Bagley, M. C. et al.: 2019 Science of Synthesis, 2019/1: Knowledge Updates 2019/1 DOI: 10.1055/sos-SD-115-00651
Knowledge Updates 2019/1

15.5.4 Isoquinolines (Update 2019)

More Information

Book

Editors: Bagley, M. C.; Banert, K.; Krause, N.; Yus, M.

Authors: Celik, I.; Eames, J.; Garrido, N. M.; Hummel, S.; Kirsch, S. F.; Nieto, C. T.; Pilgrim, B. S.; Podlech, J.; Tucker, M. J.

Title: Knowledge Updates 2019/1

Print ISBN: 9783132429598; Online ISBN: 9783132429628; Book DOI: 10.1055/b-006-166042

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Knowledge Updates



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Type: Multivolume Edition

 


Abstract

This chapter is an update to the earlier Science of Synthesis contributions (Sections 15.5.1, 15.5.2, and 15.5.3) covering the synthesis and reactivity of isoquinolines, isoquinoline Noxides, and isoquinolinium salts. It focuses on the literature published in the period 2003–2016, with a particular emphasis on transition-metal-catalyzed synthetic processes.

 
  • 12 Mancini GBJ, Henry GC, Macaya C, O'Neill BJ, Pucillo AL, Carere RG, Wargovich TJ, Mudra H, Lüscher TF, Klibaner MI, Haber HE, Uprichard ACG, Pepine CJ, Pitt B. Circulation 1996; 94: 258
  • 13 Wu SC, Yoon D, Chin J, van Kirk K, Seethala R, Golla R, He B, Harrity T, Kunselman LK, Morgan NN, Ponticiello RP, Taylor JR, Zebo R, Harper TW, Li W, Wang M, Zhang L, Sleczka BG, Nayeem A, Sheriff S, Camac DM, Morin PE, Everlof JG, Li Y.-X, Ferraro CA, Kieltyka K, Shou W, Vath MB, Zvyaga TA, Gordon DA, Robl JA. Bioorg. Med. Chem. Lett. 2011; 21: 6693
  • 14 Kashiwada Y, Aoshima A, Ikeshiro Y, Chen Y.-P, Furukawa H, Itoigawa M, Fujioka T, Mihashi K, Cosentino LM, Morris-Natschke SL, Lee K.-H. Bioorg. Med. Chem. 2005; 13: 443
  • 18 Tsuboyama A, Iwawaki H, Furugori M, Mukaide T, Kamatani J, Igawa S, Moriyama T, Miura S, Takiguchi T, Okada S, Hoshino M, Ueno K. J. Am. Chem. Soc. 2003; 125: 12 971
  • 22 Ho C.-L, Wong W.-Y, Gao Z.-Q, Chen C.-H, Cheah K.-W, Yao B, Xie Z.-Y, Wang Q, Ma D.-G, Wang L.-X, Yu X.-M, Kwok H.-S, Lin Z.-Y. Adv. Funct. Mater. 2008; 18: 319
  • 29 Fischer A, Galloway WJ, Vaughan J. J. Chem. Soc. 1964; 3591
  • 31 Ford A, Sinn E, Woodward S. J. Chem. Soc., Perkin Trans. 1 1997; 927
  • 34 Dewar MJS, Maitlis PM. J. Chem. Soc. 1957; 2521
  • 36 Katritzky AR, Ramsden CA, Joule JA, Zhdankin VV. Handbook of Heterocyclic Chemistry. Elsevier; Oxford 2010
  • 43 Ohta Y, Oishi S, Fujii N, Ohno H. Chem. Commun. (Cambridge) 2008; 835
  • 51 Martínez AG, Fernández AH, Vilchez DM, Gutiérrez MLL, Subramanian LR. Synlett 1993; 229
  • 52 Kitamura T, Kobayashi S, Taniguchi H. Chem. Lett. 1984; 1351
  • 53 Sato T, Tamura K, Nagayoshi K. Chem. Lett. 1983; 791
  • 54 Ahmad S, Whalley WB, Jones DF. J. Chem. Soc. C 1971; 3590
  • 63 Fukutani T, Umeda N, Hirano K, Satoh T, Miura M. Chem. Commun. (Cambridge) 2009; 5141
  • 111 Dunetz JR, Ciccolini RP, Fröling M, Paap SM, Allen AJ, Holmes AB, Tester JW, Danheiser RL. Chem. Commun. (Cambridge) 2005; 4465
  • 133 Ye S, Wang H, Wu J. Eur. J. Org. Chem. 2010; 6436
  • 139 Boyd DR, Sharma ND, Dorrity MRJ, Hand MV, McMordie RAS, Malone JF, Porter HP, Dalton H, Chima J, Sheldrake GN. J. Chem. Soc., Perkin Trans. 1 1993; 1065
  • 156 Vaccari D, Davoli P, Ori C, Spaggiari A, Prati F. Synlett 2008; 2807
  • 165 Palacios F, Alonso C, Rodríguez M, Martínez de Marigorta E, Rubiales G. Eur. J. Org. Chem. 2005; 1795
  • 169 Iwayama T, Sato Y. Chem. Commun. (Cambridge) 2009; 5245
  • 178 Reyes-Sánchez A, Cañavera-Buelvas F, Barrios-Francisco R, Cifuentes-Vaca OL, Flores-Alamo M, García JJ. Organometallics 2011; 30: 3340
  • 188 Přech J, Václavík J, Šot P, Pecháček J, Vilhanová B, Januščák J, Syslová K, Pažout R, Maixner J, Zápal J, Kuzma M, Kačer P. Catal. Commun. 2013; 36: 67
  • 189 Pecháček J, Václavík J, Přech J, Šot P, Januščák J, Vilhanová B, Vavřík J, Kuzma M, Kačer P. Tetrahedron: Asymmetry 2013; 24: 233
  • 190 Wu J, Wang F, Ma Y, Cui X, Cun L, Zhu J, Deng J, Yu B. Chem. Commun. (Cambridge) 2006; 1766
  • 230 Fajardo V, Araya M, Cuadra P, Oyarzun A, Gallardo A, Cueto M, Diaz-Marrero AR, Darias J, Villarroel L, Álvarez C, Mora-Pérez Y, Joseph-Nathan P. J. Nat. Prod. 2009; 72: 1355
  • 240 Yeom H.-S, Kim S, Shin S. Synlett 2008; 924
  • 243 Campeau L.-C, Stuart DR, Leclerc J.-P, Bertrand-Laperle M, Villemure E, Sun H.-Y, Lasserre S, Guimond N, Lecavallier M, Fagnou K. J. Am. Chem. Soc. 2009; 131: 3291