 10.1021/Jacs.7B10907 |
0.597 |
|
| 2017 |
Matier CD, Schwaben J, Peters JC, Fu GC. Copper-Catalyzed Alkylation of Aliphatic Amines Induced by Visible Light. Journal of the American Chemical Society. 139: 17707-17710. PMID 29182328 DOI: 10.1021/Jacs.7B09582 |
0.48 |
|
| 2017 |
Zhao W, Wurz RP, Peters JC, Fu GC. Photoinduced, Copper-Catalyzed Decarboxylative C-N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement. Journal of the American Chemical Society. PMID 28841018 DOI: 10.1021/Jacs.7B07546 |
0.453 |
|
| 2017 |
Ahn JM, Ratani TS, Hannoun K, Fu GC, Peters JC. Photoinduced, Copper-Catalyzed Alkylation of Amines: A Mechanistic Study of the Cross-Coupling of Carbazole with Alkyl Bromides. Journal of the American Chemical Society. PMID 28817770 DOI: 10.1021/Jacs.7B07052 |
0.404 |
|
| 2017 |
Fu GC. Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes. Acs Central Science. 3: 692-700. PMID 28776010 DOI: 10.1021/acscentsci.7b00212 |
0.359 |
|
| 2017 |
Mu X, Shibata Y, Makida Y, Fu GC. Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 28421708 DOI: 10.1002/Anie.201702402 |
0.803 |
|
| 2017 |
Choi J, Fu GC. Transition metal-catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry. Science (New York, N.Y.). 356. PMID 28408546 DOI: 10.1126/science.aaf7230 |
0.774 |
|
| 2017 |
Kalek M, Fu GC. Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species. Journal of the American Chemical Society. PMID 28276679 DOI: 10.1021/Jacs.7B01826 |
0.705 |
|
| 2016 |
Johnson MW, Hannoun KI, Tan Y, Fu GC, Peters JC. A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide. Chemical Science. 7: 4091-4100. PMID 28044096 DOI: 10.1039/C5Sc04709A |
0.315 |
|
| 2016 |
Schmidt J, Choi J, Liu AT, Slusarczyk M, Fu GC. A general, modular method for the catalytic asymmetric synthesis of alkylboronate esters. Science (New York, N.Y.). 354: 1265-1269. PMID 27940868 DOI: 10.1126/Science.Aai8611 |
0.846 |
|
| 2016 |
Ziegler DT, Fu GC. Catalytic Enantioselective Carbon-Oxygen Bond Formation: Phosphine-Catalyzed Synthesis of Benzylic Ethers via the Oxidation of Benzylic C-H Bonds. Journal of the American Chemical Society. PMID 27618638 DOI: 10.1021/jacs.6b08486 |
0.456 |
|
| 2016 |
Chu CK, Liang Y, Fu GC. Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles. Journal of the American Chemical Society. PMID 27187869 DOI: 10.1021/jacs.6b03465 |
0.597 |
|
| 2016 |
Kainz QM, Matier CD, Bartoszewicz A, Zultanski SL, Peters JC, Fu GC. Asymmetric copper-catalyzed C-N cross-couplings induced by visible light. Science (New York, N.Y.). 351: 681-4. PMID 26912852 DOI: 10.1126/Science.Aad8313 |
0.648 |
|
| 2016 |
Zuo Z, Cong H, Li W, Choi J, Fu GC, MacMillan DW. Enantioselective Decarboxylative Arylation of α-Amino Acids via the Merger of Photoredox and Nickel Catalysis. Journal of the American Chemical Society. PMID 26849354 DOI: 10.1021/Jacs.5B13211 |
0.826 |
|
| 2016 |
Lautens M, Yoon H, Kainz QM, Matier CD, Bartoszewicz A, Zultanski SL, Peters JC, Fu GC. Asymmetric Photoinduced Copper-Catalyzed C–N Coupling of Alkyl Chlorides Synfacts. 12: 827-827. DOI: 10.1055/S-0035-1562664 |
0.578 |
|
| 2015 |
Ratani TS, Bachman S, Fu GC, Peters JC. Photoinduced, Copper-Catalyzed Carbon-Carbon Bond Formation with Alkyl Electrophiles: Cyanation of Unactivated Secondary Alkyl Chlorides at Room Temperature. Journal of the American Chemical Society. 137: 13902-7. PMID 26491957 DOI: 10.1021/Jacs.5B08452 |
0.43 |
|
| 2015 |
Liang Y, Fu GC. Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF3 and an Alkyl Group. Journal of the American Chemical Society. PMID 26203662 DOI: 10.1021/jacs.5b04725 |
0.469 |
|
| 2015 |
Kalek M, Fu GC. Phosphine-Catalyzed Doubly Stereoconvergent γ-Additions of Racemic Heterocycles to Racemic Allenoates: The Catalytic Enantioselective Synthesis of Protected α,α-Disubstituted α-Amino Acid Derivatives. Journal of the American Chemical Society. 137: 9438-42. PMID 26192217 DOI: 10.1021/Jacs.5B05528 |
0.722 |
|
| 2015 |
Liang Y, Fu GC. Nickel-Catalyzed Alkyl-Alkyl Cross-Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent. Angewandte Chemie (International Ed. in English). PMID 26073669 DOI: 10.1002/anie.201503297 |
0.488 |
|
| 2015 |
Lee SY, Fujiwara Y, Nishiguchi A, Kalek M, Fu GC. Phosphine-catalyzed enantioselective intramolecular [3+2] annulations to generate fused ring systems. Journal of the American Chemical Society. 137: 4587-91. PMID 25815702 DOI: 10.1021/Jacs.5B01985 |
0.85 |
|
| 2015 |
Kramer S, Fu GC. Use of a new spirophosphine to achieve catalytic enantioselective [4 + 1] annulations of amines with allenes to generate dihydropyrroles. Journal of the American Chemical Society. 137: 3803-6. PMID 25780940 DOI: 10.1021/Jacs.5B01944 |
0.678 |
|
| 2014 |
Schley ND, Fu GC. Nickel-catalyzed Negishi arylations of propargylic bromides: a mechanistic investigation. Journal of the American Chemical Society. 136: 16588-93. PMID 25402209 DOI: 10.1021/Ja508718M |
0.701 |
|
| 2014 |
Ziegler DT, Riesgo L, Ikeda T, Fujiwara Y, Fu GC. Biphenyl-derived phosphepines as chiral nucleophilic catalysts: enantioselective [4+1] annulations to form functionalized cyclopentenes. Angewandte Chemie (International Ed. in English). 53: 13183-7. PMID 25287684 DOI: 10.1002/Anie.201405854 |
0.711 |
|
| 2014 |
Choi J, Martín-Gago P, Fu GC. Stereoconvergent arylations and alkenylations of unactivated alkyl electrophiles: catalytic enantioselective synthesis of secondary sulfonamides and sulfones. Journal of the American Chemical Society. 136: 12161-5. PMID 25127186 DOI: 10.1021/Ja506885S |
0.865 |
|
| 2014 |
Lee SY, Neufeind S, Fu GC. Enantioselective nucleophile-catalyzed synthesis of tertiary alkyl fluorides via the α-fluorination of ketenes: synthetic and mechanistic studies. Journal of the American Chemical Society. 136: 8899-902. PMID 24922581 DOI: 10.1021/Ja5044209 |
0.67 |
|
| 2014 |
Liang Y, Fu GC. Catalytic asymmetric synthesis of tertiary alkyl fluorides: Negishi cross-couplings of racemic α,α-dihaloketones. Journal of the American Chemical Society. 136: 5520-4. PMID 24678878 DOI: 10.1021/Ja501815P |
0.556 |
|
| 2014 |
Cong H, Fu GC. Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles. Journal of the American Chemical Society. 136: 3788-91. PMID 24575754 DOI: 10.1021/Ja500706V |
0.554 |
|
| 2014 |
Do HQ, Bachman S, Bissember AC, Peters JC, Fu GC. Photoinduced, copper-catalyzed alkylation of amides with unactivated secondary alkyl halides at room temperature. Journal of the American Chemical Society. 136: 2162-7. PMID 24446666 DOI: 10.1021/Ja4126609 |
0.839 |
|
| 2014 |
Tan Y, Muñoz-Molina JM, Fu GC, Peters JC. Oxygen nucleophiles as reaction partners in photoinduced, copper-catalyzed cross-couplings: O-arylations of phenols at room temperature Chemical Science. 5: 2831-2835. DOI: 10.1039/C4Sc00368C |
0.514 |
|
| 2013 |
Do HQ, Chandrashekar ER, Fu GC. Nickel/bis(oxazoline)-catalyzed asymmetric Negishi arylations of racemic secondary benzylic electrophiles to generate enantioenriched 1,1-diarylalkanes. Journal of the American Chemical Society. 135: 16288-91. PMID 24164502 DOI: 10.1021/Ja408561B |
0.781 |
|
| 2013 |
Ziegler DT, Choi J, Muñoz-Molina JM, Bissember AC, Peters JC, Fu GC. A versatile approach to Ullmann C-N couplings at room temperature: new families of nucleophiles and electrophiles for photoinduced, copper-catalyzed processes. Journal of the American Chemical Society. 135: 13107-12. PMID 23968565 DOI: 10.1021/Ja4060806 |
0.844 |
|
| 2013 |
Cordier CJ, Lundgren RJ, Fu GC. Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine. Journal of the American Chemical Society. 135: 10946-9. PMID 23869442 DOI: 10.1021/Ja4054114 |
0.82 |
|
| 2013 |
Uyeda C, Tan Y, Fu GC, Peters JC. A new family of nucleophiles for photoinduced, copper-catalyzed cross-couplings via single-electron transfer: reactions of thiols with aryl halides under mild conditions (O °C). Journal of the American Chemical Society. 135: 9548-52. PMID 23697882 DOI: 10.1021/Ja404050F |
0.431 |
|
| 2013 |
Bissember AC, Lundgren RJ, Creutz SE, Peters JC, Fu GC. Transition-metal-catalyzed alkylations of amines with alkyl halides: photoinduced, copper-catalyzed couplings of carbazoles. Angewandte Chemie (International Ed. in English). 52: 5129-33. PMID 23564657 DOI: 10.1002/Anie.201301202 |
0.825 |
|
| 2013 |
Lundgren RJ, Wilsily A, Marion N, Ma C, Chung YK, Fu GC. Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoates. Angewandte Chemie (International Ed. in English). 52: 2525-8. PMID 23339132 DOI: 10.1002/Anie.201208957 |
0.852 |
|
| 2013 |
Zultanski SL, Fu GC. Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations. Journal of the American Chemical Society. 135: 624-7. PMID 23281960 DOI: 10.1021/Ja311669P |
0.578 |
|
| 2012 |
Creutz SE, Lotito KJ, Fu GC, Peters JC. Photoinduced Ullmann C-N coupling: demonstrating the viability of a radical pathway. Science (New York, N.Y.). 338: 647-51. PMID 23118186 DOI: 10.1126/Science.1226458 |
0.452 |
|
| 2012 |
Binder JT, Cordier CJ, Fu GC. Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents. Journal of the American Chemical Society. 134: 17003-6. PMID 23039358 DOI: 10.1021/Ja308460Z |
0.73 |
|
| 2012 |
Lee SY, Murphy JM, Ukai A, Fu GC. Nonenzymatic dynamic kinetic resolution of secondary alcohols via enantioselective acylation: synthetic and mechanistic studies. Journal of the American Chemical Society. 134: 15149-53. PMID 22934603 DOI: 10.1021/Ja307425G |
0.591 |
|
| 2012 |
Bissember AC, Levina A, Fu GC. A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies. Journal of the American Chemical Society. 134: 14232-7. PMID 22905894 DOI: 10.1021/Ja306323X |
0.775 |
|
| 2012 |
Dudnik AS, Fu GC. Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds. Journal of the American Chemical Society. 134: 10693-7. PMID 22668072 DOI: 10.1021/Ja304068T |
0.8 |
|
| 2012 |
Choi J, Fu GC. Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent Negishi arylations and alkenylations of racemic α-bromonitriles. Journal of the American Chemical Society. 134: 9102-5. PMID 22612264 DOI: 10.1021/Ja303442Q |
0.839 |
|
| 2012 |
Wilsily A, Tramutola F, Owston NA, Fu GC. New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles. Journal of the American Chemical Society. 134: 5794-7. PMID 22443409 DOI: 10.1021/Ja301612Y |
0.841 |
|
| 2012 |
Zuhl AM, Mohr JT, Bachovchin DA, Niessen S, Hsu KL, Berlin JM, Dochnahl M, López-Alberca MP, Fu GC, Cravatt BF. Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition. Journal of the American Chemical Society. 134: 5068-71. PMID 22400490 DOI: 10.1021/Ja300799T |
0.767 |
|
| 2012 |
Oelke AJ, Sun J, Fu GC. Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group. Journal of the American Chemical Society. 134: 2966-9. PMID 22296603 DOI: 10.1021/Ja300031W |
0.775 |
|
| 2011 |
Fujiwara Y, Sun J, Fu GC. Enantioselective Carbon-Sulfur Bond Formation: γ Additions of Aryl Thiols to Allenoates Catalyzed by a Chiral Phosphepine. Chemical Science (Royal Society of Chemistry : 2010). 2: 2196-2198. PMID 22216403 DOI: 10.1039/C1Sc00414J |
0.766 |
|
| 2011 |
Zultanski SL, Fu GC. Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings. Journal of the American Chemical Society. 133: 15362-4. PMID 21913638 DOI: 10.1021/Ja2079515 |
0.56 |
|
| 2011 |
Fujiwara Y, Fu GC. Application of a new chiral phosphepine to the catalytic asymmetric synthesis of highly functionalized cyclopentenes that bear an array of heteroatom-substituted quaternary stereocenters. Journal of the American Chemical Society. 133: 12293-7. PMID 21766794 DOI: 10.1021/Ja2049012 |
0.577 |
|
| 2011 |
Lu Z, Wilsily A, Fu GC. Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides. Journal of the American Chemical Society. 133: 8154-7. PMID 21553917 DOI: 10.1021/Ja203560Q |
0.869 |
|
| 2011 |
Bachovchin DA, Mohr JT, Speers AE, Wang C, Berlin JM, Spicer TP, Fernandez-Vega V, Chase P, Hodder PS, Schürer SC, Nomura DK, Rosen H, Fu GC, Cravatt BF. Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors. Proceedings of the National Academy of Sciences of the United States of America. 108: 6811-6. PMID 21398589 DOI: 10.1073/Pnas.1015248108 |
0.763 |
|
| 2011 |
Fujiwara Y, Sun J, Fu GC. Synthesis of Aryl Alkyl Sulfides by γ-Addition ofAryl Thiols to Allenoates Synfacts. 2011: 1243-1243. DOI: 10.1055/S-0031-1289266 |
0.542 |
|
| 2011 |
Lu Z, Wilsily A, Fu GC. Amine-Directed Alkyl-Alkyl Suzuki Reactions Synfacts. 2011: 885-885. DOI: 10.1055/S-0030-1260728 |
0.684 |
|
| 2011 |
Lou S, Fu GC. Nickel‐Catalyzed Enantioselective Negishi Cross‐Couplings of Racemic Secondary α‐Bromo Amides with Alkylzinc Reagents: (S)‐N‐Benzyl‐7‐Cyano‐2‐Ethyl‐N‐Phenylheptanamide Organic Syntheses. 87: 330-338. DOI: 10.1002/0471264229.Os087.35 |
0.436 |
|
| 2011 |
Lou S, Fu GC. Palladium‐Catalyzed Alkyl‐Alkyl Suzuki Cross‐Couplings of Primary Alkyl Bromides at Room Temperature: (13‐Chlorotridecyloxy)Triethylsilane Organic Syntheses. 299-309. DOI: 10.1002/0471264229.Os087.32 |
0.52 |
|
| 2010 |
Lou S, Fu GC. SYNTHESIS OF CHIRAL PYRIDINE BIS(OXAZOLINE) LIGANDS FOR NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: 2,6-BIS[(4S)-4,5-DIHYDRO-4-(2-PHENYLETHYL)-2-OXAZOLYL]-PYRIDINE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 87: 310-316. PMID 21614149 DOI: 10.1002/0471264229.Os087.33 |
0.503 |
|
| 2010 |
Lou S, Fu GC. NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: (S,E)-ETHYL 6-(1,3-DIOXOLAN-2-YL)-4-METHYLHEX-2-ENOATE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 87: 317. PMID 21614144 DOI: 10.1002/0471264229.Os087.34 |
0.456 |
|
| 2010 |
Lou S, Fu GC. NICKEL-CATALYZED ENANTIOSELECTIVE NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY α-BROMO AMIDES WITH ALKYLZINC REAGENTS: (S)-N-BENZYL-7-CYANO-2-ETHYL-N-PHENYLHEPTANAMIDE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 87: 330. PMID 21533010 |
0.323 |
|
| 2010 |
Lou S, Fu GC, Higo T, Fukuyama T. PALLADIUM-CATALYZED ALKYL-ALKYL SUZUKI CROSS-COUPLINGS OF PRIMARY ALKYL BROMIDES AT ROOM-TEMPERATURE: (13-CHLOROTRIDECYLOXY)TRIETHYLSILANE [Silane, [(13-chlorotridecyl)oxy]triethyl-]. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 87: 299. PMID 21494316 DOI: 10.15227/Orgsyn.087.0299 |
0.504 |
|
| 2010 |
Lou S, Fu GC. Pd/P(t-Bu)(3)-Catalyzed Suzuki Cross-Couplings in the Presence of Water. Advanced Synthesis & Catalysis. 352: 2081-2084. PMID 21197389 DOI: 10.1002/Adsc.201000267 |
0.379 |
|
| 2010 |
Lu Z, Fu GC. Alkyl-alkyl Suzuki cross-coupling of unactivated secondary alkyl chlorides. Angewandte Chemie (International Ed. in English). 49: 6676-8. PMID 20715038 DOI: 10.1002/Anie.201003272 |
0.732 |
|
| 2010 |
Owston NA, Fu GC. Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins. Journal of the American Chemical Society. 132: 11908-9. PMID 20701271 DOI: 10.1021/Ja105924F |
0.602 |
|
| 2010 |
Lundin PM, Fu GC. Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides. Journal of the American Chemical Society. 132: 11027-9. PMID 20698665 DOI: 10.1021/Ja105148G |
0.42 |
|
| 2010 |
Sinisi R, Sun J, Fu GC. Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides. Proceedings of the National Academy of Sciences of the United States of America. 107: 20652-4. PMID 20624987 DOI: 10.1073/Pnas.1003597107 |
0.758 |
|
| 2010 |
Lou S, Fu GC. Enantioselective alkenylation via nickel-catalyzed cross-coupling with organozirconium reagents. Journal of the American Chemical Society. 132: 5010-1. PMID 20302338 DOI: 10.1021/Ja1017046 |
0.553 |
|
| 2010 |
Sun J, Fu GC. Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters. Journal of the American Chemical Society. 132: 4568-9. PMID 20222657 DOI: 10.1021/Ja101251D |
0.746 |
|
| 2010 |
Lou S, Fu GC. Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones. Journal of the American Chemical Society. 132: 1264-6. PMID 20050651 DOI: 10.1021/Ja909689T |
0.537 |
|
| 2010 |
Wilson JE, Sun J, Fu GC. Stereoselective phosphine-catalyzed synthesis of highly functionalized diquinanes. Angewandte Chemie (International Ed. in English). 49: 161-3. PMID 19943302 DOI: 10.1002/Anie.200905125 |
0.797 |
|
| 2010 |
Fu G, Lu Z. Csp³-Csp³Suzuki Cross-Coupling Using Unactivated Secondary Alkyl Chlorides Synfacts. 2010: 1404-1404. DOI: 10.1055/S-0030-1258849 |
0.317 |
|
| 2010 |
Fu G, Lundin P. Asymmetric Suzuki Cross-Coupling of Secondary Alkyl Electrophiles Synfacts. 2010: 1277-1277. DOI: 10.1055/s-0030-1258798 |
0.359 |
|
| 2010 |
Lou S, Fu GC. ChemInform Abstract: Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201103047 |
0.337 |
|
| 2010 |
Sun J, Fu GC. ChemInform Abstract: Phosphine-Catalyzed Formation of Carbon-Sulfur Bonds: Catalytic Asymmetric Synthesis of γ-Thioesters. Cheminform. 41: no-no. DOI: 10.1002/chin.201030051 |
0.722 |
|
| 2010 |
Kirchhoff JH, Dai C, Fu GC. ChemInform Abstract: A Method for Palladium-Catalyzed Cross-Couplings of Simple Alkyl Chlorides: Suzuki Reactions Catalyzed by [Pd2(dba)3]/PCy3. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200238054 |
0.396 |
|
| 2010 |
Tanaka K, Fu GC. ChemInform Abstract: A Novel Rhodium-Catalyzed Reduction-Oxidation Process: Reaction of 4-Alkynals with Phenol to Provide cis-4-Alkenoates. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200236074 |
0.316 |
|
| 2010 |
Netherton MR, Dai C, Neuschuetz K, Fu GC. ChemInform Abstract: Room-Temperature Alkyl-Alkyl Suzuki Cross-Coupling of Alkyl Bromides that Possess β Hydrogens. Cheminform. 33: no-no. DOI: 10.1002/chin.200205050 |
0.76 |
|
| 2010 |
Littke AF, Fu GC. ChemInform Abstract: A Versatile Catalyst for Heck Reactions of Aryl Chlorides and Aryl Bromides under Mild Conditions. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200144068 |
0.444 |
|
| 2010 |
Fu GC. ChemInform Abstract: Asymmetric Catalysis with “Planar-Chiral” Heterocycles Cheminform. 32: no-no. DOI: 10.1002/CHIN.200142293 |
0.419 |
|
| 2010 |
Dai C, Fu GC. ChemInform Abstract: The First General Method for Palladium-Catalyzed Negishi Cross-Coupling of Aryl and Vinyl Chlorides: Use of Commercially Available Pd(P(t-Bu)3)2 as a Catalyst. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200132058 |
0.351 |
|
| 2010 |
Lo MM, Fu GC. ChemInform Abstract: Applications of Planar-Chiral Heterocycles in Enantioselective Catalysis: Cu(I)/Bisazaferrocene-Catalyzed Asymmetric Ring Expansion of Oxetanes to Tetrahydrofurans. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200129118 |
0.344 |
|
| 2010 |
Fu GC. ChemInform Abstract: Enantioselective Nucleophilic Catalysis with “Planar-Chiral” Heterocycles Cheminform. 31: no-no. DOI: 10.1002/CHIN.200036271 |
0.47 |
|
| 2010 |
Littke AF, Dai C, Fu GC. ChemInform Abstract: Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200031067 |
0.415 |
|
| 2010 |
Ie Y, Fu GC. ChemInform Abstract: A New Benchmark for the Non-enzymatic Enantioselective Acylation of Amines: Use of a Planar-Chiral Derivative of 4-Pyrrolidinopyridine as the Acylating Agent. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200026082 |
0.337 |
|
| 2010 |
Rios R, Liang J, Lo MM, Fu GC. ChemInform Abstract: Synthesis, Resolution, and Crystallographic Characterization of a New C2-Symmetric Planar-Chiral Bipyridine Ligand: Application to the Catalytic Enantioselective Cyclopropanation of Olefins. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200026077 |
0.39 |
|
| 2010 |
Littke AF, Fu GC. ChemInform Abstract: The First General Method for Stille Cross-Couplings of Aryl Chlorides. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199951061 |
0.322 |
|
| 2010 |
Hays DS, Fu GC. ChemInform Abstract: The Development of a New Catalytic Process: Bu3SnH-Catalyzed Reductive Cyclization of Enals and Enones. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199946048 |
0.382 |
|
| 2010 |
Tao B, Ruble JC, Hoic DA, Fu GC. ChemInform Abstract: Non-Enzymatic Kinetic Resolution of Propargylic Alcohols by a Planar-Chiral DMAP Derivative: Crystallographic Characterization of the Acylated Catalyst. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199939030 |
0.302 |
|
| 2010 |
Hodous BL, Ruble JC, Fu GC. ChemInform Abstract: Enantioselective Addition of Alcohols to Ketenes Catalyzed by a Planar-Chiral Azaferrocene: Catalytic Asymmetric Synthesis of Arylpropionic Acids. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199930030 |
0.383 |
|
| 2010 |
Ruble JC, Fu GC. ChemInform Abstract: Enantioselective Construction of Quaternary Stereocenters: Rearrangements of O-Acylated Azlactones Catalyzed by a Planar-Chiral Derivative of 4-(Pyrrolidino)pyridine. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199915149 |
0.326 |
|
| 2010 |
LO MM, FU GC. ChemInform Abstract: A New Class of Planar-Chiral Ligands: Synthesis of a C2-Symmetric Bisazaferrocene and Its Application in the Enantioselective Cu(I)-Catalyzed Cyclopropanation of Olefins. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199911042 |
0.334 |
|
| 2010 |
TORMO J, HAYS DS, FU GC. ChemInform Abstract: Bu3SnH-Catalyzed Reduction of Nitroalkanes to Alkanes. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199852076 |
0.386 |
|
| 2010 |
QIAO S, FU GC. ChemInform Abstract: The First Application of a Planar-Chiral Phosphorus Heterocycle in Asymmetric Catalysis: Enantioselective Hydrogenation of Dehydroamino Acids. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199845199 |
0.356 |
|
| 2010 |
LIANG J, RUBLE JC, FU GC. ChemInform Abstract: Dynamic Kinetic Resolutions Catalyzed by a Planar-Chiral Derivative of DMAP: Enantioselective Synthesis of Protected α-Amino Acids from Racemic Azlactones. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199836244 |
0.353 |
|
| 2010 |
RUBLE JC, TWEDDELL J, FU GC. ChemInform Abstract: Kinetic Resolution of Arylalkylcarbinols Catalyzed by a Planar-Chiral Derivative of DMAP: A New Benchmark for Nonenzymatic Acylation. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199833059 |
0.368 |
|
| 2010 |
DOSA PI, FU GC. ChemInform Abstract: Catalytic Asymmetric Addition of ZnPh2 to Ketones: Enantioselective Formation of Quaternary Stereocenters. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199819036 |
0.479 |
|
| 2010 |
GRUBBS RH, MILLER SJ, FU GC. ChemInform Abstract: Ring-Closing Metathesis and Related Processes in Organic Synthesis Cheminform. 27: no-no. DOI: 10.1002/chin.199612290 |
0.566 |
|
| 2010 |
SCHOLL M, LIM C, FU GC. ChemInform Abstract: Convenient and Efficient Conversion of Aldehydes to Acylated Cyanohydrins Using Tributyltin Cyanide as a Catalyst. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199606078 |
0.349 |
|
| 2010 |
FUJIMURA O, FU GC, ROTHEMUND PWK, GRUBBS RH. ChemInform Abstract: Hydroxyl-Directed, Stereoselective Olefination of Ketones by Transition Metal Alkylidenes. Cheminform. 26: no-no. DOI: 10.1002/chin.199530062 |
0.532 |
|
| 2010 |
SCHOLL M, FU GC. ChemInform Abstract: Tributyltin Cyanide Catalyzed Addition of Triethylsilyl Cyanide to Aldehydes. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199523065 |
0.458 |
|
| 2010 |
FUJIMURA O, FU GC, GRUBBS RH. ChemInform Abstract: Synthesis of Cyclic Enol Ethers via Molybdenum Alkylidene-Catalyzed Ring-Closing Metathesis. Cheminform. 26: no-no. DOI: 10.1002/chin.199504072 |
0.642 |
|
| 2010 |
HOVEYDA AH, EVANS DA, FU GC. ChemInform Abstract: Substrate-Directable Chemical Reactions Cheminform. 24: no-no. DOI: 10.1002/chin.199339345 |
0.65 |
|
| 2010 |
FU GC, GRUBBS RH. ChemInform Abstract: Synthesis of Cycloalkenes via Alkylidene-Mediated Olefin Metathesis and Carbonyl Olefination. Cheminform. 24: no-no. DOI: 10.1002/chin.199336076 |
0.664 |
|
| 2010 |
EVANS DA, FU GC, ANDERSON BA. ChemInform Abstract: Mechanistic Study of the Rhodium(I)-Catalyzed Hydroboration Reaction Cheminform. 23: no-no. DOI: 10.1002/chin.199248115 |
0.62 |
|
| 2010 |
EVANS DA, FU GC, HOVEYDA AH. ChemInform Abstract: Rhodium(I)- and Iridium(I)-Catalyzed Hydroboration Reactions: Scope and Synthetic Applications. Cheminform. 23: no-no. DOI: 10.1002/chin.199248114 |
0.709 |
|
| 2010 |
FU GC, GRUBBS RH. ChemInform Abstract: The Application of Catalytic Ring-Closing Olefin Metathesis to the Synthesis of Unsaturated Oxygen Heterocycles. Cheminform. 23: no-no. DOI: 10.1002/chin.199241134 |
0.615 |
|
| 2010 |
EVANS DA, FU GC. ChemInform Abstract: Amide-Directed, Iridium-Catalyzed Hydroboration of Olefins: Documentation of Regio- and Stereochemical Control in Cyclic and Acyclic Systems. Cheminform. 22: no-no. DOI: 10.1002/chin.199134126 |
0.549 |
|
| 2010 |
EVANS DA, FU GC. ChemInform Abstract: Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds by Catecholborane. Cheminform. 22: no-no. DOI: 10.1002/chin.199107102 |
0.482 |
|
| 2010 |
Lou S, Fu GC, Higo T, Fukuyama T. Palladium-catalyzed alkyl-alkyl suzuki cross-couplings of primary alkyl bromides at room temperature: (13-chlorotridecyloxy)triethylsilane [silane, [(13-chlorotridecyl)oxy]triethyl-] Organic Syntheses. 87: 299-309. |
0.406 |
|
| 2010 |
Lou S, Fu GC, Tsui GC, Chai DI, Lautens M. Synthesis of chiral pyridine bis(oxazoline) ligands for nickel-catalyzed asymmetric negishi cross-couplings of secondary allylic chlorides with alkylzincs: 2,6-bis[(4R)-4,5-dihydro-4-(2-phenylethyl)-2-oxazolyl]-pyridine: [Pyridine, 2,6-bis[(4R)-4,5-dihydro-4-(2-phenylethyl)-2-oxazolyl]-] Organic Syntheses. 87: 310-316. |
0.465 |
|
| 2010 |
Lou S, Fu GC, Chai DI, Tsui GC, Lautens M. Nickel-catalyzed asymmetric negishi cross-couplings of racemic secondary allylic chlorides with alkylzincs: (S,E)-ethyl 6-(1,3-dioxolan-2-YL)-4- methylhex-2-enoate: [2-Hexenoic acid, 6-(1,3-dioxolan-2-yl)-4-methyl-, ethyl ester, (2E,4S)-] Organic Syntheses. 87: 317-329. |
0.428 |
|
| 2010 |
Lou S, Fu GC, Bryan CS, Lautens M. Nickel-catalyzed enantioselective negishi cross-couplings of racemic secondary α-bromo amides with alkylzinc reagents: (S)-N-benzyl-7-cyano-2- ethyl-N-phenylheptanamide : [Heptanamide, 7-cyano-2-ethyl-N-phenyl-N- (phenylmethyl)-,(2S)-] Organic Syntheses. 87: 330-338. |
0.375 |
|
| 2009 |
Smith SW, Fu GC. Asymmetric carbon-carbon bond formation gamma to a carbonyl group: phosphine-catalyzed addition of nitromethane to allenes. Journal of the American Chemical Society. 131: 14231-3. PMID 19772285 DOI: 10.1021/Ja9061823 |
0.51 |
|
| 2009 |
Dochnahl M, Fu GC. Catalytic asymmetric cycloaddition of ketenes and nitroso compounds: enantioselective synthesis of alpha-hydroxycarboxylic acid derivatives. Angewandte Chemie (International Ed. in English). 48: 2391-3. PMID 19226588 DOI: 10.1002/Anie.200805805 |
0.452 |
|
| 2009 |
Chung YK, Fu GC. Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles. Angewandte Chemie (International Ed. in English). 48: 2225-7. PMID 19212998 DOI: 10.1002/Anie.200805377 |
0.534 |
|
| 2009 |
Lundin PM, Esquivias J, Fu GC. Catalytic asymmetric cross-couplings of racemic alpha-bromoketones with arylzinc reagents. Angewandte Chemie (International Ed. in English). 48: 154-6. PMID 19040243 DOI: 10.1002/Anie.200804888 |
0.585 |
|
| 2009 |
Lundin PM, Esquivias J, Fu GC. Nickel-Catalyzed Cross-Coupling of α-Bromoketoneswith Arylzinc Reagents Synfacts. 2009: 285-285. DOI: 10.1055/S-0028-1087782 |
0.44 |
|
| 2009 |
Lundin PM, Esquivias J, Fu GC. ChemInform Abstract: Catalytic Asymmetric Cross-Couplings of Racemic α-Bromoketones with Arylzinc Reagents. Cheminform. 40. DOI: 10.1002/CHIN.200919075 |
0.367 |
|
| 2008 |
Smith SW, Fu GC. Nickel-catalyzed Negishi cross-couplings of secondary nucleophiles with secondary propargylic electrophiles at room temperature. Angewandte Chemie (International Ed. in English). 47: 9334-6. PMID 18972493 DOI: 10.1002/Anie.200802784 |
0.591 |
|
| 2008 |
Fu GC. The development of versatile methods for palladium-catalyzed coupling reactions of aryl electrophiles through the use of P(t-Bu)3 and PCy3 as ligands. Accounts of Chemical Research. 41: 1555-64. PMID 18947239 DOI: 10.1021/Ar800148F |
0.593 |
|
| 2008 |
Smith SW, Fu GC. Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents. Journal of the American Chemical Society. 130: 12645-7. PMID 18763769 DOI: 10.1021/Ja805165Y |
0.526 |
|
| 2008 |
Berlin JM, Fu GC. Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds. Angewandte Chemie (International Ed. in English). 47: 7048-50. PMID 18668500 DOI: 10.1002/Anie.200802439 |
0.825 |
|
| 2008 |
Saito B, Fu GC. Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides. Journal of the American Chemical Society. 130: 6694-5. PMID 18447357 DOI: 10.1021/Ja8013677 |
0.569 |
|
| 2008 |
Dai X, Strotman NA, Fu GC. Catalytic asymmetric Hiyama cross-couplings of racemic alpha-bromo esters. Journal of the American Chemical Society. 130: 3302-3. PMID 18302392 DOI: 10.1021/Ja8009428 |
0.569 |
|
| 2008 |
Son S, Fu GC. Nickel-catalyzed asymmetric negishi cross-couplings of secondary allylic chlorides with alkylzincs. Journal of the American Chemical Society. 130: 2756-7. PMID 18257579 DOI: 10.1021/Ja800103Z |
0.568 |
|
| 2008 |
Smith SW, Fu GC. Nickel-Catalyzed Asymmetric Negishi Cross-Couplings Synfacts. 2008: 1304-1304. DOI: 10.1055/S-0028-1087318 |
0.466 |
|
| 2008 |
Fu G, Berlin J. Catalytic Asymmetric Synthesis of Aza-β-Lactams Synfacts. 2008: 1217-1217. DOI: 10.1055/s-0028-1083389 |
0.307 |
|
| 2008 |
Lee EC, Fu GC. ChemInform Abstract: Copper-Catalyzed Asymmetric N—H Insertion Reactons: Couplings of Diazo Compounds with Carbamates to Generate α-Amino Acids. Cheminform. 39. DOI: 10.1002/CHIN.200806172 |
0.334 |
|
| 2008 |
Fu G. ChemInform Abstract: Planar-Chiral Heterocycles as Enantioselective Organocatalysts Cheminform. 39. DOI: 10.1002/CHIN.200804248 |
0.374 |
|
| 2007 |
Lee EC, Fu GC. Copper-catalyzed asymmetric N-H insertion reactions: couplings of diazo compounds with carbamates to generate alpha-amino acids. Journal of the American Chemical Society. 129: 12066-7. PMID 17877350 DOI: 10.1021/Ja074483J |
0.562 |
|
| 2007 |
Firmansjah L, Fu GC. Intramolecular Heck reactions of unactivated alkyl halides. Journal of the American Chemical Society. 129: 11340-1. PMID 17718496 DOI: 10.1021/Ja075245R |
0.509 |
|
| 2007 |
Saito B, Fu GC. Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature. Journal of the American Chemical Society. 129: 9602-3. PMID 17628067 DOI: 10.1021/Ja074008L |
0.532 |
|
| 2007 |
Dai X, Nakai T, Romero JA, Fu GC. Enantioselective synthesis of protected amines by the catalytic asymmetric addition of hydrazoic acid to ketenes. Angewandte Chemie (International Ed. in English). 46: 4367-9. PMID 17471484 DOI: 10.1002/Anie.200700697 |
0.523 |
|
| 2007 |
Strotman NA, Sommer S, Fu GC. Hiyama reactions of activated and unactivated secondary alkyl halides catalyzed by a nickel/norephedrine complex. Angewandte Chemie (International Ed. in English). 46: 3556-8. PMID 17444579 DOI: 10.1002/Anie.200700440 |
0.47 |
|
| 2007 |
Son S, Fu GC. Copper-catalyzed asymmetric [4+1] cycloadditions of enones with diazo compounds to form dihydrofurans. Journal of the American Chemical Society. 129: 1046-7. PMID 17263382 DOI: 10.1021/Ja068344Y |
0.523 |
|
| 2007 |
Lee EC, McCauley KM, Fu GC. Catalytic asymmetric synthesis of tertiary alkyl chlorides. Angewandte Chemie (International Ed. in English). 46: 977-9. PMID 17211906 DOI: 10.1002/Anie.200604312 |
0.58 |
|
| 2007 |
Fu G, Strotman N, Sommer S. Ni-Catalyzed Coupling of Aryl Trifluorosilanes and Secondary Alkyl Halides Synfacts. 2007: 0746-0746. DOI: 10.1055/S-2007-968640 |
0.507 |
|
| 2007 |
Dai X, Nakai T, Romero JAC, Fu GC. Chiral Pyridine-Catalyzed HN3-Addition to Ketenes Synfacts. 2007: 765-765. DOI: 10.1055/S-2007-968631 |
0.452 |
|
| 2007 |
Fu G, Lee E, McCauley K. Organocatalytic Asymmetric Synthesis of Tertiary Alkyl Chlorides Synfacts. 2007: 0431-0431. DOI: 10.1055/s-2007-968347 |
0.454 |
|
| 2007 |
Wurz RP, Lee EC, Ruble JC, Fu GC. Synthesis and resolution of planar-chiral derivatives of 4- (dimethylamino)pyridine Advanced Synthesis and Catalysis. 349: 2345-2352. DOI: 10.1002/Adsc.200700219 |
0.482 |
|
| 2007 |
Dai X, Strotman NA, Fu GC. Catalytic asymmetric Hiyama cross-couplings of racemic α-bromo esters Chemtracts. 20: 456-457. |
0.37 |
|
| 2006 |
Fu GC. Applications of planar-chiral heterocycles as ligands in asymmetric catalysis. Accounts of Chemical Research. 39: 853-60. PMID 17115725 DOI: 10.1021/Ar068115G |
0.477 |
|
| 2006 |
Arp FO, Fu GC. Kinetic resolutions of indolines by a nonenzymatic acylation catalyst. Journal of the American Chemical Society. 128: 14264-5. PMID 17076493 DOI: 10.1021/Ja0657859 |
0.472 |
|
| 2006 |
Bappert E, Müller P, Fu GC. Asymmetric [3 + 2] annulations catalyzed by a planar-chiral derivative of DMAP. Chemical Communications (Cambridge, England). 2604-6. PMID 16779492 DOI: 10.1039/B603172B |
0.571 |
|
| 2006 |
González-Bobes F, Fu GC. Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids. Journal of the American Chemical Society. 128: 5360-1. PMID 16620105 DOI: 10.1021/Ja0613761 |
0.481 |
|
| 2006 |
Maier TC, Fu GC. Catalytic enantioselective O-H insertion reactions. Journal of the American Chemical Society. 128: 4594-5. PMID 16594695 DOI: 10.1021/Ja0607739 |
0.45 |
|
| 2006 |
Fischer C, Smith SW, Powell DA, Fu GC. Umpolung of Michael acceptors catalyzed by N-heterocyclic carbenes. Journal of the American Chemical Society. 128: 1472-3. PMID 16448117 DOI: 10.1021/Ja058222Q |
0.411 |
|
| 2006 |
Wilson JE, Fu GC. Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones. Angewandte Chemie (International Ed. in English). 45: 1426-9. PMID 16444787 DOI: 10.1002/Anie.200503312 |
0.514 |
|
| 2006 |
Kudo N, Perseghini M, Fu GC. A versatile method for Suzuki cross-coupling reactions of nitrogen heterocycles. Angewandte Chemie (International Ed. in English). 45: 1282-4. PMID 16425308 DOI: 10.1002/Anie.200503479 |
0.492 |
|
| 2006 |
Fu G, González-Bobes F. Nickel-Catalyzed Suzuki Reaction of Unactivated Alkyl Halides Synfacts. 2006: 0721-0721. DOI: 10.1055/s-2006-941882 |
0.432 |
|
| 2006 |
Kudo N, Perseghini M, Fu GC. A Versatile Method for Suzuki Cross-Coupling of Nitrogen Heterocycles Synfacts. 2006: 382-382. DOI: 10.1055/S-2006-934328 |
0.417 |
|
| 2006 |
Fischer C, Smith SW, Powell DA, Fu GC. Intramolecular β-Alkylation of Michael Acceptors Synfacts. 2006: 275-275. DOI: 10.1055/S-2006-931994 |
0.319 |
|
| 2006 |
Liu SY, Lo MMC, Fu GC. The synthesis of an enantiopure planar-chiral Lewis acid complex via kinetic resolution and its application in stereoselective additions to imines Tetrahedron. 62: 11343-11349. DOI: 10.1016/J.Tet.2006.06.048 |
0.624 |
|
| 2006 |
Netherton MR, Fu GC. Palladium-Catalyzed Cross-Coupling Reactions of Unactivated Alkyl Electrophiles with Organometallic Compounds Cheminform. 37. DOI: 10.1002/chin.200606260 |
0.793 |
|
| 2005 |
Liu SY, Hills ID, Fu GC. Synthesis, resolution, and aldol reactions of a planar-chiral Lewis acid complex. Journal of the American Chemical Society. 127: 15352-3. PMID 16262382 DOI: 10.1021/Ja0552702 |
0.838 |
|
| 2005 |
Wurz RP, Fu GC. Catalytic asymmetric synthesis of piperidine derivatives through the [4 + 2] annulation of imines with allenes. Journal of the American Chemical Society. 127: 12234-5. PMID 16131196 DOI: 10.1021/Ja053277D |
0.544 |
|
| 2005 |
Lee EC, Hodous BL, Bergin E, Shih C, Fu GC. Catalytic asymmetric Staudinger reactions to form beta-lactams: an unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent. Journal of the American Chemical Society. 127: 11586-7. PMID 16104719 DOI: 10.1021/Ja052058P |
0.401 |
|
| 2005 |
Suárez A, Downey CW, Fu GC. Kinetic resolutions of azomethine imines via copper-catalyzed [3 + 2] cycloadditions. Journal of the American Chemical Society. 127: 11244-5. PMID 16089444 DOI: 10.1021/Ja052876H |
0.829 |
|
| 2005 |
Arp FO, Fu GC. Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides. Journal of the American Chemical Society. 127: 10482-3. PMID 16045323 DOI: 10.1021/Ja053751F |
0.567 |
|
| 2005 |
Schaefer C, Fu GC. Catalytic asymmetric couplings of ketenes with aldehydes to generate enol esters. Angewandte Chemie (International Ed. in English). 44: 4606-8. PMID 16003799 DOI: 10.1002/Anie.200501434 |
0.544 |
|
| 2005 |
Wiskur SL, Fu GC. Catalytic asymmetric synthesis of esters from ketenes. Journal of the American Chemical Society. 127: 6176-7. PMID 15853315 DOI: 10.1021/Ja0506152 |
0.782 |
|
| 2005 |
Mermerian AH, Fu GC. Catalytic enantioselective construction of all-carbon quaternary stereocenters: synthetic and mechanistic studies of the C-acylation of silyl ketene acetals. Journal of the American Chemical Society. 127: 5604-7. PMID 15826199 DOI: 10.1021/Ja043832W |
0.544 |
|
| 2005 |
Fischer C, Fu GC. Asymmetric nickel-catalyzed Negishi cross-couplings of secondary alpha-bromo amides with organozinc reagents. Journal of the American Chemical Society. 127: 4594-5. PMID 15796523 DOI: 10.1021/Ja0506509 |
0.489 |
|
| 2005 |
Powell DA, Maki T, Fu GC. Stille cross-couplings of unactivated secondary alkyl halides using monoorganotin reagents. Journal of the American Chemical Society. 127: 510-1. PMID 15643860 DOI: 10.1021/Ja0436300 |
0.513 |
|
| 2005 |
Mermerian AH, Fu GC. Nucleophile-catalyzed asymmetric acylations of silyl ketene imines: application to the enantioselective synthesis of verapamil. Angewandte Chemie (International Ed. in English). 44: 949-52. PMID 15630710 DOI: 10.1002/Anie.200461886 |
0.56 |
|
| 2005 |
Littke AF, Fu GC. Heck reactions of aryl chlorides catalyzed by pALLADIUM/TRI-tert- butylphosphine: (E)-2-methyl-3phenylacrylic acid butyl ester and (E)-4-(2phenylethenyl)benzonitrile Organic Syntheses. 81. DOI: 10.15227/Orgsyn.081.0063 |
0.432 |
|
| 2005 |
Fu GC. Recent Advances in Rhodium(I)-Catalyzed Asymmetric Olefin Isomerization and Hydroacylation Reactions Modern Rhodium-Catalyzed Organic Reactions. 79-91. DOI: 10.1002/3527604693.ch4 |
0.412 |
|
| 2005 |
Littke AF, Fu GC. Heck Reactions of Aryl Chlorides Catalyzed by Palladium/Tri‐tert‐butylphosphine: (E)‐2‐Methyl‐3‐Phenylacrylic Acid Butyl Ester and (E)‐4‐(2‐Phenylethenyl)benzonitrile Organic Syntheses. 63-76. DOI: 10.1002/0471264229.Os081.07 |
0.476 |
|
| 2004 |
Wilson JE, Fu GC. Asymmetric synthesis of highly substituted beta-lactones by nucleophile-catalyzed [2+2] cycloadditions of disubstituted ketenes with aldehydes. Angewandte Chemie (International Ed. in English). 43: 6358-60. PMID 15558690 DOI: 10.1002/Anie.200460698 |
0.476 |
|
| 2004 |
Hills ID, Fu GC. Elucidating reactivity differences in palladium-catalyzed coupling processes: the chemistry of palladium hydrides. Journal of the American Chemical Society. 126: 13178-9. PMID 15479044 DOI: 10.1021/Ja0471424 |
0.823 |
|
| 2004 |
Fu GC. Asymmetric catalysis with "planar-chiral" derivatives of 4-(dimethylamino)pyridine. Accounts of Chemical Research. 37: 542-7. PMID 15311953 DOI: 10.1021/Ar030051B |
0.537 |
|
| 2004 |
Suárez A, Fu GC. A straightforward and mild synthesis of functionalized 3-alkynoates. Angewandte Chemie (International Ed. in English). 43: 3580-2. PMID 15293251 DOI: 10.1002/Anie.200454070 |
0.407 |
|
| 2004 |
Powell DA, Fu GC. Nickel-catalyzed cross-couplings of organosilicon reagents with unactivated secondary alkyl bromides. Journal of the American Chemical Society. 126: 7788-9. PMID 15212521 DOI: 10.1021/Ja047433C |
0.532 |
|
| 2004 |
Fu GC. From the design of a chiral Lewis acid catalyst to metal-catalyzed coupling reactions. The Journal of Organic Chemistry. 69: 3245-9. PMID 15132528 DOI: 10.1021/Jo049908O |
0.546 |
|
| 2004 |
Zhou J, Fu GC. Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides. Journal of the American Chemical Society. 126: 1340-1. PMID 14759182 DOI: 10.1021/Ja039889K |
0.559 |
|
| 2004 |
Wiskur SL, Korte A, Fu GC. Cross-couplings of alkyl electrophiles under "ligandless" conditions: Negishi reactions of organozirconium reagents. Journal of the American Chemical Society. 126: 82-3. PMID 14709070 DOI: 10.1021/Ja0393729 |
0.82 |
|
| 2004 |
Netherton MR, Fu GC. Nickel-catalyzed cross-couplings of unactivated alkyl halides and pseudohalides with organometallic compounds Advanced Synthesis and Catalysis. 346: 1525-1532. DOI: 10.1002/Adsc.200404223 |
0.809 |
|
| 2003 |
Hills ID, Netherton MR, Fu GC. Toward an improved understanding of the unusual reactivity of Pd0/trialkylphosphane catalysts in cross-couplings of alkyl electrophiles: quantifying the factors that determine the rate of oxidative addition. Angewandte Chemie (International Ed. in English). 42: 5749-52. PMID 14661214 DOI: 10.1002/Anie.200352858 |
0.804 |
|
| 2003 |
Zhou JS, Fu GC. Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides. Journal of the American Chemical Society. 125: 14726-7. PMID 14640646 DOI: 10.1021/Ja0389366 |
0.749 |
|
| 2003 |
Eckhardt M, Fu GC. The first applications of carbene ligands in cross-couplings of alkyl electrophiles: sonogashira reactions of unactivated alkyl bromides and iodides. Journal of the American Chemical Society. 125: 13642-3. PMID 14599185 DOI: 10.1021/Ja038177R |
0.557 |
|
| 2003 |
Tang H, Menzel K, Fu GC. Ligands for palladium-catalyzed cross-couplings of alkyl halides: use of an alkyldiaminophosphane expands the scope of the Stille reaction. Angewandte Chemie (International Ed. in English). 42: 5079-82. PMID 14595638 DOI: 10.1002/Anie.200352668 |
0.525 |
|
| 2003 |
Zhou J, Fu GC. Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates. Journal of the American Chemical Society. 125: 12527-30. PMID 14531697 DOI: 10.1021/Ja0363258 |
0.731 |
|
| 2003 |
Shintani R, Fu GC. Catalytic enantioselective synthesis of beta-lactams: intramolecular Kinugasa reactions and interception of an intermediate in the reaction cascade. Angewandte Chemie (International Ed. in English). 42: 4082-5. PMID 12973776 DOI: 10.1002/Anie.200352103 |
0.486 |
|
| 2003 |
Shintani R, Fu GC. A new copper-catalyzed [3 + 2] cycloaddition: enantioselective coupling of terminal alkynes with azomethine imines to generate five-membered nitrogen heterocycles. Journal of the American Chemical Society. 125: 10778-9. PMID 12952444 DOI: 10.1021/Ja036922U |
0.546 |
|
| 2003 |
Hills ID, Fu GC. Catalytic enantioselective synthesis of oxindoles and benzofuranones that bear a quaternary stereocenter. Angewandte Chemie (International Ed. in English). 42: 3921-4. PMID 12949869 DOI: 10.1002/Anie.200351666 |
0.845 |
|
| 2003 |
Tanaka K, Fu GC. Parallel kinetic resolution of 4-alkynals catalyzed by Rh(I)/Tol-BINAP: synthesis of enantioenriched cyclobutanones and cyclopentenones. Journal of the American Chemical Society. 125: 8078-9. PMID 12837058 DOI: 10.1021/Ja035489L |
0.474 |
|
| 2003 |
Lee JY, Fu GC. Room-temperature Hiyama cross-couplings of arylsilanes with alkyl bromides and iodides. Journal of the American Chemical Society. 125: 5616-7. PMID 12733884 DOI: 10.1021/Ja0349352 |
0.457 |
|
| 2003 |
Mermerian AH, Fu GC. Catalytic enantioselective synthesis of quaternary stereocenters via intermolecular C-acylation of silyl ketene acetals: dual activation of the electrophile and the nucleophile. Journal of the American Chemical Society. 125: 4050-1. PMID 12670217 DOI: 10.1021/Ja028554K |
0.533 |
|
| 2003 |
Menzel K, Fu GC. Room-temperature Stille cross-couplings of alkenyltin reagents and functionalized alkyl bromides that possess beta hydrogens. Journal of the American Chemical Society. 125: 3718-9. PMID 12656600 DOI: 10.1021/ja0344563 |
0.308 |
|
| 2003 |
Hills ID, Fu GC. Cover Picture: Catalytic Enantioselective Synthesis of Oxindoles and Benzofuranones That Bear a Quaternary Stereocenter (Angew. Chem. Int. Ed. 33/2003) Angewandte Chemie International Edition. 42: 3839-3839. DOI: 10.1002/Anie.200390555 |
0.833 |
|
| 2003 |
Hills ID, Fu GC. Titelbild: Catalytic Enantioselective Synthesis of Oxindoles and Benzofuranones That Bear a Quaternary Stereocenter (Angew. Chem. 33/2003) Angewandte Chemie. 115: 3969-3969. DOI: 10.1002/Ange.200390584 |
0.845 |
|
| 2003 |
Tormo J, Fu GC. Tributylstannane (Bu3SnH)-Catalyzed Barton-McCombie Deoxygenation of Alcohols: 3-Deoxy-1,2:5,6-Bis-O-(1-Methylethylidene)-α-D-Ribo-Hexofuranose Organic Syntheses. 239-239. DOI: 10.1002/0471264180.Os078.27 |
0.32 |
|
| 2002 |
Tanaka K, Fu GC. A novel rhodium-catalyzed reduction-oxidation process: reaction of 4-alkynals with phenol to provide cis-4-alkenoates. Angewandte Chemie (International Ed. in English). 41: 1607-9. PMID 19750681 DOI: 10.1002/1521-3773(20020503)41:9<1607::Aid-Anie1607>3.0.Co;2-Q |
0.418 |
|
| 2002 |
Kirchhoff JH, Dai C, Fu GC. Method for palladium-catalyzed cross-couplings of simple alkyl chlorides: Suzuki reactions catalyzed by [Pd2(dba)3]/PCy3. Angewandte Chemie (International Ed. in English). 41: 1945-7. PMID 19750641 |
0.388 |
|
| 2002 |
Liu SY, Lo MM, Fu GC. 1,2-azaborolyls, isoelectronic analogues of the ubiquitous cyclopentadienyl ligand: synthesis of B-heteroatom-substituted 1,2-azaborolyl complexes and an assessment of their electronic features. Angewandte Chemie (International Ed. in English). 41: 174-6. PMID 12491477 DOI: 10.1002/1521-3773(20020104)41:1<174::Aid-Anie174>3.0.Co;2-7 |
0.511 |
|
| 2002 |
Shintani R, Fu GC. Highly enantioselective desymmetrization of anhydrides by carbon nucleophiles: reactions of Grignard reagents in the presence of (-)-sparteine. Angewandte Chemie (International Ed. in English). 41: 1057-9. PMID 12491311 DOI: 10.1002/1521-3773(20020315)41:6<1057::Aid-Anie1057>3.0.Co;2-H |
0.48 |
|
| 2002 |
Littke AF, Fu GC. Palladium-catalyzed coupling reactions of aryl chlorides. Angewandte Chemie (International Ed. in English). 41: 4176-211. PMID 12434342 DOI: 10.1002/1521-3773(20021115)41:22<4176::Aid-Anie4176>3.0.Co;2-U |
0.567 |
|
| 2002 |
Kirchhoff JH, Netherton MR, Hills ID, Fu GC. Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions. Journal of the American Chemical Society. 124: 13662-3. PMID 12431081 DOI: 10.1021/Ja0283899 |
0.844 |
|
| 2002 |
Netherton MR, Fu GC. Suzuki cross-couplings of alkyl tosylates that possess beta hydrogen atoms: synthetic and mechanistic studies. Angewandte Chemie (International Ed. in English). 41: 3910-2. PMID 12386889 DOI: 10.1002/1521-3773(20021018)41:20<3910::Aid-Anie3910>3.0.Co;2-W |
0.743 |
|
| 2002 |
Tao B, Fu GC. Application of a new family of P,N ligands to the highly enantioselective hydrosilylation of aryl alkyl and dialkyl ketones. Angewandte Chemie (International Ed. in English). 41: 3892-4. PMID 12386882 DOI: 10.1002/1521-3773(20021018)41:20<3892::Aid-Anie3892>3.0.Co;2-A |
0.397 |
|
| 2002 |
Shintani R, Fu GC. Copper-catalyzed enantioselective conjugate addition of diethylzinc to acyclic enones in the presence of planar-chiral phosphaferrocene-oxazoline ligands. Organic Letters. 4: 3699-702. PMID 12375922 DOI: 10.1021/Ol026651C |
0.455 |
|
| 2002 |
Tanaka K, Fu GC. Enantioselective synthesis of cyclopentenones via rhodium-catalyzed kinetic resolution and desymmetrization of 4-alkynals. Journal of the American Chemical Society. 124: 10296-7. PMID 12197729 DOI: 10.1021/Ja0266161 |
0.534 |
|
| 2002 |
Hodous BL, Fu GC. Enantioselective addition of amines to ketenes catalyzed by a planar-chiral derivative of PPY: possible intervention of chiral Brønsted-acid catalysis. Journal of the American Chemical Society. 124: 10006-7. PMID 12188662 DOI: 10.1021/Ja027466X |
0.521 |
|
| 2002 |
Tanaka K, Fu GC. A unique rhodium-catalyzed rearrangement process: isomerization of an alkyne to a 1,3-diene with concomitant migration of a formyl group. An expeditious route to dienals from readily available 4-alkynals. Chemical Communications (Cambridge, England). 684-5. PMID 12119674 DOI: 10.1039/B200208F |
0.522 |
|
| 2002 |
Littke AF, Schwarz L, Fu GC. Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides. Journal of the American Chemical Society. 124: 6343-8. PMID 12033863 DOI: 10.1021/Ja020012F |
0.475 |
|
| 2002 |
Lo MM, Fu GC. Cu(I)/bis(azaferrocene)-catalyzed enantioselective synthesis of beta-lactams via couplings of alkynes with nitrones. Journal of the American Chemical Society. 124: 4572-3. PMID 11971699 DOI: 10.1021/Ja025833Z |
0.509 |
|
| 2002 |
Tanaka K, Fu GC. Rhodium-catalyzed synthesis of cyclohexenones via a novel [4 + 2] annulation. Organic Letters. 4: 933-5. PMID 11893189 DOI: 10.1021/Ol017308V |
0.522 |
|
| 2002 |
Hodous BL, Fu GC. Enantioselective Staudinger synthesis of beta-lactams catalyzed by a planar-chiral nucleophile. Journal of the American Chemical Society. 124: 1578-9. PMID 11853423 DOI: 10.1021/Ja012427R |
0.52 |
|
| 2002 |
Fu GC. New applications of organometallic catalysts in organic chemistry Pure and Applied Chemistry. 74: 33-36. DOI: 10.1351/Pac200274010033 |
0.585 |
|
| 2002 |
Liu S, Hills ID, Fu GC. The First General Method for the Synthesis of Transition-Metal π Complexes of an Electronically Diverse Family of 1,2-Azaborolyls Organometallics. 21: 4323-4325. DOI: 10.1021/Om020533B |
0.8 |
|
| 2002 |
Tanaka K, Fu GC. A Versatile New Method for the Synthesis of Cyclopentenones via an Unusual Rhodium-Catalyzed Intramolecular Trans Hydroacylation of an Alkyne [J. Am. Chem. Soc.2001,123, 11492−11493]. Journal of the American Chemical Society. 124: 1553-1553. DOI: 10.1021/Ja015128A |
0.472 |
|
| 2002 |
Kirchhoff JH, Dai C, Fu GC. A Method for Palladium‐Catalyzed Cross‐Couplings of Simple Alkyl Chlorides: Suzuki Reactions Catalyzed by [Pd2(dba)3]/PCy3 Angewandte Chemie. 41: 1945-1947. DOI: 10.1002/1521-3773(20020603)41:11<1945::Aid-Anie1945>3.0.Co;2-7 |
0.414 |
|
| 2001 |
Arai S, Bellemin-Laponnaz S, Fu GC. Kinetic Resolution of Amines by a Nonenzymatic Acylation Catalyst. Angewandte Chemie (International Ed. in English). 40: 234-236. PMID 29711934 DOI: 10.1002/1521-3773(20010105)40:1<234::Aid-Anie234>3.0.Co;2-K |
0.417 |
|
| 2001 |
Liu SY, Choi MJ, Fu GC. A surprisingly mild and versatile method for palladium-catalyzed Suzuki cross-couplings of aryl chlorides in the presence of a triarylphosphine. Chemical Communications (Cambridge, England). 2408-9. PMID 12239989 DOI: 10.1039/B107888G |
0.684 |
|
| 2001 |
Netherton MR, Fu GC. Air-stable trialkylphosphonium salts: simple, practical, and versatile replacements for air-sensitive trialkylphosphines. Applications in stoichiometric and catalytic processes. Organic Letters. 3: 4295-8. PMID 11784201 DOI: 10.1021/Ol016971G |
0.751 |
|
| 2001 |
Tanaka K, Fu GC. A versatile new catalyst for the enantioselective isomerization of allylic alcohols to aldehydes: scope and mechanistic studies. The Journal of Organic Chemistry. 66: 8177-86. PMID 11722222 DOI: 10.1021/Jo010792V |
0.512 |
|
| 2001 |
Tanaka K, Fu GC. A versatile new method for the synthesis of cyclopentenones via an unusual rhodium-catalyzed intramolecular trans hydroacylation of an alkyne. Journal of the American Chemical Society. 123: 11492-3. PMID 11707133 DOI: 10.1021/Ja011907F |
0.515 |
|
| 2001 |
Netherton MR, Dai C, Neuschütz K, Fu GC. Room-temperature alkyl-alkyl Suzuki cross-coupling of alkyl bromides that possess beta hydrogens. Journal of the American Chemical Society. 123: 10099-100. PMID 11592890 DOI: 10.1021/Ja011306O |
0.762 |
|
| 2001 |
Littke AF, Fu GC. A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions. Journal of the American Chemical Society. 123: 6989-7000. PMID 11459477 DOI: 10.1021/Ja010988C |
0.521 |
|
| 2001 |
Dai C, Fu GC. The first general method for palladium-catalyzed Negishi cross-coupling of aryl and vinyl chlorides: Use of commercially available Pd(P(t-Bu)3)2 as a catalyst Journal of the American Chemical Society. 123: 2719-2724. PMID 11456957 DOI: 10.1021/Ja003954Y |
0.458 |
|
| 2001 |
Tao B, Lo MM, Fu GC. Planar-chiral pyridine N-oxides, a new family of asymmetric catalysts: exploiting an eta(5)-C(5)Ar(5) ligand to achieve high enantioselectivity. Journal of the American Chemical Society. 123: 353-4. PMID 11456531 DOI: 10.1021/Ja003573K |
0.428 |
|
| 2001 |
Fu GC. Applications of "planar-chiral" heterocycles in asymmetric catalysis Pure and Applied Chemistry. 73: 1113-1116. DOI: 10.1351/Pac200173071113 |
0.577 |
|
| 2001 |
Fu GC. Asymmetric catalysis with "planar-chiral" heterocycles Pure and Applied Chemistry. 73: 347-349. DOI: 10.1351/Pac200173020347 |
0.514 |
|
| 2001 |
Bellemin-Laponnaz S, Lo MM, Peterson TH, Allen JM, Fu GC. Synthesis, Structure, and Reactivity ofC2-Symmetric Bis(phospholyl)zirconium and Bis(phospholyl)hafnium Complexes Organometallics. 20: 3453-3458. DOI: 10.1021/Om010256T |
0.423 |
|
| 2001 |
Fu GC. The chemistry of borabenzenes (1986–2000) Advances in Organometallic Chemistry. 47: 101-119. DOI: 10.1016/S0065-3055(01)47010-9 |
0.439 |
|
| 2001 |
Lo MM, Fu GC. Applications of planar-chiral heterocycles in enantioselective catalysis: Cu(I)/bisazaferrocene-catalyzed asymmetric ring expansion of oxetanes to tetrahydrofurans Tetrahedron. 57: 2621-2634. DOI: 10.1016/S0040-4020(01)00082-5 |
0.428 |
|
| 2001 |
Tao B, Lo MM, Fu GC. ChemInform Abstract: Planar-Chiral Pyridine N-Oxides, a New Family of Asymmetric Catalysts: Exploiting an η5-C5Ar5 Ligand to Achieve High Enantioselectivity. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200115037 |
0.334 |
|
| 2000 |
Shintani R, Lo MM-, Fu GC. Synthesis and application of planar-chiral phosphaferrocene-oxazolines, a new class of P,N-ligands Organic Letters. 2: 3695-3697. PMID 11073678 DOI: 10.1021/Ol006606+ |
0.48 |
|
| 2000 |
Fu GC. Enantioselective nucleophilic catalysis with 'planar-chiral' heterocycles Accounts of Chemical Research. 33: 412-420. PMID 10891059 DOI: 10.1021/Ar990077W |
0.519 |
|
| 2000 |
Hundertmark T, Littke AF, Buchwald SL, Fu GC. Pd(PhCN)(2)Cl(2)/P(t-Bu)(3): a versatile catalyst for Sonogashira reactions of aryl bromides at room temperature. Organic Letters. 2: 1729-31. PMID 10880212 DOI: 10.1021/Ol0058947 |
0.563 |
|
| 2000 |
Suginome M, Fu GC. First synthesis and resolution of a planar-chiral tetrahydroindolyl complex of iron: electronic tuning of reactivity and enantioselective nucleophilic catalysis. Chirality. 12: 318-24. PMID 10824146 DOI: 10.1002/(Sici)1520-636X(2000)12:5/6<318::Aid-Chir4>3.0.Co;2-9 |
0.375 |
|
| 2000 |
Bellemin-Laponnaz S, Tweddell J, Ruble JC, Breitling FM, Fu GC. The kinetic resolution of allylic alcohols by a non-enzymatic acylation catalyst; application to natural product synthesis Chemical Communications. 1009-1010. DOI: 10.1039/B002041I |
0.418 |
|
| 2000 |
Rios R, Liang J, Lo MM-, Fu GC. Synthesis, resolution and crystallographic characterization of a new C2-symmetric planar-chiral bipyridine ligand: application to the catalytic enantioselective cyclopropanation of olefins Chemical Communications. 377-378. DOI: 10.1039/A909457A |
0.677 |
|
| 2000 |
Ie Y, Fu GC. A new benchmark for the non-enzymatic enantioselective acylation of amines: use of a planar-chiral derivative of 4-pyrrolidinopyridine as the acylating agent Chemical Communications. 119-120. DOI: 10.1039/A908625K |
0.466 |
|
| 2000 |
Tanaka K, Qiao S, Tobisu M, Lo MM, Fu GC. Enantioselective Isomerization of Allylic Alcohols Catalyzed by a Rhodium/Phosphaferrocene Complex Journal of the American Chemical Society. 122: 9870-9871. DOI: 10.1021/Ja002471R |
0.357 |
|
| 2000 |
Littke AF, Dai C, Fu GC. Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions Journal of the American Chemical Society. 122: 4020-4028. DOI: 10.1021/Ja0002058 |
0.52 |
|
| 2000 |
Bellemin-Laponnaz S, Tweddell J, Ruble JC, Breitling FM, Fu GC. ChemInform Abstract: The Kinetic Resolution of Allylic Alcohols by a Non-enzymatic Acylation Catalyst; Application to Natural Product Synthesis. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200039029 |
0.317 |
|
| 1999 |
Littke AF, Fu GC. Heck Reactions in the Presence of P(t-Bu)(3): Expanded Scope and Milder Reaction Conditions for the Coupling of Aryl Chlorides. The Journal of Organic Chemistry. 64: 10-11. PMID 11674076 DOI: 10.1021/Jo9820059 |
0.452 |
|
| 1999 |
Littke AF, Fu GC. The First General Method for Stille Cross-Couplings of Aryl Chlorides. Angewandte Chemie. 38: 2411-2413. PMID 10458805 DOI: 10.1002/(Sici)1521-3773(19990816)38:16<2411::Aid-Anie2411>3.0.Co;2-T |
0.381 |
|
| 1999 |
Tao B, Ruble JC, Hoic DA, Fu GC. Nonenzymatic Kinetic Resolution of Propargylic Alcohols by a Planar−Chiral DMAP Derivative: Crystallographic Characterization of the Acylated Catalyst [J. Am. Chem. Soc.1999,121, 5091−5092]. Journal of the American Chemical Society. 121: 10452-10452. DOI: 10.1021/Ja995532Y |
0.365 |
|
| 1999 |
Tao B, Ruble JC, Hoic DA, Fu GC. Nonenzymatic Kinetic Resolution of Propargylic Alcohols by a Planar−Chiral DMAP Derivative: Crystallographic Characterization of the Acylated Catalyst Journal of the American Chemical Society. 121: 5091-5092. DOI: 10.1021/Ja9906958 |
0.367 |
|
| 1999 |
Hodous BL, Ruble JC, Fu GC. Enantioselective Addition of Alcohols to Ketenes Catalyzed by a Planar-Chiral Azaferrocene: Catalytic Asymmetric Synthesis of Arylpropionic Acids Journal of the American Chemical Society. 121: 2637-2638. DOI: 10.1021/Ja984021T |
0.477 |
|
| 1999 |
Hays DS, Fu GC. The development of a new catalytic process: Bu3SnH-catalyzed reductive cyclization of enals and enones Tetrahedron. 55: 8815-8832. DOI: 10.1016/S0040-4020(99)00446-9 |
0.542 |
|
| 1998 |
Littke AF, Fu GC. A Convenient and General Method for Pd-Catalyzed Suzuki Cross-Couplings of Aryl Chlorides and Arylboronic Acids. Angewandte Chemie (International Ed. in English). 37: 3387-3388. PMID 29711304 DOI: 10.1002/(Sici)1521-3773(19981231)37:24<3387::Aid-Anie3387>3.0.Co;2-P |
0.484 |
|
| 1998 |
Tormo J, Hays DS, Fu GC. Diastereoselective Synthesis of beta-Amino Alcohols via Bu(3)SnH-Mediated Reductive Cyclization of Carbonyl-Oxime Ethers. The Journal of Organic Chemistry. 63: 201-202. PMID 11674066 DOI: 10.1021/Jo971574Y |
0.366 |
|
| 1998 |
Hays DS, Fu GC. Bu(3)SnH-Mediated Pinacol Coupling of 1,5- and 1,6-Dicarbonyl Compounds: Synthetic and Mechanistic Studies. The Journal of Organic Chemistry. 63: 6375-6381. PMID 11672272 DOI: 10.1021/Jo9809130 |
0.525 |
|
| 1998 |
Qiao S, Hoic DA, Fu GC. Synthesis, Resolution, and Crystallographic Characterization of aC2-Symmetric Diphosphaferrocene Organometallics. 17: 773-774. DOI: 10.1021/Om970845S |
0.371 |
|
| 1998 |
Tormo J, Hays DS, Fu GC. Bu3SnH-Catalyzed Reduction of Nitroalkanes to Alkanes The Journal of Organic Chemistry. 63: 5296-5297. DOI: 10.1021/Jo980789K |
0.505 |
|
| 1998 |
Qiao S, Fu GC. The First Application of a Planar-Chiral Phosphorus Heterocycle in Asymmetric Catalysis: Enantioselective Hydrogenation of Dehydroamino Acids The Journal of Organic Chemistry. 63: 4168-4169. DOI: 10.1021/Jo980624B |
0.454 |
|
| 1998 |
Liang J, Ruble JC, Fu GC. Dynamic Kinetic Resolutions Catalyzed by a Planar-Chiral Derivative of DMAP: Enantioselective Synthesis of Protected α-Amino Acids from Racemic Azlactones The Journal of Organic Chemistry. 63: 3154-3155. DOI: 10.1021/Jo9803380 |
0.455 |
|
| 1998 |
Ruble JC, Tweddell J, Fu GC. Kinetic Resolution of Arylalkylcarbinols Catalyzed by a Planar-Chiral Derivative of DMAP: A New Benchmark for Nonenzymatic Acylation The Journal of Organic Chemistry. 63: 2794-2795. DOI: 10.1021/Jo980183W |
0.466 |
|
| 1998 |
Hays DS, Fu GC. Development of Bu3SnH-Catalyzed Processes: Efficient Reduction of Azides to Amines The Journal of Organic Chemistry. 63: 2796-2797. DOI: 10.1021/Jo9721958 |
0.428 |
|
| 1998 |
Garrett CE, Fu GC. Exploiting η5- to η3-Indenyl Ring Slippage to Access a Directed Reaction: Ether-Directed, Rhodium-Catalyzed Olefin Hydroboration The Journal of Organic Chemistry. 63: 1370-1371. DOI: 10.1021/Jo9720647 |
0.486 |
|
| 1998 |
Garrett CE, Fu GC. Nucleophilic Catalysis with π-Bound Nitrogen Heterocycles: Synthesis of the First Ruthenium Catalysts and Comparison of the Reactivity and the Enantioselectivity of Ruthenium and Iron ComplexesJ. Am. Chem. Soc.1998,120, 7479−7483 Journal of the American Chemical Society. 120: 10276-10276. DOI: 10.1021/Ja985520X |
0.469 |
|
| 1998 |
Ruble JC, Fu GC. Enantioselective Construction of Quaternary Stereocenters: Rearrangements ofO-Acylated Azlactones Catalyzed by a Planar-Chiral Derivative of 4-(Pyrrolidino)pyridine Journal of the American Chemical Society. 120: 11532-11533. DOI: 10.1021/Ja982890C |
0.523 |
|
| 1998 |
Lo MM, Fu GC. A New Class of Planar−Chiral Ligands: Synthesis of aC2-Symmetric Bisazaferrocene and Its Application in the Enantioselective Cu(I)-Catalyzed Cyclopropanation of Olefins Journal of the American Chemical Society. 120: 10270-10271. DOI: 10.1021/Ja982488Y |
0.406 |
|
| 1998 |
Garrett CE, Fu GC. Nucleophilic catalysis with π-bound nitrogen heterocycles: Synthesis of the first ruthenium catalysts and comparison of the reactivity and the enantioselectivity of ruthenium and iron complexes Journal of the American Chemical Society. 120: 7479-7483. DOI: 10.1021/Ja981061O |
0.464 |
|
| 1998 |
Dosa PI, Fu GC. Catalytic asymmetric addition of ZnPh2 to ketones: Enantioselective formation of quaternary stereocenters Journal of the American Chemical Society. 120: 445-446. DOI: 10.1021/Ja973169U |
0.567 |
|
| 1997 |
Tweddell J, Hoic DA, Fu GC. First Synthesis and Structural Characterization of an Enantiomerically Pure Planar-Chiral Lewis Acid Complex. The Journal of Organic Chemistry. 62: 8286-8287. PMID 11671960 DOI: 10.1021/Jo971757K |
0.423 |
|
| 1997 |
Hays DS, Fu GC. A New Method for Generating Sn-H Bonds: Reactions of Tin Amides with Silicon Hydrides. The Journal of Organic Chemistry. 62: 7070-7071. PMID 11671797 DOI: 10.1021/Jo9710700 |
0.369 |
|
| 1997 |
Garrett CE, Fu GC. pi-Bound Phosphorus Heterocycles as Catalysts: Ring Opening of Epoxides with TMSCl in the Presence of a Phosphaferrocene. The Journal of Organic Chemistry. 62: 4534-4535. PMID 11671791 DOI: 10.1021/Jo970419G |
0.443 |
|
| 1997 |
Dosa PI, Ruble JC, Fu GC. Planar-Chiral Heterocycles as Ligands in Metal-Catalyzed Processes: Enantioselective Addition of Organozinc Reagents to Aldehydes. The Journal of Organic Chemistry. 62: 444-445. PMID 11671428 |
0.356 |
|
| 1997 |
Qiao S, Hoic DA, Fu GC. Synthesis and Structure of Borabenzene−4-Phenylpyridine, a Heterocyclic Analogue ofp-Terphenyl Organometallics. 16: 1501-1502. DOI: 10.1021/Om9608869 |
0.341 |
|
| 1997 |
Lopez RM, Fu GC. A mild, convenient, and inexpensive method for converting imines into amines: Tin-catalyzed reduction with polymethylhydrosiloxane (PMHS) Tetrahedron. 53: 16349-16354. DOI: 10.1016/S0040-4020(97)01020-X |
0.511 |
|
| 1997 |
Amendola MC, Stockman KE, Hoic DA, Davis WM, Fu GC. Defining the Conformation of Lewis Acid/Lewis Base Complex: Crystallographic Evidence for Simultaneousσ andπ Donation by a Carbonyl Group to a Divalent Boron Lewis Acid Angewandte Chemie International Edition in English. 36: 267-269. DOI: 10.1002/Anie.199702671 |
0.321 |
|
| 1996 |
Ruble JC, Fu GC. Chiral pi-Complexes of Heterocycles with Transition Metals: A Versatile New Family of Nucleophilic Catalysts. The Journal of Organic Chemistry. 61: 7230-7231. PMID 11667636 |
0.303 |
|
| 1996 |
Hays DS, Scholl M, Fu GC. Organotin Hydride-Catalyzed Conjugate Reduction of alpha,beta-Unsaturated Ketones. The Journal of Organic Chemistry. 61: 6751-6752. PMID 11667556 DOI: 10.1021/Jo960846E |
0.678 |
|
| 1996 |
Hoic DA, Wolf JR, Davis WM, Fu GC. Chemistry of Borabenzene: Efficient and General Synthesis of New Neutral Borabenzene−Ligand Complexes Organometallics. 15: 1315-1318. DOI: 10.1021/Om9505569 |
0.353 |
|
| 1996 |
Hays DS, Fu GC. Organotin Hydride Catalyzed Carbon−Carbon Bond Formation: Radical-Mediated Reductive Cyclization of Enals and Enones The Journal of Organic Chemistry. 61: 4-5. DOI: 10.1021/Jo951827S |
0.403 |
|
| 1996 |
Hoic DA, Davis WM, Fu GC. Diphenylphosphidoboratabenzene: An Anionic Analogue of Triphenylphosphine Journal of the American Chemical Society. 118: 8176-8177. DOI: 10.1021/Ja9615740 |
0.306 |
|
| 1996 |
Qiao S, Hoic DA, Fu GC. Nucleophilic aromatic substitution reactions of borabenzene-trimethylphosphine: A versatile route to 1-substituted boratabenzenes Journal of the American Chemical Society. 118: 6329-6330. DOI: 10.1021/Ja960938L |
0.492 |
|
| 1995 |
Scholl M, Lim C, Fu GC. Convenient and efficient conversion of aldehydes to acylated cyanohydrins using tributyltin cyanide as catalyst The Journal of Organic Chemistry. 60: 6229-6231. DOI: 10.1021/Jo00124A052 |
0.735 |
|
| 1995 |
Hays DS, Fu GC. Metal Hydride Mediated Intramolecular Pinacol Coupling of Dialdehydes and Ketoaldehydes Journal of the American Chemical Society. 117: 7283-7284. DOI: 10.1021/Ja00132A044 |
0.361 |
|
| 1995 |
Fujimura O, Fu GC, Rothemund PWK, Grubbs RH. Hydroxyl-Directed, Stereoselective Olefination of Ketones by Transition Metal Alkylidenes Journal of the American Chemical Society. 117: 2355-2356. DOI: 10.1021/Ja00113A027 |
0.571 |
|
| 1995 |
Grubbs RH, Miller SJ, Fu GC. Ring-Closing Metathesis and Related Processes in Organic Synthesis Accounts of Chemical Research. 28: 446-452. DOI: 10.1021/Ar00059A002 |
0.748 |
|
| 1994 |
Scholl M, Fu GC. Tributyltin Cyanide-Catalyzed Addition of Triethylsilyl Cyanide to Aldehydes The Journal of Organic Chemistry. 59: 7178-7179. DOI: 10.1021/Jo00102A058 |
0.799 |
|
| 1994 |
Fujimura O, Fu GC, Grubbs RH. The Synthesis of Cyclic Enol Ethers via Molybdenum Alkylidene-Catalyzed Ring-Closing Metathesis The Journal of Organic Chemistry. 59: 4029-4031. DOI: 10.1021/Jo00094A002 |
0.689 |
|
| 1993 |
Fu GC, Nguyen ST, Grubbs RH. Catalytic ring-closing metathesis of functionalized dienes by a ruthenium carbene complex Journal of the American Chemical Society. 115: 9856-9857. DOI: 10.1021/Ja00074A085 |
0.696 |
|
| 1993 |
Fu GC, Grubbs RH. Synthesis of cycloalkenes via alkylidene-mediated olefin metathesis and carbonyl olefination Journal of the American Chemical Society. 115: 3800-3801. DOI: 10.1021/Ja00062A066 |
0.697 |
|
| 1993 |
Hoveyda AH, Evans DA, Fu GC. Substrate-directable chemical reactions Chemical Reviews. 93: 1307-1370. DOI: 10.1021/Cr00020A002 |
0.67 |
|
| 1992 |
Fu GC, Grubbs RH. The synthesis of nitrogen heterocycles via catalytic ring-closing metathesis of dienes Journal of the American Chemical Society. 114: 7324-7325. DOI: 10.1021/Ja00044A070 |
0.678 |
|
| 1992 |
Evans DA, Fu GC, Anderson BA. Mechanistic study of the rhodium(I)-catalyzed hydroboration reaction Journal of the American Chemical Society. 114: 6679-6685. DOI: 10.1021/Ja00043A010 |
0.659 |
|
| 1992 |
Evans DA, Fu GC, Hoveyda AH. Rhodium(I)- and iridium(I)-catalyzed hydroboration reactions: scope and synthetic applications Journal of the American Chemical Society. 114: 6671-6679. DOI: 10.1021/Ja00043A009 |
0.752 |
|
| 1992 |
Fu GC, Grubbs RH. The application of catalytic ring-closing olefin metathesis to the synthesis of unsaturated oxygen heterocycles Journal of the American Chemical Society. 114: 5426-5427. DOI: 10.1021/Ja00039A065 |
0.65 |
|
| 1992 |
FU GC, GRUBBS RH. ChemInform Abstract: Synthesis of Nitrogen Heterocycles via Catalytic Ring-Closing Metathesis of Dienes. Cheminform. 23: no-no. DOI: 10.1002/chin.199251089 |
0.646 |
|
| 1991 |
Evans DA, Fu GC. Amide-directed, iridium-catalyzed hydroboration of olefins: documentation of regio- and stereochemical control in cyclic and acyclic systems Journal of the American Chemical Society. 113: 4042-4043. DOI: 10.1021/Ja00010A083 |
0.674 |
|
| 1990 |
Evans DA, Fu GC. Conjugate reduction of .alpha.,.beta.-unsaturated carbonyl compounds by catecholborane The Journal of Organic Chemistry. 55: 5678-5680. DOI: 10.1021/Jo00309A007 |
0.603 |
|
| 1990 |
Evans DA, Fu GC. The rhodium-catalyzed hydroboration of olefins: a mechanistic investigation The Journal of Organic Chemistry. 55: 2280-2282. DOI: 10.1021/Jo00295A007 |
0.701 |
|
| 1989 |
EVANS DA, FU GC, HOVEYDA AH. ChemInform Abstract: Rhodium(I)-Catalyzed Hydroboration of Olefins. The Documentation of Regio- and Stereochemical Control in Cyclic and Acyclic Systems. Cheminform. 20. DOI: 10.1002/chin.198902107 |
0.645 |
|
| 1988 |
Evans DA, Fu GC, Hoveyda AH. Rhodium(I)-catalyzed hydroboration of olefins. The documentation of regio- and stereochemical control in cyclic and acyclic systems Journal of the American Chemical Society. 110: 6917-6918. DOI: 10.1021/Ja00228A068 |
0.653 |
|
| 1986 |
Hawkins JM, Fu GC. Asymmetric Michael reactions of 3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepine with methyl crotonate The Journal of Organic Chemistry. 51: 2820-2822. DOI: 10.1021/Jo00364A041 |
0.301 |
|
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