Iodine-Catalyzed Oxidative Functionalization of Azaarenes with Benzylic C(sp(3))-H Bonds via N-Alkylation/Amidation Cascade: Two-Step Synthesis of Isoindolo[2,1-b]isoquinolin-7(5H)-one.
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[1] Li-Xia Wang,et al. Iodine‐Catalyzed Oxidative Benzylic C−H Bond Amination of Azaarenes: Practical Synthesis of Quinazolin‐4(3 H)‐ones , 2016 .
[2] A. Bridoux,et al. Expeditious Synthesis of the Topoisomerase I Inhibitors Isoindolo[2,1-b]isoquinolin-7(5H)-one and the Alkaloid Rosettacin Based on Aryl Radical Cyclization of Enamide Generated by Using N-Acyliminium Chemistry , 2015 .
[3] T. Wen,et al. Construction of Isoquinolin‐1(2H)‐ones by Copper‐Catalyzed Tandem Reactions of 2‐(1‐Alkynyl)benzaldimines with Water , 2015 .
[4] K. Sun,et al. Regioselective, Molecular Iodine-Mediated C3 Iodination of Quinolines. , 2015, Organic letters.
[5] Yalin Tang,et al. Copper‐Catalyzed Intramolecular C–C Bond Cleavage To Construct 2‐Substituted Quinazolinones , 2015 .
[6] Luo Yang,et al. Metal‐Free Oxidative Decarbonylative Coupling of Aliphatic Aldehydes with Azaarenes: Successful Minisci‐Type Alkylation of Various Heterocycles , 2015 .
[7] Dong Liu,et al. Iodine-catalyzed oxidative coupling reactions utilizing C - H and X - H as nucleophiles. , 2015, Chemistry, an Asian journal.
[8] Xiaoqiang Yu,et al. Isoquinolone synthesis through S(N)Ar reaction of 2-halobenzonitriles with ketones followed by cyclization. , 2015, The Journal of organic chemistry.
[9] Nicola J. Webb,et al. Rhodium(III)-catalyzed C-H activation/annulation with vinyl esters as an acetylene equivalent. , 2014, Organic letters.
[10] A. Antonchick,et al. Organocatalytic oxidative annulation of benzamide derivatives with alkynes. , 2014, Angewandte Chemie.
[11] Feng Zhang,et al. Brønsted acid catalyzed benzylic C-H bond functionalization of azaarenes: nucleophilic addition to nitroso compounds. , 2014, Organic letters.
[12] Shun-Yi Wang,et al. Synthesis of isatins by I2/TBHP mediated oxidation of indoles. , 2014, Organic letters.
[13] G. Deng,et al. C(sp3)–C(sp3) bond formation via copper/Brønsted acid co-catalyzed C(sp3)–H bond oxidative cross-dehydrogenative-coupling (CDC) of azaarenes , 2014 .
[14] Wenlong Wei,et al. Recent Advances in Iodine-Mediated Organic Reactions , 2014 .
[15] T. Rovis,et al. Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes. , 2014, Synlett : accounts and rapid communications in synthetic organic chemistry.
[16] Yixiang Cheng,et al. Synthesis of functionalized isoquinolin-1(2H)-ones by copper-catalyzed α-arylation of ketones with 2-halobenzamides. , 2013, Chemistry.
[17] Luo Yang,et al. Brønsted acid promoted benzylic C-H bond functionalization of azaarenes: nucleophilic addition to aldehydes. , 2012, Organic & biomolecular chemistry.
[18] F. Glorius,et al. Mild Rh(III)-catalyzed C-H activation and annulation with alkyne MIDA boronates: short, efficient synthesis of heterocyclic boronic acid derivatives. , 2012, Journal of the American Chemical Society.
[19] Cheol‐Min Park,et al. Rhodium(III)-catalyzed intramolecular annulation through C-H activation: total synthesis of (±)-antofine, (±)-septicine, (±)-tylophorine, and rosettacin. , 2012, Angewandte Chemie.
[20] F. Glorius,et al. Mild rhodium(III)-catalyzed C-H activation and intermolecular annulation with allenes. , 2012, Angewandte Chemie.
[21] J. Ellman,et al. Rhodium catalyzed chelation-assisted C-H bond functionalization reactions. , 2012, Accounts of chemical research.
[22] 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.
[23] L. Ackermann,et al. Ruthenium-catalyzed C-H/N-O bond functionalization: green isoquinolone syntheses in water. , 2011, Organic letters.
[24] Baiquan Wang,et al. Ruthenium-catalyzed isoquinolone synthesis through C-H activation using an oxidizing directing group. , 2011, Chemistry.
[25] Nicolas Guimond,et al. Rhodium(III)-catalyzed heterocycle synthesis using an internal oxidant: improved reactivity and mechanistic studies. , 2011, Journal of the American Chemical Society.
[26] F. Glorius,et al. Rhodium-catalyzed oxidative olefination of C-H bonds in acetophenones and benzamides. , 2011, Angewandte Chemie.
[27] W. Cho,et al. 3-Arylisoquinolines as novel topoisomerase I inhibitors. , 2011, Bioorganic & medicinal chemistry.
[28] R. Crabtree,et al. Rh-catalyzed oxidative coupling between primary and secondary benzamides and alkynes: synthesis of polycyclic amides. , 2010, The Journal of organic chemistry.
[29] T. Rovis,et al. Rhodium-catalyzed oxidative cycloaddition of benzamides and alkynes via C-H/N-H activation. , 2010, Journal of the American Chemical Society.
[30] K. Parthasarathy,et al. Synthesis of highly substituted isoquinolone derivatives by nickel-catalyzed annulation of 2-halobenzamides with alkynes. , 2010, Organic letters.
[31] K. Hirano,et al. Rhodium-catalyzed Oxidative Coupling/Cyclization of Benzamides with Alkynes via C-H Bond Cleavage , 2010 .
[32] Nicolas Guimond,et al. Rhodium(III)-catalyzed isoquinolone synthesis: the N-O bond as a handle for C-N bond formation and catalyst turnover. , 2010, Journal of the American Chemical Society.
[33] S. Ducki,et al. Antineoplastic agents. 454. Synthesis of the strong cancer cell growth inhibitors trans-dihydronarciclasine and 7-deoxy-trans-dihydronarciclasine (1a). , 2009, Journal of natural products.
[34] Y. Pommier. DNA topoisomerase I inhibitors: chemistry, biology, and interfacial inhibition. , 2009, Chemical reviews.
[35] W. Cho,et al. Structural modification of 3-arylisoquinolines to isoindolo[2,1-b]isoquinolinones for the development of novel topoisomerase 1 inhibitors with molecular docking study. , 2009, Bioorganic & medicinal chemistry letters.
[36] Y. Pommier,et al. Design, synthesis, and biological evaluation of 14-substituted aromathecins as topoisomerase I inhibitors. , 2008, Journal of medicinal chemistry.
[37] Toshimasa Tanaka,et al. Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (2). , 2008, Bioorganic & medicinal chemistry.
[38] Dinesh Kumar,et al. Tandem C-C coupling--intramolecular acetylenic Schmidt reaction under Pd/C-Cu catalysis. , 2007, Chemical communications.
[39] Y. Pommier. Topoisomerase I inhibitors: camptothecins and beyond , 2006, Nature Reviews Cancer.
[40] D. L. Herald,et al. Isolation and structural modification of 7-deoxynarciclasine and 7-deoxy-trans-dihydronarciclasine. , 2006, Journal of natural products.
[41] G. Pettit,et al. Antineoplastic agents. 527. Synthesis of 7-deoxynarcistatin, 7-deoxy-trans-dihydronarcistatin, and trans-dihydronarcistatin 1(1). , 2005, Journal of natural products.
[42] S. Hecht,et al. 14-azacamptothecin: a potent water-soluble topoisomerase I poison. , 2005, Journal of the American Chemical Society.
[43] V. A. Glushkov,et al. Synthesis of 1(2H)-Isoquinolones. (Review) , 2001 .
[44] R. Ferone,et al. Folate analogues. 35. Synthesis and biological evaluation of 1-deaza, 3-deaza, and bridge-elongated analogues of N10-propargyl-5,8-dideazafolic acid. , 1991, Journal of medicinal chemistry.
[45] S. Yoshifuji,et al. Ruthenium Tetroxide Oxidation of 3, 4-Dihydroisoquinolin-1(2H)-ones : An Efficient Synthesis of Isoquinoline-1, 3, 4(2H)-triones , 1989 .
[46] John Godfry. Communications- Novel Synthesis of a 1,2,5,6-Dibenzocycl[3,2,2]azine , 1959 .