Direct enantioselective α-amination of amides guided by DFT prediction of E/Z selectivity in a sulfonium intermediate
暂无分享,去创建一个
[1] M. Feng,et al. Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes , 2022, Angewandte Chemie.
[2] M. Feng,et al. Challenges and Breakthroughs in Selective Amide Activation , 2022, Angewandte Chemie.
[3] M. Feng,et al. Deployment of Sulfinimines in Charge-Accelerated Sulfonium Rearrangement Enables a Surrogate Asymmetric Mannich Reaction , 2022, Journal of the American Chemical Society.
[4] Qi‐Lin Zhou,et al. Enantioselective synthesis of amino acids from ammonia , 2022, Nature Catalysis.
[5] E. Meggers,et al. Stereocontrolled 1,3-nitrogen migration to access chiral α-amino acids , 2022, Nature Chemistry.
[6] C. Nevado,et al. Asymmetric, visible light-mediated radical sulfinyl-Smiles rearrangement to access all-carbon quaternary stereocentres , 2021, Nature Chemistry.
[7] Ian D. Williams,et al. Chiral Phosphoric Acid Catalyzed Enantioselective Synthesis of α-Tertiary Amino Ketones from Sulfonium Ylides. , 2020, Journal of the American Chemical Society.
[8] A. Fontana,et al. Hydrogen Bonding Phase-Transfer Catalysis with Ionic Reactants: Enantioselective Synthesis of γ-Fluoroamines , 2020, Journal of the American Chemical Society.
[9] E. Corey,et al. A Method for the Catalytic Enantioselective Synthesis of Chiral α-Azido and α-Amino Ketones from Racemic α-Bromo Ketones, and Its Generalization to the Formation of Bonds to C, O, and S. , 2019, Journal of the American Chemical Society.
[10] L. González,et al. Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles , 2019, Journal of the American Chemical Society.
[11] N. Maulide,et al. A Chemoselective α-Oxytriflation Enables the Direct Asymmetric Arylation of Amides , 2019, Chem.
[12] N. Maulide,et al. Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts , 2019, Chemical reviews.
[13] H. Sitte,et al. α-Fluorination of carbonyls with nucleophilic fluorine , 2019, Nature Chemistry.
[14] N. Maulide,et al. Amide activation: an emerging tool for chemoselective synthesis. , 2018, Chemical Society reviews.
[15] D. Kaldre,et al. Stereodivergent synthesis of 1,4-dicarbonyls by traceless charge–accelerated sulfonium rearrangement , 2018, Science.
[16] Jian-Liang Ye,et al. Versatile One-Pot Synthesis of Polysubstituted Cyclopent-2-enimines from α,β-Unsaturated Amides: Imino-Nazarov Reaction. , 2018, Angewandte Chemie.
[17] G. Evano,et al. Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis , 2017, Synthesis.
[18] M. Blaskovich. Unusual Amino Acids in Medicinal Chemistry. , 2016, Journal of medicinal chemistry.
[19] Stefan A. Ruider,et al. Chemo- and Stereoselective Transition-Metal-Free Amination of Amides with Azides , 2016, Journal of the American Chemical Society.
[20] A. Van der Aa,et al. Safety, pharmacokinetics and pharmacodynamics of GLPG0974, a potent and selective FFA2 antagonist, in healthy male subjects , 2016, British journal of clinical pharmacology.
[21] G. C. Fu,et al. Asymmetric copper-catalyzed C-N cross-couplings induced by visible light , 2016, Science.
[22] T. Jacobs,et al. Employing Unnatural Amino Acids in the Preparation of Biooconjugates , 2016, Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry.
[23] F. Salituro,et al. Discovery of VX-509 (Decernotinib): A Potent and Selective Janus Kinase 3 Inhibitor for the Treatment of Autoimmune Diseases. , 2015, Journal of medicinal chemistry.
[24] F. Toste,et al. Direct asymmetric amination of α-branched cyclic ketones catalyzed by a chiral phosphoric acid. , 2015, Journal of the American Chemical Society.
[25] B. Vergani,et al. Amino acidic scaffolds bearing unnatural side chains: an old idea generates new and versatile tools for the life sciences. , 2014, Bioorganic & medicinal chemistry letters.
[26] C. Farés,et al. Chemoselective intermolecular α-arylation of amides. , 2014, Angewandte Chemie.
[27] Bin Xu,et al. Enantioselective N-H insertion reaction of α-aryl α-diazoketones: an efficient route to chiral α-aminoketones. , 2014, Angewandte Chemie.
[28] M. Terada,et al. Development of a chiral bis(guanidino)iminophosphorane as an uncharged organosuperbase for the enantioselective amination of ketones. , 2013, Journal of the American Chemical Society.
[29] Lili Lin,et al. New electrophilic addition of α-diazoesters with ketones for enantioselective C-N bond formation. , 2011, Journal of the American Chemical Society.
[30] K. K. Hii,et al. Transition metal catalyzed enantioselective α-heterofunctionalization of carbonyl compounds. , 2011, Chemical reviews.
[31] Peter G Schultz,et al. Adding new chemistries to the genetic code. , 2010, Annual review of biochemistry.
[32] J. Ellman,et al. Synthesis and applications of tert-butanesulfinamide. , 2010, Chemical reviews.
[33] Pei‐Qiang Huang,et al. Direct, one-pot sequential reductive alkylation of lactams/amides with Grignard and organolithium reagents through lactam/amide activation. , 2010, Angewandte Chemie.
[34] P. Schultz,et al. Beyond the Canonical 20 Amino Acids: Expanding the Genetic Lexicon* , 2010, The Journal of Biological Chemistry.
[35] J. Sansano,et al. Catalytic Asymmetric Synthesis of α-Amino Acids , 2007 .
[36] Elaine C. Lee,et al. Copper-Catalyzed Asymmetric N−H Insertion Reactions: Couplings of Diazo Compounds with Carbamates to Generate α-Amino Acids , 2007 .
[37] M. D. Hill,et al. Single-step synthesis of pyrimidine derivatives. , 2006, Journal of the American Chemical Society.
[38] J. Deschamps,et al. 1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors. , 2006, Journal of medicinal chemistry.
[39] Hisashi Yamamoto,et al. Enantioselective O- and N-nitroso aldol synthesis of tin enolates. Isolation of three BINAP-silver complexes and their role in regio- and enantioselectivity. , 2004, Journal of the American Chemical Society.
[40] Jun‐An Ma. Recent Developments in the Catalytic Asymmetric Synthesis of α‐ and β‐Amino Acids , 2003 .
[41] B. List. Direct catalytic asymmetric alpha-amination of aldehydes. , 2002, Journal of the American Chemical Society.
[42] M. Grenon,et al. Spectroscopic studies of the electrophilic activation of amides with triflic anhydride and pyridine , 2001 .
[43] H. Rapoport,et al. Enantiospecific Synthesis of Heterocycles from α-Amino Acids , 1996 .
[44] D. Ager,et al. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis. , 1996, Chemical reviews.
[45] L. Ghosez,et al. A Convenient Procedure for the Synthesis of Cyclobutanones , 1974 .
[46] L. González,et al. An Asymmetric Redox Arylation: Chirality Transfer from Sulfur to Carbon through a Sulfonium [3,3]-Sigmatropic Rearrangement. , 2017, Angewandte Chemie.
[47] M. Khrestchatisky,et al. Synthetic therapeutic peptides: science and market. , 2010, Drug discovery today.