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) 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) 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
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
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