Copper-catalyzed tandem aerobic oxidative cyclization for the synthesis of 4-cyanoalkylpyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclobutanone oxime esters.
暂无分享,去创建一个
Rulong Yan | Zhenyu An | Yong Jiang | X. Guan
[1] W. Xiao,et al. Photoredox-promoted alkyl radical addition/semipinacol rearrangement sequences of alkenylcyclobutanols: rapid access to cyclic ketones. , 2018, Chemical communications.
[2] C. Corminboeuf,et al. Fine-tuned organic photoredox catalysts for fragmentation-alkynylation cascades of cyclic oxime ethers† †Electronic supplementary information (ESI) available: Experimental and computational data. CCDC 1052646 and 1838186. For ESI and crystallographic data in CIF or other electronic format see DOI: 1 , 2018, Chemical science.
[3] Xinhua Duan,et al. Iron‐Catalyzed Ring‐Opening/Allylation of Cyclobutanone Oxime Esters with Allylic Sulfones , 2018 .
[4] Xinhua Duan,et al. Redox-Neutral Cyanoalkylation/Cyclization of Olefinic 1,3-Dicarbonyls with Cycloketone Oxime Esters: Access to Cyanoalkylated Dihydrofurans. , 2018, The Journal of organic chemistry.
[5] Xiao‐Ye Yu,et al. A Visible-Light-Driven Iminyl Radical-Mediated C-C Single Bond Cleavage/Radical Addition Cascade of Oxime Esters. , 2018, Angewandte Chemie.
[6] S. Castle,et al. Synthesis of Functionalized Nitriles by Microwave-Promoted Fragmentations of Cyclic Iminyl Radicals. , 2018, Chemistry.
[7] Zhong-Ling Lu,et al. Cu-Catalyzed Redox-Neutral Ring Cleavage of Cycloketone O-Acyl Oximes: Chemodivergent Access to Distal Oxygenated Nitriles. , 2018, Organic letters.
[8] Silong Xu,et al. Copper-Catalyzed Redox-Neutral Cyanoalkylarylation of Activated Alkenes with Cyclobutanone Oxime Esters. , 2017, The Journal of organic chemistry.
[9] James J. Douglas,et al. Photoinduced Remote Functionalisations by Iminyl Radical Promoted C−C and C−H Bond Cleavage Cascades , 2017, Angewandte Chemie.
[10] Xinhua Duan,et al. Direct C-H Cyanoalkylation of Heteroaromatic N-Oxides and Quinones via C-C Bond Cleavage of Cyclobutanone Oximes. , 2017, Organic letters.
[11] D. Leonori,et al. Synthesis of Arylamines via Aminium Radicals , 2017, Angewandte Chemie.
[12] Rulong Yan,et al. FeCl3-Catalyzed synthesis of pyrrolo[1,2-a]quinoxaline derivatives from 1-(2-aminophenyl)pyrroles through annulation and cleavage of cyclic ethers. , 2017, Chemical communications.
[13] Lei Zhou,et al. Visible-light promoted γ-cyanoalkyl radical generation: three-component cyanopropylation/etherification of unactivated alkenes. , 2017, Chemical communications.
[14] Zhuangzhi Shi,et al. Copper-Catalyzed Intermolecular Heck-Like Coupling of Cyclobutanone Oximes Initiated by Selective C-C Bond Cleavage. , 2017, Angewandte Chemie.
[15] A. Studer,et al. Iminyl-Radicals by Oxidation of α-Imino-oxy Acids: Photoredox-Neutral Alkene Carboimination for the Synthesis of Pyrrolines. , 2017, Angewandte Chemie.
[16] D. Leonori,et al. Photoredox Imino Functionalizations of Olefins , 2017, Angewandte Chemie.
[17] Nicklas Selander,et al. Divergent Iron-Catalyzed Coupling of O-Acyloximes with Silyl Enol Ethers. , 2017, Chemistry.
[18] Lei Feng,et al. Efficient synthesis of pyrrolo[1,2-a]quinoxalines catalyzed by a Brønsted acid through cleavage of C-C bonds. , 2016, Organic & biomolecular chemistry.
[19] V. Kaplum,et al. Synthesis and biological evaluation of novel 2,3-disubstituted quinoxaline derivatives as antileishmanial and antitrypanosomal agents. , 2015, European journal of medicinal chemistry.
[20] S. Castle,et al. Microwave-promoted tin-free iminyl radical cyclization with TEMPO trapping: a practical synthesis of 2-acylpyrroles. , 2015, Organic letters.
[21] I. Marek,et al. Selective carbon-carbon bond cleavage for the stereoselective synthesis of acyclic systems. , 2015, Angewandte Chemie.
[22] Hong Xia,et al. Design of D–A–π–A organic dyes with different acceptor and auxiliary acceptor for highly efficient dye-sensitized solar cells: a computational study , 2014 .
[23] Aurélien Lesnard,et al. Synthesis and in vitro evaluation of 4-trichloromethylpyrrolo[1,2-a]quinoxalines as new antiplasmodial agents. , 2014, European journal of medicinal chemistry.
[24] Martin D. Eastgate,et al. A Mild, Ferrocene-Catalyzed C–H Imidation of (Hetero)Arenes , 2014, Journal of the American Chemical Society.
[25] J. Jose,et al. Synthesis and biological evaluation of novel substituted pyrrolo[1,2-a]quinoxaline derivatives as inhibitors of the human protein kinase CK2. , 2013, European journal of medicinal chemistry.
[26] N. Cramer,et al. Cyclobutanes in catalysis. , 2011, Angewandte Chemie.
[27] A. Monge,et al. New 1,4-di-N-oxide-quinoxaline-2-ylmethylene isonicotinic acid hydrazide derivatives as anti-Mycobacterium tuberculosis agents. , 2011, Bioorganic & medicinal chemistry letters.
[28] E. Novellino,et al. Novel, potent, and selective quinoxaline-based 5-HT(3) receptor ligands. 1. Further structure-activity relationships and pharmacological characterization. , 2009, Journal of medicinal chemistry.
[29] F. Pinguet,et al. In vitro and in vivo anti-tumoral activities of imidazo[1,2-a]quinoxaline, imidazo[1,5-a]quinoxaline, and pyrazolo[1,5-a]quinoxaline derivatives. , 2008, Bioorganic & medicinal chemistry.
[30] C. Jarry,et al. Synthesis of New Pyrrolo[1,2-a]quinoxaline Derivatives as Potential Inhibitors of Akt Kinase , 2008, Journal of enzyme inhibition and medicinal chemistry.
[31] T. Nishimura,et al. Iridium-catalyzed ring cleavage reaction of cyclobutanone O-benzoyloximes providing nitriles. , 2005, Organic letters.
[32] T. Nishimura,et al. Palladium-catalyzed transformation of cyclobutanone O-benzoyloximes to nitriles via C-C bond cleavage. , 2004, The Journal of organic chemistry.
[33] C. Sergheraert,et al. Synthesis, antimalarial activity, and molecular modeling of new pyrrolo[1,2-a]quinoxalines, bispyrrolo[1,2-a]quinoxalines, bispyrido[3,2-e]pyrrolo[1,2-a]pyrazines, and bispyrrolo[1,2-a]thieno[3,2-e]pyrazines. , 2004, Journal of medicinal chemistry.
[34] O. Kulinkovich. The chemistry of cyclopropanols. , 2003, Chemical reviews.
[35] E Novellino,et al. Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent. , 2001, Journal of medicinal chemistry.
[36] S. Uemura,et al. Palladium(0)-Catalyzed Ring Cleavage of Cyclobutanone Oximes Leading to Nitriles via β-Carbon Elimination , 2000 .
[37] P. Renard,et al. Synthesis of new pyrrolo(1,2-a)quinoxalines: potential non-peptide glucagon receptor antagonists , 1998 .
[38] M. Hamon,et al. Novel and highly potent 5-HT3 receptor agonists based on a pyrroloquinoxaline structure. , 1997, Journal of medicinal chemistry.
[39] P Delagrange,et al. Novel and selective partial agonists of 5-HT3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines. , 1997, Journal of medicinal chemistry.
[40] S. Zard,et al. Iminyl radicals: part II. ring opening of cyclobutyl- and cyclopentyliminyl radicals. , 1994 .
[41] S. Zard,et al. Ring opening induced by iminyl radicals derived from cyclobutanones: new aspects of tin hydride cleavage of S-phenyl sulfenylimines , 1991 .