FeCl3-catalyzed three-component aryl-selenylation of alkenes
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[1] D. Back,et al. Diorganyl Diselenides and Iron(III) Chloride Drive the Regio- and Stereoselectivity in the Selenation of Ynamides. , 2020, The Journal of organic chemistry.
[2] Daniel K. W. Wang,et al. Transition metal-free coupling reactions of benzylic trimethylammonium salts with di(hetero)aryl disulfides and diselenides. , 2020, Chemical communications.
[3] C. Yang,et al. Three-component aminoselenation of alkenes via visible-light enabled Fe-catalysis , 2020 .
[4] P. Evans,et al. A Simple Zinc-Mediated Method for Selenium Addition to Michael Acceptors , 2020, Molecules.
[5] Qingle Zeng,et al. A recyclable Amberlyst-15-catalyzed three-component reaction in water to synthesize diarylmethyl sulfones , 2019, Green Chemistry.
[6] Ze Tan,et al. Silver-Promoted Decarboxylative Sulfonylation of Aromatic Carboxylic Acids with Sodium Sulfinates. , 2019, The Journal of organic chemistry.
[7] Xuefeng Jiang,et al. Recent progress in selenium-catalyzed organic reactions , 2019, Organic Chemistry Frontiers.
[8] P. Anbarasan,et al. Trifluoromethylthiolative 1,2-difunctionalization of alkenes with diselenides and AgSCF3. , 2019, Chemical communications.
[9] T. Wirth,et al. Selenium reagents as catalysts , 2019, Catalysis Science & Technology.
[10] Li‐Zhu Wu,et al. Preparation of Heterocycles via Visible-Light-Driven Aerobic Selenation of Olefins with Diselenides. , 2019, Organic letters.
[11] Wenlong Jiang,et al. Copper-Catalyzed Stereospecific C–S Coupling Reaction of Enantioenriched Tertiary Benzylic Amines via in Situ Activation with Methyl Triflate , 2018, ACS Catalysis.
[12] E. Lenardão,et al. Selenomethoxylation of Alkenes Promoted by Oxone , 2018 .
[13] M. Iwaoka,et al. Protein Folding in the Presence of Water‐Soluble Cyclic Diselenides with Novel Oxidoreductase and Isomerase Activities , 2018, Chembiochem : a European journal of chemical biology.
[14] Yiming Li,et al. Visible light-promoted, iodine-catalyzed selenoalkoxylation of olefins with diselenides and alcohols in the presence of hydrogen peroxide/air oxidant: an efficient access to α-alkoxyl selenides , 2018, Science China Chemistry.
[15] Li‐Zhu Wu,et al. Visible-light-mediated aerobic selenation of (hetero)arenes with diselenides , 2017 .
[16] Naixing Wang,et al. Recent Advances in Radical Difunctionalization of Simple Alkenes , 2017 .
[17] S. Ortgies,et al. Oxidative Alkene Functionalizations via Selenium-π-Acid Catalysis , 2017 .
[18] K. Sun,et al. Direct access to β-seleno sulfones at room temperature through selenosulfonylation of alkenes , 2017, Science China Chemistry.
[19] E. Tang,et al. Catalytic Selenium-Promoted Intermolecular Friedel-Crafts Alkylation with Simple Alkenes. , 2016, Organic letters.
[20] T. Wirth. Kleine Organoselenverbindungen: mehr als nur Mimetika der Glutathion‐Peroxidase , 2015 .
[21] R. Peddinti,et al. Iodine catalyzed cross-dehydrogenative C–S coupling by C(sp2)–H bond activation: direct access to aryl sulfides from aryl thiols , 2015 .
[22] F. Nedel,et al. New organochalcogen multitarget drug: synthesis and antioxidant and antitumoral activities of chalcogenozidovudine derivatives. , 2015, Journal of medicinal chemistry.
[23] A. A. Vieira,et al. Catalytic chalcogenylation under greener conditions: a solvent-free sulfur- and seleno-functionalization of olefins via I2/DMSO oxidant system. , 2015, The Journal of organic chemistry.
[24] L. Sancineto,et al. “The green side of the moon: ecofriendly aspects of organoselenium chemistry” , 2014 .
[25] C. Nevado,et al. Addition of CF3 across unsaturated moieties: a powerful functionalization tool , 2014, Chemical Society reviews.
[26] S. Chemler,et al. Catalytic Aminohalogenation of Alkenes and Alkynes. , 2013, ACS catalysis.
[27] Claudio Martínez,et al. Development of intramolecular vicinal diamination of alkenes: from palladium to bromine catalysis. , 2013, The Journal of organic chemistry.
[28] D. Back,et al. Bis-vinyl selenides obtained via iron(III) catalyzed addition of PhSeSePh to alkynes: synthesis and antinociceptive activity. , 2013, Organic & biomolecular chemistry.
[29] T. Wirth,et al. Selenenylations of alkenes with styrene nucleophiles , 2012 .
[30] M. Detty,et al. Imidazolium-containing diselenides for catalytic oxidations with hydrogen peroxide and sodium bromide in aqueous solutions , 2012 .
[31] B. Kim,et al. p38 mitogen-activated protein kinase is a key regulator of 5-phenylselenyl- and 5-methylselenyl-methyl-2'-deoxyuridine-induced apoptosis in human HL-60 cells. , 2012, Biochemical and biophysical research communications.
[32] R. Guo,et al. Iron salt, a cheap, highly efficient and environment-friendly metal catalyst for Se–Se bond cleavage and the further reaction with methylenecyclopropanes under mild conditions , 2011 .
[33] S. Stahl,et al. Palladium(II)-catalyzed alkene functionalization via nucleopalladation: stereochemical pathways and enantioselective catalytic applications. , 2011, Chemical reviews.
[34] S. Bhattacharya,et al. Synthesis and biological evaluation of novel spiro 6-methoxytetralin-1,3'-pyrrolidine based organoselenocyanates against cadmium-induced oxidative and hepatic damage in mice. , 2010, European journal of medicinal chemistry.
[35] Devender Singh,et al. An efficient one-pot synthesis of symmetrical diselenides or ditellurides from halides with CuO nanopowder/Se0 or Te0/base. , 2010, Organic letters.
[36] R. B. Sunoj,et al. Organoselenium chemistry: role of intramolecular interactions. , 2010, Chemical reviews.
[37] C. Bolm. A new iron age. , 2009, Nature chemistry.
[38] A. Ogawa,et al. Copper(0)-induced deselenative insertion of N,N-disubstituted selenoamides into acetylenic C-H bond leading to propargylamines. , 2009, Organic letters.
[39] W. J. Choi,et al. Design and synthesis of novel 2',3'-dideoxy-4'-selenonucleosides as potential antiviral agents. , 2008, Bioorganic & medicinal chemistry.
[40] Shusheng Zhang,et al. Determination of physiological thiols by electrochemical detection with piazselenole and its application in rat breast cancer cells 4T-1. , 2008, Journal of the American Chemical Society.
[41] Ping Wu,et al. Novel Brønsted acid catalyzed three-component alkylations of indoles with N-phenylselenophthalimide and styrenes. , 2007, Organic letters.
[42] A. Misra,et al. Synthesis of thio- and selenoglycosides by cleavage of dichalconides in the presence of zinc/zinc chloride and reaction with glycosyl bromides☆ , 2006 .
[43] Ken Tanaka,et al. Rhodium-catalyzed reductive coupling of disulfides and diselenides with alkyl halides, using hydrogen as a reducing agent. , 2005, Organic letters.
[44] Y. Nishibayashi,et al. Asymmetric carboselenenylation reaction of alkenes with aromatic compounds. , 2005, Angewandte Chemie.
[45] Y. Nishibayashi,et al. Stereospecific carbon–carbon bond formation by the reaction of a chiral episelenonium ion with aromatic compounds , 2004 .
[46] G. Zeni,et al. Stereoselective synthesis of enynes by nickel-catalyzed cross-coupling of divinylic chalcogenides with alkynes. , 2003, The Journal of organic chemistry.
[47] Jeffrey D. Neighbors,et al. A cascade cyclization approach to schweinfurthin B. , 2002, Organic letters.
[48] A. Singh. Organotellurium ligands — designing and complexation reactions , 2002 .
[49] S. Knapp,et al. Synthesis of the sialidase inhibitor siastatin B. , 2000, Organic letters.
[50] J. H. Rigby,et al. Studies on the narciclasine alkaloids: Total synthesis of (+)- narciclasine and (+)-pancratistatin , 2000 .
[51] W. D. Mont. Book Review: Organoselenium Chemistry. Edited by D. Liotta , 1988 .
[52] H. Reich,et al. ORGANOSELENIUM CHEMISTRY, ALPHA-LITHIO SELENOXIDES AND SELENIDES, PREPARATION AND FURTHER TRANSFORMATION TO OLEFINS, DIENES, AND ALLYLIC ALCOHOLS , 1975 .