Synthesis of N-sulfenyl-sulfoximines and -sulfenamides through a metal-free N–H/S–H dehydrocoupling reaction
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Qingle Zeng | Jie Feng | Lu Yang | Mei Qiao
[1] Guanyu Yang,et al. Reusable cobalt-phthalocyanine in water: efficient catalytic aerobic oxidative coupling of thiols to construct S–N/S–S bonds , 2017 .
[2] A. Gupta,et al. Iodine-Catalyzed C-N Bond Formation: Synthesis of 3-Aminoquinoxalinones under Ambient Conditions. , 2017, The Journal of organic chemistry.
[3] C. Bolm,et al. 1,2-Benzothiazines from Sulfoximines and Allyl Methyl Carbonate by Rhodium-Catalyzed Cross-Coupling and Oxidative Cyclization. , 2017, Organic letters.
[4] C. Bolm,et al. Sulfoximines from a Medicinal Chemist's Perspective: Physicochemical and in vitro Parameters Relevant for Drug Discovery. , 2017, European journal of medicinal chemistry.
[5] Qingle Zeng,et al. A New Type of Chiral Cyclic Sulfinamide–Olefin Ligands for Rhodium‐Catalyzed Asymmetric Addition , 2016 .
[6] Jin‐Tao Yu,et al. Copper-catalyzed N-thioetherification of sulfoximines using disulfides. , 2016, Chemical communications.
[7] Qingle Zeng,et al. Catalyst-free Synthesis of 2-(tert-Butyldisulfanyl) Heterocycles from tert-Butanesulfinamide and Mercapto-substituted Imidazoles, Tetrazole, Pyrimidine and Pyridine , 2016 .
[8] K. R. Prabhu,et al. Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: A Regioselective Sulfenylation of Imidazoheterocycles Using Dimethyl Sulfoxide as an Oxidant. , 2016, The Journal of organic chemistry.
[9] G. Sekar,et al. Palladium Nanoparticles Catalyzed Aroylation of NH‐Sulfoximines with Aryl Iodides. , 2016 .
[10] Phil Ho Lee,et al. Synthesis of 1,2-Benzothiazines by a Rhodium-Catalyzed Domino C-H Activation/Cyclization/Elimination Process from S-Aryl Sulfoximines and Pyridotriazoles. , 2016, Organic letters.
[11] Saima,et al. Cooperative catalysis by bovine serum albumin-iodine towards cascade oxidative coupling-C(sp(2))-H sulfenylation of indoles/hydroxyaryls with thiophenols on water. , 2016, Organic & biomolecular chemistry.
[12] C. Pan,et al. Radical N-arylation/alkylation of sulfoximines , 2016 .
[13] Xinquan Hu,et al. Metal-free, iodine-catalyzed regioselective sulfenylation of indoles with thiols , 2016 .
[14] N. Taniguchi. Copper‐Catalyzed Oxidative Synthesis of Sulfinamides Using Thiols or Disulfides with Amines , 2016 .
[15] R. Peddinti,et al. Metal-free synthesis of sulfonamides via iodine-catalyzed oxidative coupling of sulfonyl hydrazides and amines , 2016 .
[16] Jin‐Tao Yu,et al. The N-silylation of sulfoximines. , 2015, Organic & biomolecular chemistry.
[17] T. Conrads,et al. The orally active and bioavailable ATR kinase inhibitor AZD6738 potentiates the anti-tumor effects of cisplatin to resolve ATM-deficient non-small cell lung cancer in vivo , 2015, Oncotarget.
[18] Jin‐Tao Yu,et al. Copper-catalyzed N-methylation/ethylation of sulfoximines. , 2015, Organic & biomolecular chemistry.
[19] Wanrong Dong,et al. Transition metal-free aroylation of NH-sulfoximines with methyl arenes. , 2015, Chemical communications.
[20] Yu Na Lim,et al. Copper-Catalyzed Synthesis of N-Formyl/Acylsulfenamides and -thiosulfonamides , 2015 .
[21] Dominique M. Roberge,et al. Development of a Continuous Flow Sulfoxide Imidation Protocol Using Azide Sources under Superacidic Conditions , 2015 .
[22] M. Jeganmohan,et al. Ruthenium- and palladium-catalyzed consecutive coupling and cyclization of aromatic sulfoximines with phenylboronic acids: an efficient route to dibenzothiazines. , 2015, Chemical communications.
[23] Hua Wang,et al. Metal-Free Iodine-Catalyzed Direct Arylthiation of Substituted Anilines with Thiols. , 2015, The Journal of organic chemistry.
[24] C. Bolm,et al. N-Trifluoromethylthiolated Sulfoximines. , 2015, Organic letters.
[25] C. Bolm,et al. Sulfur imidations: access to sulfimides and sulfoximines. , 2015, Chemical Society reviews.
[26] S. Pan,et al. nBu4NI‐Catalyzed α‐Benzoxylation of Ketones with Terminal Aryl Alkenes , 2015 .
[27] Yan Jiang,et al. Copper-catalyzed oxidative C(sp(3))-H/N-H coupling of sulfoximines and amides with simple alkanes via a radical process. , 2015, Chemical communications.
[28] Jeh-Jeng Wang,et al. I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles. , 2015, Organic letters.
[29] Hye‐Young Jang,et al. Copper-catalyzed oxidative N-S bond formation for the synthesis of N-sulfenylimines. , 2015, Organic letters.
[30] S. Berteina‐Raboin,et al. Iodine-catalyzed regioselective sulfenylation of imidazoheterocycles in PEG400 , 2015 .
[31] Hui Yu,et al. Dehydrogenative cyclization of N-acyl dipeptide esters for the synthesis of imidazolidin-4-ones , 2015 .
[32] Qingle Zeng,et al. An environment-friendly synthesis of 4(3H)-quinazolinones , 2015 .
[33] C. Supuran,et al. A Class of 4-Sulfamoylphenyl-ω-aminoalkyl Ethers with Effective Carbonic Anhydrase Inhibitory Action and Antiglaucoma Effects , 2014, Journal of medicinal chemistry.
[34] D. Zhang-Negrerie,et al. Direct oxidative coupling of enamines and electron-deficient amines: TBAI/TBHP-mediated synthesis of substituted diaminoalkenes under metal-free conditions. , 2014, Organic letters.
[35] M. Sukwattanasinitt,et al. Hypervalent Iodine(III)‐Promoted Metal‐Free S–H Activation: An Approach for the Construction of S–S, S–N, and S–C Bonds , 2014 .
[36] Ximing Xu,et al. Synthesis and biological activities of novel pleuromutilin derivatives with a substituted thiadiazole moiety as potent drug-resistant bacteria inhibitors. , 2014, Journal of medicinal chemistry.
[37] Hui Yu,et al. Peroxidation of C-H bonds adjacent to an amide nitrogen atom under mild conditions. , 2014, Organic letters.
[38] C. Bolm,et al. N-Alkylations of NH-Sulfoximines and NH-Sulfondiimines with Alkyl Halides Mediated by Potassium Hydroxide in Dimethyl Sulfoxide , 2014 .
[39] C. Bolm,et al. N-Arylations of sulfoximines with 2-arylpyridines by copper-mediated dual N-H/C-H activation. , 2014, Organic letters.
[40] J. T. Njardarson,et al. Data-mining for sulfur and fluorine: an evaluation of pharmaceuticals to reveal opportunities for drug design and discovery. , 2014, Journal of medicinal chemistry.
[41] Yuanjiang Pan,et al. Copper-mediated S-N formation via an oxygen-activated radical process: a new synthesis method for sulfonamides. , 2014, Chemical communications.
[42] R. Kunz,et al. Small molecule disruptors of the glucokinase-glucokinase regulatory protein interaction: 3. Structure-activity relationships within the aryl carbinol region of the N-arylsulfonamido-N'-arylpiperazine series. , 2014, Journal of medicinal chemistry.
[43] Hui Yu,et al. TBHP/TBAI-Promoted Oxidative Cyclization of o-Acylphenols for the Construction of 2-Aryloxybenzofuran-3(2H)-ones , 2014, Synlett.
[44] X. Wan,et al. Iodide-catalyzed synthesis of N-nitrosamines via C-N cleavage of nitromethane. , 2013, The Journal of organic chemistry.
[45] C. Bolm,et al. Rhodium-catalyzed oxidative annulation of sulfoximines and alkynes as an approach to 1,2-benzothiazines. , 2013, Angewandte Chemie.
[46] U. Lücking. Sulfoximines: a neglected opportunity in medicinal chemistry. , 2013, Angewandte Chemie.
[47] M. Petrov,et al. A new synthesis of benzo[b]thiophene-2-thiolates and their derivatives via base-promoted transformation of 4-(2-mercaptophenyl)-1,2,3-thiadiazoles. , 2013, Organic letters.
[48] M. Kanai,et al. Copper-catalyzed intramolecular N-S bond formation by oxidative dehydrogenative cyclization. , 2013, The Journal of organic chemistry.
[49] Julia M. Schulze,et al. The Lab Oddity Prevails: Discovery of Pan‐CDK Inhibitor (R)‐S‐Cyclopropyl‐S‐(4‐{[4‐{[(1R,2R)‐2‐hydroxy‐1‐methylpropyl]oxy}‐5‐(trifluoromethyl)pyrimidin‐2‐yl]amino}phenyl)sulfoximide (BAY 1000394) for the Treatment of Cancer , 2013, ChemMedChem.
[50] C. Bolm,et al. Copper-catalyzed oxidative cross-coupling of sulfoximines and alkynes. , 2013, Angewandte Chemie.
[51] B. Nachtsheim,et al. Iodide-catalyzed halocyclization/cycloaddition/elimination cascade reaction. , 2013, The Journal of organic chemistry.
[52] T. Miura,et al. Molecular iodine catalyzed cross-dehydrogenative coupling reaction between two sp3 C-H bonds using hydrogen peroxide. , 2013, Organic letters.
[53] D. Ginger,et al. A one pot organic/CdSe nanoparticle hybrid material synthesis with in situ π-conjugated ligand functionalization. , 2013, Chemical communications.
[54] Zhiyong Wang,et al. Selective iodine-catalyzed intermolecular oxidative amination of C(sp3)-H bonds with ortho-carbonyl-substituted anilines to give quinazolines. , 2012, Angewandte Chemie.
[55] P. Lienau,et al. BAY 1000394, a Novel Cyclin-Dependent Kinase Inhibitor, with Potent Antitumor Activity in Mono- and in Combination Treatment upon Oral Application , 2012, Molecular Cancer Therapeutics.
[56] Qingle Zeng,et al. Synthesis of phenothiazines via ligand-free CuI-catalyzed cascade C-S and C-N coupling of aryl ortho-dihalides and ortho-aminobenzenethiols. , 2012, Chemical communications.
[57] R. Varma,et al. Copper‐Catalyzed Ultrasound‐Expedited N‐Arylation of Sulfoximines using Diaryliodonium Salts , 2012 .
[58] C. Xi,et al. Concise approach to benzisothiazol-3(2H)-one via copper-catalyzed tandem reaction of o-bromobenzamide and potassium thiocyanate in water. , 2012, The Journal of organic chemistry.
[59] Amit Kumar,et al. An efficient copper mediated synthetic methodology for benzo[d]isothiazol-3(2H)-ones and related sulfur–nitrogen heterocycles , 2012 .
[60] C. Bolm,et al. Copper-catalyzed direct sulfoximination of azoles and polyfluoroarenes under ambient conditions. , 2011, Organic letters.
[61] A. Edmunds,et al. Synthesis of CF3-substituted sulfoximines from sulfonimidoyl fluorides. , 2011, Organic letters.
[62] N. Taniguchi. Copper‐Catalyzed Formation of Sulfur–Nitrogen Bonds by Dehydrocoupling of Thiols with Amines , 2010 .
[63] S. Waldvogel,et al. Oxidative coupling of diaryldisulfides by MoCl5 to thianthrenes. , 2009, Chemistry.
[64] N. Taniguchi. Copper-Catalyzed Synthesis of Sulfenamides Utilizing Diaryl Disulfides with Alkyl Amines , 2007 .
[65] H. Gais. Development of New Methods for Asymmetric Synthesis Based on Sulfoximines , 2007 .
[66] Tina Talreja,et al. Design and synthesis of classical and nonclassical 6-arylthio-2,4-diamino-5-ethylpyrrolo[2,3-d]pyrimidines as antifolates. , 2007, Journal of medicinal chemistry.
[67] V. Nair,et al. An efficient synthesis of isothiazolidines via sulfonium ylides formed by the reaction of thietanes and nitrene , 2006 .
[68] Yufen Zhao,et al. Vanadium-Catalyzed Enantioselective Sulfoxidation and Concomitant, Highly Efficient Kinetic Resolution Provide High Enantioselectivity and Acceptable Yields of Sulfoxides , 2005 .
[69] Robin D. Rogers,et al. Polyethylene glycol and solutions of polyethylene glycol as green reaction media , 2005 .
[70] Xuechuan Hong,et al. New synthesis of benzothiazines and benzoisothiazoles containing a sulfoximine functional group. , 2005, Organic letters.
[71] C. Bolm,et al. Sulfoximines: Synthesis and Catalytic Applications , 2004 .
[72] F. Gantner,et al. An Orally Bioavailable Small Molecule Antagonist of CRTH2, Ramatroban (BAY u3405), Inhibits Prostaglandin D2-Induced Eosinophil Migration in Vitro , 2003, Journal of Pharmacology and Experimental Therapeutics.
[73] T. Nabeshima,et al. Synthesis of redox active large macrocyclic hosts and the recognition of secondary ammonium salts , 2003 .
[74] W. Greenlee,et al. Design and synthesis of ether analogues as potent and selective M2 muscarinic receptor antagonists. , 2001, Bioorganic & medicinal chemistry letters.
[75] M. Reggelin,et al. Sulfoximines: Structures, Properties and Synthetic Applications , 2000 .
[76] S. Ōae,et al. Preparation of S,S-diphenylsulfilimines, -sulfoximines, and -N-(p-tolylsulfonyl)sulfonediimines N-substituted with sulfur groups of different oxidation states , 1984 .
[77] T. Moran,et al. Toxic Factor from ‘Agenized’ Proteins: Methionine as the Essential Reactant , 1950, Nature.
[78] A. Marble. Glibenclamide, a New Sulphonylurea: Whither Oral Hypoglycaemic Agents? , 2012, Drugs.
[79] C. B. Burns,et al. Comparison of Zafirlukast (Accolate®) Absorption After Oral and Colonic Administration in Humans , 2004, Pharmaceutical Research.