Imido transfer of sulfonylimino-lambda3-bromane makes possible the synthesis of sulfonylimino-lambda3-iodanes.
暂无分享,去创建一个
[1] T. Okada,et al. Thermal and catalytic transylidations between halonium ylides and synthesis and reaction of stable aliphatic chloronium ylides. , 2008, Journal of the American Chemical Society.
[2] J. Chang,et al. Highly efficient ruthenium(II) porphyrin catalyzed amidation of aldehydes. , 2008, Angewandte Chemie.
[3] P. Müller,et al. Toward a synthetically useful stereoselective C-H amination of hydrocarbons. , 2008, Journal of the American Chemical Society.
[4] H. Chuman,et al. A new type of imido group donor: synthesis and characterization of sulfonylimino-lambda(3)-bromane that acts as a nitrenoid in the aziridination of olefins at room temperature under metal-free conditions. , 2007, Journal of the American Chemical Society.
[5] Zigang Li,et al. Gold(III)-catalyzed nitrene insertion into aromatic and benzylic C-H groups. , 2007, Journal of the American Chemical Society.
[6] K. W. Fiori,et al. Catalytic intermolecular amination of C-H bonds: method development and mechanistic insights. , 2007, Journal of the American Chemical Society.
[7] K. Miyamoto,et al. trans Influences on hypervalent bonding of aryl lambda(3)-iodanes: their stabilities and isodesmic reactions of benziodoxolones and benziodazolones. , 2006, Angewandte Chemie.
[8] M. M. Díaz‐Requejo,et al. Facile amine formation by intermolecular catalytic amidation of carbon-hydrogen bonds. , 2006, Journal of the American Chemical Society.
[9] C. Che,et al. Imido transfer from bis(imido)ruthenium(VI) porphyrins to hydrocarbons: effect of imido substituents, C-H bond dissociation energies, and Ru(VI/V) reduction potentials. , 2005, Journal of the American Chemical Society.
[10] C. Bolm,et al. Rhodium-catalyzed imination of sulfoxides and sulfides: efficient preparation of N-unsubstituted sulfoximines and sulfilimines. , 2004, Organic letters.
[11] P. Dauban,et al. Iminoiodanes and C-NBond Formation in Organic Synthesis , 2003 .
[12] P. Müller,et al. Enantioselective catalytic aziridinations and asymmetric nitrene insertions into CH bonds. , 2003, Chemical reviews.
[13] P. Stang,et al. Recent developments in the chemistry of polyvalent iodine compounds. , 2002, Chemical reviews.
[14] P. Dauban,et al. Copper-catalyzed nitrogen transfer mediated by iodosylbenzene PhI=O. , 2001, Journal of the American Chemical Society.
[15] C. Che,et al. Aziridination of alkenes and amidation of alkanes by bis(tosylimido)ruthenium(VI) porphyrins. A mechanistic study , 1999 .
[16] E. Skrzypczak‐Jankun,et al. A New Class of Iodonium Ylides Engineered as Soluble Primary Oxo and Nitrene Sources , 1999 .
[17] Scott A. Erickson,et al. 1-Amido-3-(1H)-1,2-benziodoxoles: Stable Amidoiodanes and Reagents for Direct Amidation of Organic Substrates. , 1997 .
[18] T. Umemoto. Electrophilic Perfluoroalkylating Agents. , 1996, Chemical reviews.
[19] P. Power,et al. Detailed Structural Characterization of the Polyvalent Iminoiodinanes ArINTs (Ar = C6H5 or 2,4,6-Me3C6H2; Ts = SO2C6H4-4-Me) and the Aryldichloroiodinane 2,4,6-i-Pr3C6H2ICl2 , 1995 .
[20] M. Ochiai,et al. Solvolysis of Cyclohexenyliodonium Salt, a New Precursor for the Vinyl Cation: Remarkable Nucleofugality of the Phenyliodonio Group and Evidence for Internal Return from an Intimate Ion-Molecule Pair , 1995 .
[21] M. Faul,et al. Development of the Copper-Catalyzed Olefin Aziridination Reaction , 1994 .
[22] S. Németh,et al. A new method for the preparation of (arylsulfonyliminoiodo)benzenes , 1993 .
[23] Corwin Hansch,et al. A survey of Hammett substituent constants and resonance and field parameters , 1991 .
[24] O. Prakash,et al. Capture of electron-deficient species with aryl halides. New syntheses of hypervalent iodonium ylides , 1985 .
[25] Yorinobu Yamada,et al. SYNTHESIS AND REACTION OF NEW TYPE I–N YLIDE, N-TOSYLIMINOIODINANE , 1975 .