Gregory C. Fu, Ph.D. - Publications

Affiliations: 
1993-2012 Chemistry Massachusetts Institute of Technology, Cambridge, MA, United States 
 2012- Chemistry California Institute of Technology, Pasadena, CA 
Area:
Catalysis, enantioselective synthesis, mechanistic studies, organic chemistry, organometallic chemistry, reaction development
Website:
http://www.cce.caltech.edu/content/gregory-c-fu

162 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  1
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  0.8
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  0.64
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  1
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  0.92
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  0.64
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  0.8
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  0.64
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  0.64
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  0.8
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  0.56
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  1
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  0.64
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  0.56
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  0.76
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  0.76
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  1
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  1
2016 Fu GC, Yang ZD, Zhou SY, Yu HT, Zhang F, Yao XJ. Two new compounds, deacetylisowortmins A and B, isolated from an endophytic Fungus, Talaromyces wortmannii LGT-4. Natural Product Research. 1-5. PMID 26729481 DOI: 10.1080/14786419.2015.1129329  0.64
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  1
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  1
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  1
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  1
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  1
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  1
2015 Wan B, Fu GC. Method of reliability computer simulation assessment for microelectronic device under multi-failure mechanism Computing, Control, Information and Education Engineering - Proceedings of the 2015 2nd International Conference On Computer, Intelligent and Education Technology, Cicet 2015. 985-988.  0.56
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2014 Wan B, Fu GC, Dong YB. Solving the lower reliability confidence limit of binomial distribution by using numeric iteration method Advanced Materials Research. 842: 764-767. DOI: 10.4028/www.scientific.net/AMR.842.764  0.88
2014 Li Y, Fu GC, Li N. Thermal design improvements on avionic device in confined space under supersonic conditions Advanced Materials Research. 842: 536-540. DOI: 10.4028/www.scientific.net/AMR.842.536  0.88
2014 Li Q, Fu GC, Wan B. Study of adhesive curing pressure in process of ferrite phase shifter Advanced Materials Research. 842: 271-274. DOI: 10.4028/www.scientific.net/AMR.842.271  0.88
2014 Wu ZX, Fu GC, Gu HT. Electro-thermal effect analysis on GaAs PHEMT based on physical model Advanced Materials Research. 842: 192-195. DOI: 10.4028/www.scientific.net/AMR.842.192  0.88
2014 Su YT, Fu GC, Gu HT, Jia MS. Thermal cyclic test safety and effectiveness analysis method for astronautic electronic products based on thermal simulation Applied Mechanics and Materials. 568: 1698-1701. DOI: 10.4028/www.scientific.net/AMM.568-570.1698  0.88
2014 Fu GC, Tang M, Lu JQ, Mao JF. Thermal sensitivity analysis of on-chip interconnects Electronics Letters. 50: 797-799. DOI: 10.1049/el.2014.0517  0.56
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2012 Hu WJ, Fu GC, Xu XG, Zhu FM, Lv HJ, Yan LX. [Study on a novel mutation of B glycosyltransferase gene related with an ABx variant]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 29: 566-9. PMID 23042395 DOI: 10.3760/cma.j.issn.1003-9406.2012.05.014  0.68
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2012 Fu GC, Lin WC. Identification of gene-oriented exon orthology between human and mouse. Bmc Genomics. 13: S10. PMID 22369432 DOI: 10.1186/1471-2164-13-S1-S10  0.6
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  1
2012 Jiang M, Gao C, Huang JY, Fu GC, Cheng Y. A new method for calculating the copper coverage of PCB Advanced Materials Research. 462: 129-134. DOI: 10.4028/www.scientific.net/AMR.462.129  0.88
2012 Fu GC. Foreword Pauson-Khand Reaction: Scope, Variations and Applications. xiii. DOI: 10.1002/9781119941934  1
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  1
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  1
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  1
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  1
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  1
2011 Chen J, Qiao J, Liu HL, Yin WY, Fu GC, Zhang QF. A facile approach to polymer/clay nanocomposite by in situ redox polymerization Current Nanoscience. 7: 552-555. DOI: 10.2174/157341311796196817  0.36
2011 Li XM, Liang B, Zhang MC, Fu GC. Research on digital electronics teaching Communications in Computer and Information Science. 244: 515-521. DOI: 10.1007/978-3-642-27452-7_70  0.72
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  0.76
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  0.76
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  0.76
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  0.76
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  1
2010 Jin XD, Fu GC, Xu XG, Zhu FM, Yan LX. [Molecular basis for real RhD negative and RhDel phenotypes in Yiwu population of Zhejiang Province in China]. Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo Bing Li Sheng Li Xue Hui = Journal of Experimental Hematology / Chinese Association of Pathophysiology. 18: 1051-4. PMID 20723327  0.68
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2010 Marion N, Fu GC. Applications of Aza- and Phosphaferrocenes and Related Compounds in Asymmetric Catalysis Chiral Ferrocenes in Asymmetric Catalysis: Synthesis and Applications. 307-335. DOI: 10.1002/9783527628841.ch11  1
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.  1
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.  1
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.  1
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.  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2007 Dai X, Strotman NA, Fu GC. Catalytic asymmetric Hiyama cross-couplings of racemic α-bromo esters Chemtracts. 20: 456-457.  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2006 Zhang D, Fu GC. Study of compact thermal models for electronic packages Dianzi Qijian/Journal of Electron Devices. 29: 672-675+679.  0.64
2006 Fu GC, Wang W, Jiang TM. Studies on the application of genetic algorithm in optimal design for heat sinks Dianzi Qijian/Journal of Electron Devices. 29: 110-113.  0.64
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2005 Fu GC, Dong C, Li MX, Guo J, Yang LH. Structural, transport and magnetic properties of K xCoO 2 (x = 0.36) Chinese Physics Letters. 22: 1478-1480. DOI: 10.1088/0256-307X/22/6/050  0.84
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  1
2005 Fu GC, Li MX, Dong C, Guo J, Yang LH. Structural, transport and magnetic properties of KxCoO2·yH2O(x < 0.2, y ≤ 0.8) Wuli Xuebao/Acta Physica Sinica. 54: 5713-5716.  0.84
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.  1
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  1
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  1
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  1
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  1
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  1
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  0.8
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  1
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  1
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  0.92
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  0.8
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  0.8
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  0.88
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  0.32
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  0.76
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  0.84
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  0.92
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  0.92
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  1
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  0.32
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  0.6
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  0.32
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  0.84
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  0.92
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  0.92
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  0.48
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  0.48
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  0.48
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  0.4
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  0.4
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  0.48
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