Silver-catalyzed Vinylic C–F Bond Activation: Synthesis of 2-Fluoroindoles from β,β-Difluoro-o-sulfonamidostyrenes
暂无分享,去创建一个
[1] S. Cao,et al. Synthesis of Exocyclic Trisubstituted Alkenes via Nickel‐ Catalyzed Kumada‐Type Cross‐Coupling Reaction of gem‐ Difluoroalkenes with Di‐Grignard Reagents , 2016 .
[2] T. Ichitsuka,et al. Catalytic defluorinative [3 + 2] cycloaddition of trifluoromethylalkenes with alkynes via reduction of nickel(II) fluoride species. , 2015, Dalton transactions.
[3] K. Fuchibe,et al. Pinpoint-fluorinated phenanthrene synthesis based on CF bond activation of difluoroalkenes , 2015 .
[4] J. Aubé,et al. Intramolecular Friedel-Crafts Acylation Reaction Promoted by 1,1,1,3,3,3-Hexafluoro-2-propanol. , 2015, Organic letters.
[5] J. Ichikawa,et al. Method for the Synthesis of Dibenzo[g,p]Chrysenes: Domino Friedel-Crafts-Type Cyclization of Difluoroethenes Bearing Two Biaryl Groups. , 2015, Organic letters.
[6] T. Ichitsuka,et al. Nickel-Catalyzed Allylic C(sp3)–F Bond Activation of Trifluoromethyl Groups via β-Fluorine Elimination: Synthesis of Difluoro-1,4-dienes , 2015 .
[7] Jun Xu,et al. Pd-Catalyzed Regioselective Activation of gem-Difluorinated Cyclopropanes: A Highly Efficient Approach to 2-Fluorinated Allylic Scaffolds. , 2015, Angewandte Chemie.
[8] M. Harmata,et al. A Synthesis of Dihydrofuran-3(2H)-ones. , 2015, The Journal of organic chemistry.
[9] T. Loh,et al. Rhodium-catalysed C(sp2)–C(sp2) bond formation via C–H/C–F activation , 2015, Nature Communications.
[10] J. Wang,et al. Cu(I)-Catalyzed Cross-Coupling of Terminal Alkynes with Trifluoromethyl Ketone N-Tosylhydrazones: Access to 1,1-Difluoro-1,3-enynes. , 2015, Organic letters.
[11] Takao Saito,et al. Lewis Acid‐Catalyzed or Base‐Promoted Regioselective Cycloisomerization of N‐Imidoyl‐o‐alkynylanilines for Synthesis of N‐Imidoyl‐(1 H)‐indoles and 4‐Alkylidene‐3,4‐dihydroquinazolines , 2015 .
[12] M. Ohashi,et al. Copper-mediated One-pot Synthesis of Trifluorostyrene Derivatives from Tetrafluoroethylene and Arylboronate , 2015 .
[13] Samad Khaksar. Fluorinated alcohols: A magic medium for the synthesis of heterocyclic compounds , 2015 .
[14] Eden Gaster,et al. Significant enhancement in the efficiency and selectivity of iron-catalyzed oxidative cross-coupling of phenols by fluoroalcohols. , 2015, Angewandte Chemie.
[15] D. Hall,et al. A surprising substituent effect provides a superior boronic acid catalyst for mild and metal-free direct Friedel-Crafts alkylations and prenylations of neutral arenes. , 2015, Chemistry.
[16] K. Fuchibe,et al. Pinpoint-fluorinated phenacenes: new synthesis and solubility enhancement strategies. , 2015, Organic letters.
[17] T. Braun,et al. Functionalization of fluorinated molecules by transition-metal-mediated C-F bond activation to access fluorinated building blocks. , 2015, Chemical reviews.
[18] P. Champagne,et al. Friedel-Crafts reaction of benzyl fluorides: selective activation of C-F bonds as enabled by hydrogen bonding. , 2014, Angewandte Chemie.
[19] S. Cao,et al. Palladium- and nickel-catalyzed Kumada cross-coupling reactions of gem-difluoroalkenes and monofluoroalkenes with Grignard reagents. , 2014, The Journal of organic chemistry.
[20] T. Ichitsuka,et al. Double C-F bond activation through β-fluorine elimination: nickel-mediated [3+2] cycloaddition of 2-trifluoromethyl-1-alkenes with alkynes. , 2014, Angewandte Chemie.
[21] M. Hattori,et al. Nucleophilic 5-endo-trig Cyclization of 3,3-Difluoroallylic Metal Enolates and Enamides: Facile Synthesis of Ring-Fluorinated Dihydroheteroles , 2014, Synthesis.
[22] J. McNulty,et al. A Robust, Well-Defined Homogeneous Silver(I) Catalyst for Mild Intramolecular Hydroamination of 2-Ethynylanilines Leading to Indoles , 2014 .
[23] Jinbo Hu,et al. Copper-catalyzed gem-difluoroolefination of diazo compounds with TMSCF3 via C-F bond cleavage. , 2013, Journal of the American Chemical Society.
[24] M. Nieger,et al. Diastereoselective intramolecular allyl transfer from allyl carbamate accompanied by 5-endo-trig ring closure. , 2013, Angewandte Chemie.
[25] M. Hattori,et al. Nucleophilic 5-endo-trig Cyclization of 3,3-Difluoroallylic Ketone Enolates: Synthesis of 5-Fluorinated 2-Alkylidene-2,3-dihydrofurans , 2012, Synlett.
[26] G. Haufe,et al. C-F bond activation of unactivated aliphatic fluorides: synthesis of fluoromethyl-3,5-diaryl-2-oxazolidinones by desymmetrization of 2-aryl-1,3-difluoropropan-2-ols. , 2012, Angewandte Chemie.
[27] K. Fuchibe,et al. Domino Friedel-Crafts-type cyclizations of difluoroalkenes promoted by the α-cation-stabilizing effect of fluorine: an efficient method for synthesizing angular PAHs. , 2011, Chemistry.
[28] V. M. Kasture,et al. Total synthesis of natural cis-3-hydroxy-L-proline from D-glucose , 2010 .
[29] G. B. Bajracharya,et al. Pd-catalyzed 5-endo-trig-type cyclization of β,γ-unsaturated carbonyl compounds: an efficient ring closing reaction to give γ-butenolides and 3-pyrrolin-2-ones. , 2010, Chemical communications.
[30] T. Dohi,et al. Fluoroalcohols: versatile solvents in hypervalent iodine chemistry and syntheses of diaryliodonium(III) salts , 2010 .
[31] T. Hosokawa,et al. Efficient double bond migration of allylbenzenes catalyzed by Pd(OAc)2–HFIP system with unique substituent effect , 2010 .
[32] J. Ichikawa,et al. Transition-metal-catalyzed Electrophilic Activation of 1,1-Difluoro-1-alkenes : Oxindole Synthesis via Intramolecular Amination , 2010 .
[33] H. Isobe,et al. Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals. , 2009, Organic letters.
[34] H. Amii,et al. C-F bond activation in organic synthesis. , 2009, Chemical reviews.
[35] M. Murakami,et al. Synthesis of gem-Difluoroalkenes via β-Fluoride Elimination of Organorhodium(I) , 2008 .
[36] J. Ichikawa,et al. Efficient helicene synthesis: Friedel-Crafts-type cyclization of 1,1-difluoro-1-alkenes. , 2008, Angewandte Chemie.
[37] J. Ichikawa,et al. Activation of 1,1-difluoro-1-alkenes with a transition-metal complex: palladium(II)-catalyzed Friedel-Crafts-type cyclization of 4,4-(difluorohomoallyl)arenes. , 2007, Organic letters.
[38] A. Börner,et al. Fluorinated Alcohols as Solvents, Cosolvents and Additives in Homogeneous Catalysis , 2007 .
[39] J. Ichikawa,et al. 5-endo Heck-type cyclization of 2-(trifluoromethyl)allyl ketone oximes: Synthesis of 4-difluoromethylene-substituted 1-pyrrolines. , 2006, Chemical communications.
[40] M. Itonaga,et al. Friedel-Crafts-type cyclization of 2,2-difluorovinyl ketones via alpha-fluorocarbocations and its application in domino cyclizations. , 2006, Organic letters.
[41] J. Mihara,et al. Heck-type 5-endo-trig cyclizations promoted by vinylic fluorines: Ring-fluorinated indene and 3H-pyrrole syntheses from 1,1-difluoro-1-alkenes , 2006 .
[42] J. Mihara,et al. Heck-type 5-endo-trig cyclization promoted by vinylic fluorines: synthesis of 5-fluoro-3H-pyrroles. , 2005, Chemical communications.
[43] J. Ichikawa,et al. Friedel-Crafts Cyclization of 1,1-Difluoroalk-1-enes: Synthesis of Benzene-Fused Cyclic Ketones via α-Fluorocarbocations , 2004 .
[44] B. Crousse,et al. Fluorinated Alcohols: A New Medium for Selective and Clean Reaction , 2004 .
[45] A. Saito,et al. Carbocyclization reactions of terminally difluorinated alkenyl active methine compounds mediated by SnCl4 and amine , 2003 .
[46] J. Ichikawa,et al. The Nucleophilic 5-endo-trig Cyclization of 1,1-Difluoro-1-alkenes: Ring-Fluorinated Hetero- and Carbocycle Synthesis and Remarkable Effect of the Vinylic Fluorines on the Disfavored Process , 2002 .
[47] J. Ichikawa. Ring constructions by the use of fluorine substituent as activator and controller , 2000 .
[48] T. Okauchi,et al. Vinylic CF bond activation with low-valent zirconocene: the generation and cross-coupling reactions of 1-fluorovinylzirconocene , 1999 .
[49] T. Minami,et al. Fluorine-Directed Nazarov Cyclizations: A Controlled Synthesis of Cross-Conjugated 2-Cyclopenten-1-ones , 1995 .
[50] W. Heitz,et al. Synthesis of fluorostyrenes via palladium‐catalyzed reactions of aromatic halides with fluoroolefins , 1991 .
[51] M. Kolb,et al. An improved cyclisation protocol for the synthesis of δ,δ-difluoro-δ-lactones. , 1989 .
[52] M. Shiro,et al. Electrophilic cyclization reaction of gem-difluoroolefin derivatives: Syntheses of 6,6-difluorotetrahydro-2-pyrones and 2,2-difluorotetrahydropyran via halogen induced cyclization. , 1985 .
[53] M. Suda. Reactions of 1,1-difluoro-1-olefins with electrophilic reagents , 1980 .
[54] J. Baldwin,et al. Rules for ring closure. , 1977, Ciba Foundation symposium.
[55] G. Panda,et al. Intramolecular 5-endo-trig aminopalladation of β-hydroxy-γ-alkenylamine: efficient route to a pyrrolidine ring and its application for the synthesis of (−)-8,8a-di-epi-swainsonine , 2014 .
[56] M. Ohashi,et al. Catalytic Transformations of Fluorinated Olefins , 2014 .
[57] J. Baldwin,et al. 5-Endo-trigonal reactions: a disfavoured ring closure , 1976 .