Study of Sustainability and Scalability in the Cp*Rh(III)-Catalyzed Direct C–H Amidation with 1,4,2-Dioxazol-5-ones
暂无分享,去创建一个
[1] C. Siegel,et al. Process Development of a GCS Inhibitor Including Demonstration of Lossen Rearrangement on Kilogram Scale , 2015 .
[2] Sukbok Chang,et al. Mechanistic studies on the Rh(III)-mediated amido transfer process leading to robust C-H amination with a new type of amidating reagent. , 2015, Journal of the American Chemical Society.
[3] Sukbok Chang,et al. Transition-metal-catalyzed C-N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C-H amination. , 2015, Accounts of chemical research.
[4] Pitambar Patel,et al. Cobalt(III)-Catalyzed C–H Amidation of Arenes using Acetoxycarbamates as Convenient Amino Sources under Mild Conditions , 2015 .
[5] T. Laird. Editorial Reproducibility of Synthetic Results , 2014 .
[6] D. Musaev,et al. Comparative Investigations of Cp*-Based Group 9 Metal-Catalyzed Direct C–H Amination of Benzamides , 2014 .
[7] C. Bolm,et al. Methionine and Buthionine Sulfoximines: Syntheses under Mild and Safe Imidation/Oxidation Conditions , 2014 .
[8] J. Mahy,et al. Catalytic C-H amination: a reaction now accessible to engineered natural enzymes. , 2014, Angewandte Chemie.
[9] C. Bolm,et al. Light-induced ruthenium-catalyzed nitrene transfer reactions: a photochemical approach towards N-acyl sulfimides and sulfoximines. , 2014, Angewandte Chemie.
[10] F. Glorius,et al. Formal SN‐Type Reactions in Rhodium(III)‐Catalyzed CH Bond Activation , 2014 .
[11] Sukbok Chang,et al. Iridium-catalyzed C-H amination with anilines at room temperature: compatibility of iridacycles with external oxidants. , 2014, Journal of the American Chemical Society.
[12] Sukbok Chang,et al. Orthogonal reactivity of acyl azides in C-H activation: dichotomy between C-C and C-N amidations based on catalyst systems. , 2014, Organic letters.
[13] Sukbok Chang,et al. Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source. , 2014, Journal of the American Chemical Society.
[14] F. Patureau,et al. Oxidative C-H amination reactions. , 2014, Chemical Society reviews.
[15] Eberhard Guntrum,et al. Sanofi’s Solvent Selection Guide: A Step Toward More Sustainable Processes , 2013 .
[16] N. Chatani,et al. Catalytic functionalization of C(sp2)-H and C(sp3)-H bonds by using bidentate directing groups. , 2013, Angewandte Chemie.
[17] R. Sarpong,et al. Intramolecular C(sp3)–H amination , 2013 .
[18] Sukbok Chang,et al. Ir(III)-catalyzed mild C-H amidation of arenes and alkenes: an efficient usage of acyl azides as the nitrogen source. , 2013, Journal of the American Chemical Society.
[19] Sukbok Chang,et al. Ruthenium-catalyzed direct C-H amidation of arenes including weakly coordinating aromatic ketones. , 2013, Chemistry.
[20] F. Glorius,et al. Beyond directing groups: transition-metal-catalyzed C-H activation of simple arenes. , 2012, Angewandte Chemie.
[21] Junichiro Yamaguchi,et al. C-H bond functionalization: emerging synthetic tools for natural products and pharmaceuticals. , 2012, Angewandte Chemie.
[22] C. Bruneau,et al. Ruthenium(II)-catalyzed C-H bond activation and functionalization. , 2012, Chemical reviews.
[23] Ji Young Kim,et al. Rhodium-catalyzed intermolecular amidation of arenes with sulfonyl azides via chelation-assisted C-H bond activation. , 2012, Journal of the American Chemical Society.
[24] P. Yin,et al. Synthesis of 2,5-disubstituted oxazoles and oxazolines catalyzed by ruthenium(II) porphyrin and simple copper salts. , 2012, The Journal of organic chemistry.
[25] Fen Wang,et al. C-C, C-O and C-N bond formation via rhodium(III)-catalyzed oxidative C-H activation. , 2012, Chemical Society reviews.
[26] Sukbok Chang,et al. Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions. , 2012, Organic letters.
[27] Trevor Laird,et al. Green Chemistry is Good Process Chemistry , 2012 .
[28] T. Ramirez,et al. Recent advances in transition metal-catalyzed sp3 C-H amination adjacent to double bonds and carbonyl groups. , 2012, Chemical Society reviews.
[29] Sukbok Chang,et al. Intermolecular oxidative C-N bond formation under metal-free conditions: control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation. , 2011, Journal of the American Chemical Society.
[30] Ji Young Kim,et al. Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation. , 2011, Chemical Society reviews.
[31] Concepción Jiménez-González,et al. Using the Right Green Yardstick: Why Process Mass Intensity Is Used in the Pharmaceutical Industry To Drive More Sustainable Processes , 2011 .
[32] Concepción Jiménez-González,et al. Expanding GSK's solvent selection guide ― embedding sustainability into solvent selection starting at medicinal chemistry , 2011 .
[33] P. Baran,et al. If C-H bonds could talk: selective C-H bond oxidation. , 2011, Angewandte Chemie.
[34] Sukbok Chang,et al. Intramolecular oxidative C-N bond formation for the synthesis of carbazoles: comparison of reactivity between the copper-catalyzed and metal-free conditions. , 2011, Journal of the American Chemical Society.
[35] M. Gaunt,et al. Recent developments in natural product synthesis using metal-catalysed C-H bond functionalisation. , 2011, Chemical Society reviews.
[36] P. Dauban,et al. Catalytic C-H amination: the stereoselectivity issue. , 2011, Chemical Society reviews.
[37] Daniel Morton,et al. Guiding principles for site selective and stereoselective intermolecular C-H functionalization by donor/acceptor rhodium carbenes. , 2011, Chemical Society reviews.
[38] C. Yeung,et al. Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds. , 2011, Chemical reviews.
[39] T. Laird. Safety Special Section Editorial , 2010 .
[40] James C. Collins,et al. Direct azole amination: C-H functionalization as a new approach to biologically important heterocycles. , 2010, Angewandte Chemie.
[41] J. Ellman,et al. Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation. , 2010, Chemical reviews.
[42] Chang-Liang Sun,et al. Pd-catalyzed oxidative coupling with organometallic reagents via C-H activation. , 2010, Chemical communications.
[43] Michael G. Vetelino,et al. Carbonyldiimidazole-mediated Lossen rearrangement. , 2009, Organic letters.
[44] P. Dauban,et al. Catalytic C-H amination: recent progress and future directions. , 2009, Chemical communications.
[45] Peter J. Dunn,et al. Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation , 2008 .
[46] Trevor Laird,et al. How Safe Are Your Reactions , 2004 .
[47] Hiroshi Iwamura,et al. Amplification of enantiomeric excess in a proline-mediated reaction. , 2004, Angewandte Chemie.
[48] Concepción Jiménez-González,et al. Expanding GSK’s Solvent Selection Guide—application of life cycle assessment to enhance solvent selections , 2004 .
[49] J. Bercaw,et al. Understanding and exploiting C–H bond activation , 2002, Nature.
[50] D. Ende,et al. A Calorimetric Investigation To Safely Scale-Up a Curtius Rearrangement of Acryloyl Azide , 1998 .
[51] Linda D. Tuma. Identification of a safe diazotransfer reagent , 1994 .
[52] L. Bretherick,et al. Bretherick's Handbook of Reactive Chemical Hazards , 1990 .
[53] E. Scriven,et al. Azides: their preparation and synthetic uses , 1988 .
[54] J. Sauer,et al. Konkurrenzexperimente zum nachweis von acylnitrenen , 1987 .
[55] W. Middleton. 1,3,4-Dioxazol-2-ones: a potentially hazardous class of compounds , 1983 .
[56] L. Bauer,et al. The Chemistry of Hydroxamic Acids and N‐Hydroxyimides , 1974 .
[57] J. Sauer,et al. Acylnitrene als zwischenstufen bei der photolyse Fünfgliedriger heterocyclen , 1974 .
[58] J. Sauer,et al. Thermolyse und photolyse von 3.4-Diphenyl-Δ 2-1.2.4-oxdiazolinon-(5) und 2.4-Diphenyl- Δ2-1.3.4-Oxdiazolinon-(5) , 1968 .
[59] J. Sauer,et al. Thermolyse und photolyse von 3-subtituierten Δ2- 1.4.2-dioxazolinonen-(5), Δ2-1.4.2-dioxazolin-thionen-(5) und 4-substituierten Δ3-1.2.5.3-thiadioxazolin-s-oxiden , 1968 .
[60] H. L. Yale. The Hydroxamic Acids. , 1943 .
[61] Theodor Curtius. 20. Hydrazide und Azide organischer Säuren I. Abhandlung , 1894 .
[62] Theodor Curtius. Ueber Stickstoffwasserstoffsäure (Azoimid) N3H , 1890 .
[63] W. Lossen. Ueber die Structurformel des Hydroxylamins und seiner amidartigen Derivate , 1875 .
[64] W. Lossen. Ueber Benzoylderivate des Hydroxylamins , 1872 .
[65] Heinrick Lossen. Ueber die Oxalohydroxamsäure , 1869 .