Fu, Gregory

Article from CaltechAUTHORS

• Hossain, Asik and Anderson, Robert L., et el. (2024) Nickel-Catalyzed Enantioconvergent and Diastereoselective Allenylation of Alkyl Electrophiles: Simultaneous Control of Central and Axial Chirality; Journal of the American Chemical Society; Vol. 146; No. 11; 7173-7177; PMCID PMC11003353; 10.1021/jacs.4c00593
• Wang, Zhuo-Yan and Freas, Dylan J., et el. (2023) Phosphine Catalysis of the Fluorination of Unactivated Tertiary Alkyl Chlorides under Mild and Convenient Conditions; Journal of the American Chemical Society; Vol. 145; No. 46; 25093-25097; PMCID PMC10942731; 10.1021/jacs.3c11042
• Tong, Xiaoyu and Yang, Ze‐Peng, et el. (2023) Iron‐Catalyzed Reductive Cross‐Coupling of Alkyl Electrophiles with Olefins; Angewandte Chemie International Edition; Art. No. e202306663; PMCID PMC10528270; 10.1002/anie.202306663
• Chen, Caiyou and Fu, Gregory C. (2023) Copper-catalysed enantioconvergent alkylation of oxygen nucleophiles; Nature; Vol. 618; No. 7964; 301-307; PMCID PMC10986234; 10.1038/s41586-023-06001-y
• Zuccarello, Giuseppe and Batiste, Suzanne M., et el. (2023) Enantioselective Synthesis of α-Aminoboronic Acid Derivatives via Copper-Catalyzed N-Alkylation; Journal of the American Chemical Society; Vol. 145; No. 6; 3330-3334; PMCID PMC10079214; 10.1021/jacs.3c00038
• Tong, Xiaoyu and Schneck, Felix, et el. (2022) Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles; Journal of the American Chemical Society; Vol. 144; No. 32; 14856-14863; PMCID PMC10079215; 10.1021/jacs.2c06154
• Cho, Hyungdo and Suematsu, Hidehiro, et el. (2022) Photoinduced, Copper-Catalyzed Enantioconvergent Alkylations of Anilines by Racemic Tertiary Electrophiles: Synthesis and Mechanism; Journal of the American Chemical Society; Vol. 144; No. 10; 4550-4558; PMCID PMC9239302; 10.1021/jacs.1c12749
• Lee, Heejun and Ahn, Jun Myun, et el. (2022) 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; Vol. 144; No. 9; 4114-4123; PMCID PMC9269863; 10.1021/jacs.1c13151
• Chen, Caiyou and Peters, Jonas C., et el. (2021) Photoinduced copper-catalysed asymmetric amidation via ligand cooperativity; Nature; Vol. 596; No. 7871; 250-256; PMCID PMC8363576; 10.1038/s41586-021-03730-w
• Yang, Ze-Peng and Freas, Dylan J., et el. (2021) Asymmetric Synthesis of Protected Unnatural α-Amino Acids via Enantioconvergent Nickel-Catalyzed Cross-Coupling; Journal of the American Chemical Society; Vol. 143; No. 23; 8614-8618; PMCID PMC8351905; 10.1021/jacs.1c03903
• Wang, Zhaobin and Yang, Ze-Peng, et el. (2021) Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides; Nature Chemistry; Vol. 13; No. 3; 236-242; 10.1038/s41557-020-00609-7
• Yang, Ze-Peng and Freas, Dylan J., et el. (2021) The Asymmetric Synthesis of Amines via Nickel-Catalyzed Enantioconvergent Substitution Reactions; Journal of the American Chemical Society; Vol. 143; No. 7; 2930-2937; PMCID PMC8336453; 10.1021/jacs.0c13034
• Yang, Ze-Peng and Fu, Gregory C. (2020) Convergent Catalytic Asymmetric Synthesis of Esters of Chiral Dialkyl Carbinols; Journal of the American Chemical Society; Vol. 142; No. 12; 5870-5875; PMCID PMC7580270; 10.1021/jacs.0c01324
• Huo, Haohua and Gorsline, Bradley J., et el. (2020) Catalyst-controlled doubly enantioconvergent coupling of racemic alkyl nucleophiles and electrophiles; Science; Vol. 367; No. 6477; 559-564; PMCID PMC7566878; 10.1126/science.aaz3855
• Yin, Haolin and Fu, Gregory C. (2019) Mechanistic Investigation of Enantioconvergent Kumada Reactions of Racemic α-Bromoketones Catalyzed by a Nickel/Bis(oxazoline) Complex; Journal of the American Chemical Society; Vol. 141; No. 38; 15433-15440; PMCID PMC7075318; 10.1021/jacs.9b08185
• Bartoszewicz, Agnieszka and Matier, Carson D., et el. (2019) Enantioconvergent Alkylations of Amines by Alkyl Electrophiles: Copper-Catalyzed Nucleophilic Substitutions of Racemic α-Halolactams by Indoles; Journal of the American Chemical Society; Vol. 141; No. 37; 14864-14869; PMCID PMC7055584; 10.1021/jacs.9b07875
• Masuda, Yusuke and Fu, Gregory C. (2019) Synthesis of Chiral Diamine Ligands for Nickel-catalyzed Asymmetric Cross-couplings of Alkylchloroboronate Esters with Alkylzincs: (1R,2R)-N,N'-Dimethyl-1,2-bis(2-methylphenyl)-1,2-diaminoethane; Organic Syntheses; Vol. 96; 245-257; PMCID PMC7064032; 10.15227/orgsyn.096.0245
• Fu, Gregory C. (2019) Enantioconvergent Cross−Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes; Angewandte Chemie International Edition; Vol. 58; No. 11; 3571-3574; PMCID PMC6399024; 10.1002/anie.201814208
• He, Jian and Chen, Caiyou, et el. (2018) Visible-Light-Induced, Copper-Catalyzed Three-Component Coupling of Alkyl Halides, Olefins, and Trifluoromethylthiolate to Generate Trifluoromethyl Thioethers; ACS Catalysis; Vol. 8; No. 12; 11741-11748; PMCID PMC6687088; 10.1021/acscatal.8b04094
• Wang, Zhaobin and Yin, Haolin, et el. (2018) Catalytic Enantioconvergent Couplings of Secondary and Tertiary Electrophiles with Olefins; Nature; Vol. 563; No. 7731; 379-383; PMCID PMC6296363; 10.1038/s41586-018-0669-y
• Wang, Zhaobin and Bachman, Shoshana, et el. (2018) Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles; Angewandte Chemie International Edition; Vol. 57; No. 44; 14529-14532; PMCID PMC6200647; 10.1002/anie.201806015
• Ahn, Jun Myun and Peters, Jonas C., et el. (2017) 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; Vol. 139; No. 49; 18101-18106; PMCID PMC6039098; 10.1021/jacs.7b10907
• Matier, Carson D. and Schwaben, Jonas, et el. (2017) Copper-Catalyzed Alkylation of Aliphatic Amines Induced by Visible Light; Journal of the American Chemical Society; Vol. 139; No. 49; 17707-17710; PMCID PMC6044445; 10.1021/jacs.7b09582
• Ahn, Jun Myun and Ratani, Tanvi S., et el. (2017) Photoinduced, Copper-Catalyzed Alkylation of Amines: A Mechanistic Study of the Cross-Coupling of Carbazole with Alkyl Bromides; Journal of the American Chemical Society; Vol. 139; No. 36; 12716-12723; PMCID PMC5685493; 10.1021/jacs.7b07052
• Zhao, Wei and Wurz, Ryan P., et el. (2017) Photoinduced, Copper-Catalyzed Decarboxylative C–N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement; Journal of the American Chemical Society; Vol. 139; No. 35; 12153-12156; PMCID PMC5624330; 10.1021/jacs.7b07546
• Fu, Gregory C. (2017) Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to S_N1 and S_N2 Processes; ACS Central Science; Vol. 3; No. 7; 692-700; PMCID PMC5532721; 10.1021/acscentsci.7b00212
• Mu, Xin and Shibata, Yu, et el. (2017) Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling; Angewandte Chemie International Edition; Vol. 56; No. 21; 5821-5824; PMCID PMC5595219; 10.1002/anie.201702402
• Choi, Junwon and Fu, Gregory C. (2017) Transition metal–catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry; Science; Vol. 356; No. 6334; Art. No. eaaf7230; PMCID PMC5611817; 10.1126/science.aaf7230
• Kalek, Marcin and Fu, Gregory C. (2017) 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; Vol. 139; No. 11; 4225-4229; PMCID PMC5486213; 10.1021/jacs.7b01826
• Schmidt, Jens and Choi, Junwon, et el. (2016) A general, modular method for the catalytic asymmetric synthesis of alkylboronate esters; Science; Vol. 354; No. 6317; 1265-1269; PMCID PMC5619240; 10.1126/science.aai8611
• Ziegler, Daniel T. and Fu, Gregory C. (2016) 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; Vol. 138; No. 37; 12069-12072; PMCID PMC5065328; 10.1021/jacs.6b08486
• Chu, Crystal K. and Liang, Yufan, et el. (2016) 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; Vol. 138; No. 20; 6404-6407; PMCID PMC5031417; 10.1021/jacs.6b03465
• Johnson, Miles W. and Hannoun, Kareem I., et el. (2016) A mechanistic investigation of the photoinduced, copper-mediated cross-coupling of an aryl thiol with an aryl halide; Chemical Science; Vol. 7; 4091-4100; PMCID PMC5201211; 10.1039/c5sc04709a
• Kainz, Quirin M. and Matier, Carson D., et el. (2016) Asymmetric copper-catalyzed C-N cross-couplings induced by visible light; Science; Vol. 351; No. 6274; 681-684; PMCID PMC4770572; 10.1126/science.aad8313
• Zuo, Zhiwei and Cong, Huan, et el. (2016) Enantioselective Decarboxylative Arylation of α-Amino Acids via the Merger of Photoredox and Nickel Catalysis; Journal of the American Chemical Society; Vol. 138; No. 6; 1832-1835; PMCID PMC4862596; 10.1021/jacs.5b13211
• Ratani, Tanvi S. and Bachman, Shoshana, et el. (2015) 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; Vol. 137; No. 43; 13902-13907; PMCID PMC4666296; 10.1021/jacs.5b08452
• Liang, Yufan and Fu, Gregory C. (2015) Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF_3 and an Alkyl Group; Journal of the American Chemical Society; Vol. 137; No. 30; 9523-9526; PMCID PMC4610818; 10.1021/jacs.5b04725
• Kalek, Marcin and Fu, Gregory C. (2015) 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; Vol. 137; No. 29; 9438-9442; PMCID PMC4577964; 10.1021/jacs.5b05528
• Liang, Yufan and Fu, Gregory C. (2015) 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 Edition; Vol. 54; No. 31; 9047-9051; PMCID PMC4521909; 10.1002/anie.201503297
• Lee, Sarah Yunmi and Fujiwara, Yuji, et el. (2015) Phosphine-Catalyzed Enantioselective Intramolecular [3+2] Annulations To Generate Fused Ring Systems; Journal of the American Chemical Society; Vol. 137; No. 13; 4587-4591; PMCID PMC4433041; 10.1021/jacs.5b01985
• Kramer, Søren and Fu, Gregory C. (2015) 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; Vol. 137; No. 11; 3803-3806; PMCID PMC4433051; 10.1021/jacs.5b01944
• Fu, Gregory C. (2015) Photoinduced, copper-catalyzed coupling reaction; Abstracts of Papers of the American Chemical Society; Vol. 249; BMGT-9
• Schley, Nathan D. and Fu, Gregory C. (2014) Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation; Journal of the American Chemical Society; Vol. 136; No. 47; 16588-16593; PMCID PMC4277758; 10.1021/ja508718m
• Ziegler, Daniel T. and Riesgo, Lorena, et el. (2014) Biphenyl-Derived Phosphepines as Chiral Nucleophilic Catalysts: Enantioselective [4+1] Annulations To Form Functionalized Cyclopentenes; Angewandte Chemie International Edition; Vol. 53; No. 48; 13183-13187; PMCID PMC4433032; 10.1002/anie.201405854
• Choi, Junwon and Martín-Gago, Pablo, et el. (2014) Stereoconvergent Arylations and Alkenylations of Unactivated Alkyl Electrophiles: Catalytic Enantioselective Synthesis of Secondary Sulfonamides and Sulfones; Journal of the American Chemical Society; Vol. 136; No. 34; 12161-12165; PMCID PMC4151784; 10.1021/ja506885s
• Tan, Yichen and Muñoz-Molina, José María, et el. (2014) Oxygen nucleophiles as reaction partners in photoinduced, copper-catalyzed cross-couplings: O-arylations of phenols at room temperature; Chemical Science; Vol. 5; No. 7; 2831-2835; 10.1039/c4sc00368c
• Lee, Sarah Yunmi and Neufeind, Stefan, et el. (2014) Enantioselective Nucleophile-Catalyzed Synthesis of Tertiary Alkyl Fluorides via the α‑Fluorination of Ketenes: Synthetic and Mechanistic Studies; Journal of the American Chemical Society; PMCID PMC4091276; 10.1021/ja5044209
• Liang, Yufan and Fu, Gregory C. (2014) Catalytic Asymmetric Synthesis of Tertiary Alkyl Fluorides: Negishi Cross-Couplings of Racemic α,α-Dihaloketones; Journal of the American Chemical Society; Vol. 136; No. 14; 5520-5524; PMCID PMC4004247; 10.1021/ja501815p
• Cong, Huan and Fu, Gregory C. (2014) Catalytic Enantioselective Cyclization/Cross-Coupling with Alkyl Electrophiles; Journal of the American Chemical Society; Vol. 136; No. 10; 3788-3791; PMCID PMC3985453; 10.1021/ja500706v
• Do, Hien-Quang and Bachman, Shoshana, et el. (2014) Photoinduced, Copper-Catalyzed Alkylation of Amides with Unactivated Secondary Alkyl Halides at Room Temperature; Journal of the American Chemical Society; Vol. 136; No. 5; 2162-2167; 10.1021/ja4126609
• Do, Hien-Quang and Chandrashekar, E. R. R., et el. (2013) Nickel/Bis(oxazoline)-Catalyzed Asymmetric Negishi Arylations of Racemic Secondary Benzylic Electrophiles to Generate Enantioenriched 1,1-Diarylalkanes; Journal of the American Chemical Society; Vol. 135; No. 44; 16288-16291; PMCID PMC3869004; 10.1021/ja408561b
• Ziegler, Daniel T. and Choi, Junwon, et el. (2013) 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; Vol. 135; No. 35; 13107-13112; 10.1021/ja4060806
• Cordier, Christopher J. and Lundgren, Ryan J., et el. (2013) 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; Vol. 135; No. 30; 10946-10949; PMCID PMC3803154; 10.1021/ja4054114
• Uyeda, Christopher and Tan, Yichen, et el. (2013) A New Family of Nucleophiles for Photoinduced, Copper-Catalyzed Cross-Couplings via Single-Electron Transfer: Reactions of Thiols with Aryl Halides Under Mild Conditions (0 °C); Journal of the American Chemical Society; Vol. 135; No. 25; 9548-9552; 10.1021/ja404050f
• Bissember, Alex C. and Lundgren, Rylan J., et el. (2013) Transition-Metal-Catalyzed Alkylations of Amines with Alkyl Halides: Photoinduced, Copper-Catalyzed Couplings of Carbazoles; Angewandte Chemie International Edition; Vol. 52; No. 19; 5129-5133; 10.1002/anie.201301202
• Lundgren, Rylan J. and Wilsily, Ashraf, et el. (2013) Catalytic Asymmetric C-N Bond Formation: Phosphine-Catalyzed Intra- and Intermolecular γ-Addition of Nitrogen Nucleophiles to Allenoates and Alkynoates; Angewandte Chemie International Edition; Vol. 52; No. 9; 2525-2528; PMCID PMC3819219; 10.1002/anie.201208957
• Zultanski, Susan L. and Fu, Gregory C. (2013) Nickel-Catalyzed Carbon−Carbon Bond-Forming Reactions of Unactivated Tertiary Alkyl Halides: Suzuki Arylations; Journal of the American Chemical Society; Vol. 135; No. 2; 624-627; PMCID PMC3547142; 10.1021/ja311669p
• Creutz, Sidney E. and Lotito, Kenneth J., et el. (2012) Photoinduced Ullmann C–N Coupling: Demonstrating the Viability of a Radical Pathway; Science; Vol. 338; No. 6107; 647-651; 10.1126/science.1226458
• Binder, Jörg T. and Cordier, Christopher J., et el. (2012) 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; Vol. 134; No. 41; 17003-17006; PMCID PMC3474870; 10.1021/ja308460z
• Lee, Sarah Yunmi and Murphy, Jaclyn M., et el. (2012) Nonenzymatic Dynamic Kinetic Resolution of Secondary Alcohols via Enantioselective Acylation: Synthetic and Mechanistic Studies; Journal of the American Chemical Society; Vol. 134; No. 36; 15149-15153; PMCID PMC3447740; 10.1021/ja307425g
• Bissember, Alex C. and Levina, Anna, et el. (2012) A Mild, Palladium-Catalyzed Method for the Dehydrohalogenation of Alkyl Bromides: Synthetic and Mechanistic Studies; Journal of the American Chemical Society; Vol. 134; No. 34; 14232-14237; PMCID PMC3432975; 10.1021/ja306323x
• Dudnik, Alexander S. and Fu, Gregory C. (2012) Nickel-Catalyzed Coupling Reactions of Alkyl Electrophiles, Including Unactivated Tertiary Halides, To Generate Carbon–Boron Bonds; Journal of the American Chemical Society; Vol. 134; No. 25; 10693-10697; PMCID PMC3384763; 10.1021/ja304068t
• Choi, Junwon and Fu, Gregory C. (2012) Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent Negishi arylations and alkenylations of racemic α-bromonitriles; Journal of the American Chemical Society; Vol. 134; No. 22; 9102-9105; PMCID PMC3415582; 10.1021/ja303442q
• Wilsily, Ashraf and Tramutola, Francesco, et el. (2012) 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; Vol. 134; No. 13; 5794-5797; PMCID PMC3333791; 10.1021/ja301612y
• Zuhl, Andrea M. and Mohr, Justin T., et el. (2012) Competitive Activity-Based Protein Profiling Identifies Aza-β-Lactams as a Versatile Chemotype for Serine Hydrolase Inhibition; Journal of the American Chemical Society; Vol. 134; No. 11; 5068-5071; PMCID PMC3326416; 10.1021/ja300799t
• Oelke, Alexander J. and Sun, Jianwei, et el. (2012) Nickel-Catalyzed Enantioselective Cross-Couplings of Racemic Secondary Electrophiles That Bear an Oxygen Leaving Group; Journal of the American Chemical Society; Vol. 134; No. 6; 2966-2969; PMCID PMC3288265; 10.1021/ja300031w
• Fujiwara, Yuji and Sun, Jianwei, et el. (2011) Enantioselective carbon–sulfur bond formation: γ additions of aryl thiols to allenoates catalyzed by a chiral phosphepine; Chemical Science; Vol. 2; No. 11; 2196-2198; PMCID PMC3248350; 10.1039/c1sc00414j
• Zultanski, Susan L. and Fu, Gregory C. (2011) Catalytic Asymmetric γ-Alkylation of Carbonyl Compounds via Stereoconvergent Suzuki Cross-Couplings; Journal of the American Chemical Society; Vol. 133; No. 39; 15362-15364; PMCID PMC3183125; 10.1021/ja2079515
• Fujiwara, Yuji and Fu, Gregory C. (2011) 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; Vol. 133; No. 31; 12293-12297; PMCID PMC3150361; 10.1021/ja2049012
• Lu, Zhe and Wilsily, Ashraf, et el. (2011) Stereoconvergent Amine-Directed Alkyl–Alkyl Suzuki Reactions of Unactivated Secondary Alkyl Chlorides; Journal of the American Chemical Society; Vol. 133; No. 21; 8154-8157; PMCID PMC3102136; 10.1021/ja203560q
• Bachovchin, Daniel A. and Mohr, Justin T., et el. (2011) 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; Vol. 108; No. 17; 6811-6816; PMCID PMC3084096; 10.1073/pnas.1015248108
• Sinisi, Riccardo and Sun, Jianwei, et el. (2010) Phosphine-catalyzed asymmetric additions of malonate esters to γ-substituted allenoates and allenamides; Proceedings of the National Academy of Sciences of the United States of America; Vol. 107; No. 48; 20652-20654; PMCID PMC2996437; 10.1073/pnas.1003597107
• Lou, Sha and Fu, Gregory C. (2010) Palladium/Tris(tert-butyl)phosphine‐Catalyzed Suzuki Cross‐ Couplings in the Presence of Water; Advanced Synthesis and Catalysis; Vol. 352; No. 11‐12; 2081-2084; PMCID PMC3011868; 10.1002/adsc.201000267
• Lu, Zhe and Fu, Gregory C. (2010) Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides; Angewandte Chemie International Edition; Vol. 49; No. 37; 6676-6678; PMCID PMC3073318; 10.1002/anie.201003272
• Owston, Nathan A. and Fu, Gregory C. (2010) Asymmetric Alkyl−Alkyl Cross-Couplings of Unactivated Secondary Alkyl Electrophiles: Stereoconvergent Suzuki Reactions of Racemic Acylated Halohydrins; Journal of the American Chemical Society; Vol. 132; No. 34; 11908-11909; PMCID PMC2929007; 10.1021/ja105924f
• Lundin, Pamela M. and Fu, Gregory C. (2010) Asymmetric Suzuki Cross-Couplings of Activated Secondary Alkyl Electrophiles: Arylations of Racemic α-Chloroamides; Journal of the American Chemical Society; Vol. 132; No. 32; 11027-11029; PMCID PMC2924160; 10.1021/ja105148g
• Lou, Sha and Fu, Gregory C. (2010) Enantioselective Alkenylation via Nickel-Catalyzed Cross-Coupling with Organozirconium Reagents; Journal of the American Chemical Society; Vol. 132; No. 14; 5010-5011; PMCID PMC2860276; 10.1021/ja1017046
• Sun, Jianwei and Fu, Gregory C. (2010) Phosphine-Catalyzed Formation of Carbon−Sulfur Bonds: Catalytic Asymmetric Synthesis of γ-Thioesters; Journal of the American Chemical Society; Vol. 132; No. 13; 4568-4569; PMCID PMC2850260; 10.1021/ja101251d
• Lou, Sha and Fu, Gregory C. (2010) Nickel/Bis(oxazoline)-Catalyzed Asymmetric Kumada Reactions of Alkyl Electrophiles: Cross-Couplings of Racemic α-Bromoketones; Journal of the American Chemical Society; Vol. 132; No. 4; 1264-1266; PMCID PMC2814537; 10.1021/ja909689t
• Wilson, Jonathan E. and Sun, Jianwei, et el. (2010) Stereoselective Phosphine-Catalyzed Synthesis of Highly Functionalized Diquinanes; Angewandte Chemie International Edition; Vol. 49; No. 1; 161-163; 10.1002/anie.200905125
• Lou, Sha and Fu, Gregory C. (2010) Palladium-catalyzed alkyl-alkyl Suzuki cross-coupling of primary alkyl bromides at room temperature: (13-cholorotridecyloxy)triethylsilane; Organic Syntheses; Vol. 87; 299-309; PMCID PMC3008580; 10.15227/orgsyn.087.0299
• Lou, Sha and Fu, Gregory C. (2010) 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; Vol. 87; 330-338; PMCID PMC3083032; 10.15227/orgsyn.087.0330
• Lou, Sha and Fu, Gregory C. (2010) 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; Organic Syntheses; Vol. 87; 310-316; PMCID PMC3100209; 10.15227/orgsyn.087.0310
• Lou, Sha and Fu, Gregory C. (2010) 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; Vol. 87; 317-329; PMCID PMC3100190; 10.15227/orgsyn.087.0317
• Smith, Sean W. and Fu, Gregory C. (2009) Asymmetric Carbon−Carbon Bond Formation γ to a Carbonyl Group: Phosphine-Catalyzed Addition of Nitromethane to Allenes; Journal of the American Chemical Society; Vol. 131; No. 40; 14231-14233; PMCID PMC2758928; 10.1021/ja9061823
• Dochnahl, Maximilian and Fu, Gregory C. (2009) Catalytic Asymmetric Cycloaddition of Ketenes and Nitroso Compounds: Enantioselective Synthesis of α-Hydroxycarboxylic Acid Derivatives; Angewandte Chemie International Edition; Vol. 48; No. 13; 2391-2393; PMCID PMC2728616; 10.1002/anie.200805805
• Chung, Ying Kit and Fu, Gregory C. (2009) Phosphine-Catalyzed Enantioselective Synthesis of Oxygen Heterocycles; Angewandte Chemie International Edition; Vol. 48; No. 12; 2225-2227; PMCID PMC2747790; 10.1002/anie.200805377
• Lundin, Pamela M. and Esquivias, Jorge, et el. (2008) Catalytic Asymmetric Cross-Couplings of Racemic α-Bromoketones with Arylzinc Reagents; Angewandte Chemie International Edition; Vol. 48; No. 1; 154-156; PMCID PMC2790061; 10.1002/anie.200804888
• Fu, Gregory C. (2008) 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; Vol. 41; No. 11; 1555-1564; PMCID PMC2645957; 10.1021/ar800148f
• Grubbs, Robert H. and Miller, Scott J., et el. (1995) Ring-Closing Metathesis and Related Processes in Organic Synthesis; Accounts of Chemical Research; Vol. 28; No. 11; 446-452; 10.1021/ar00059a002
• Fujimura, Osamu and Fu, Gregory C., et el. (1994) The Synthesis of Cyclic Enol Ethers via Molybdenum Alkylidene-Catalyzed Ring-Closing Metathesis; Journal of Organic Chemistry; Vol. 59; No. 15; 4029-4031; 10.1021/jo00094a002
• Fu, Gregory C. and Grubbs, Robert H. (1993) Synthesis of cycloalkenes via alkylidene-mediated olefin metathesis and carbonyl olefination; Journal of the American Chemical Society; Vol. 115; No. 9; 3800-3801; 10.1021/ja00062a066
• Fu, Gregory C. and Grubbs, Robert H. (1992) The application of catalytic ring-closing olefin metathesis to the synthesis of unsaturated oxygen heterocycles; Journal of the American Chemical Society; Vol. 114; No. 13; 5426-5427; 10.1021/ja00039a065