Fu, Gregory

Combined 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 Chung-Wei (2019) Nucleophilic substitution reactions: A radical alternative to SN_1 and SN_2 reactions
• 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
• Fu, Gregory C. (2018) Award Address (Herbert C. Brown Award for Creative Research in Synthetic Methods sponsored by the Purdue Borane Research Fund and the Herbert C. Brown Award Endowment). Nucleophilic substitution reactions: A radical alternative to S_N1 and S_N2 reactions
• 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
• Schwarzwalder, Gregg and Fu, Gregory (2017) Catalytic asymmetric synthesis of alkylsilanes enabled by stereoconvergent nickel-catalyzed cross-coupling
• 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
• Fu, Gregory C. (2017) Metal-catalyzed cross-coupling reactions of alkyl electrophiles
• 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
• Fu, Gregory C. (2016) Metal-catalyzed cross-coupling reactions of alkyl electrophiles
• 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
• Ahn, Jun Myun and Hannoun, Kareem, et el. (2015) Mechanistic insights into photo-induced, copper-catalyzed alkylations of amines
• 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) Metal-catalyzed cross-coupling reactions of alkyl electrophiles
• 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
• Peters, Jonas C. and Fu, Gregory (2014) Catalytic cross-coupling with copper and light
• 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 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
• 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 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
• 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
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