Christmann, M. et al.: 2017 Science of Synthesis, 2017/2: Knowledge Updates 2017/2 DOI: 10.1055/sos-SD-140-00195
Knowledge Updates 2017/2

40.1.6.2 Azetidines (Update 2017)

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Buch

Herausgeber: Christmann, M.; Paquin, J.-F.; Weinreb, S. M.

Autoren: Couty, F.; Hunter, L.; Jubault, P.; Lectka, T.; Lequeux, T. P.; Pannecoucke, X.; Pitts, C. R.; Poisson, T.; Rodríguez-Morgade, M. S.; Rueda-Becerril, M.; Sammis, G. M.; Shibatomi, K.; Torres, T.; Yamazaki, T.

Titel: Knowledge Updates 2017/2

Print ISBN: 9783132414143; Online ISBN: 9783132414174; Buch-DOI: 10.1055/b-004-140262

Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie

Science of Synthesis Knowledge Updates



Übergeordnete Publikation

Titel: Science of Synthesis

DOI: 10.1055/b-00000101

Reihenherausgeber: Carreira, E. M.; Decicco, C. P.; Fürstner, A.; Koch, G.; Molander, G. A.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.

Typ: Mehrbändiges Werk

 


Abstract

This chapter is an update to the earlier Science of Synthesis contribution (Section 40.1.6) describing methods for the synthesis of azetidines. This review focuses on contributions in this field published between 2008 and 2015 (with some exceptions of papers published as early as 2006, which were not covered in the earlier review). This period has witnessed an impressive breakthrough of pharmaceutical agents bearing an azetidine ring in medicinal chemistry and the first examples of organocatalyzed enantioselective syntheses of nonracemic azetidines.

 
  • 4 Couty F, Drouillat B, Evano G, David O. Eur. J. Org. Chem. 2013; 2045
  • 6 Wuitschik G, Rogers-Evans M, Buckl A, Bernasconi M, Märki M, Godel T, Fischer H, Wagner B, Parilla I, Schuler F, Schneider J, Alker A, Schweizer WB, Müller K, Carreira EM. Angew. Chem. Int. Ed. 2008; 47: 4512
  • 10 Araújo N, Jenkinson SF, Martínez RF, Glawar AFG, Wormald MR, Butters TD, Nakagawa S, Adachi I, Kato A, Yoshihara A, Akimitsu K, Izumori K, Fleet GWJ. Org. Lett. 2012; 14: 4174
  • 25 Bouazaoui M, Martinez J, Cavelier F. Eur. J. Org. Chem. 2009; 2729
  • 27 Dekaris V, Reissig H.-U. Synlett 2010; 42
  • 28 Jasinski M, Moreno-Clavijo E, Reissig H.-U. Eur. J. Org. Chem. 2014; 442
  • 29 Yadav VK, Narhe BD, Kumar K, Hulikal V. Eur. J. Org. Chem. 2013; 4163
  • 30 Gerard B, Lee IV MD, Dandapani S, Duvall JR, Fitzgerald ME, Kesavan S, Lowe JT, Marié J.-C, Pandya BA, Suh B.-C, Welzel-O’Shea M, Dombrowski M, Hamann D, Lemercier B, Murillo T, Akella LB, Foley MA, Marcaurelle LA. J. Org. Chem. 2013; 78: 5160
  • 36 Feula A, Dhillon SS, Byravan R, Sangha M, Ebanks R, Salih MAH, Spencer N, Male L, Magyary I, Deng W.-P, Müller F, Fossey JS. Org. Biomol. Chem. 2013; 11: 5083
  • 43 Stanković S, Catak S, D’hooghe M, Goossens H, Abbaspour Tehrani K, Bogaert P, Waroquier M, Van Speybroeck V, De Kimpe N. J. Org. Chem. 2011; 76: 2157
  • 44 Lowe JT, Lee IV MD, Akella LB, Davoine E, Donckele EJ, Durak L, Duvall JR, Gerard B, Holson EB, Joliton A, Kesavan S, Lemercier BC, Liu H, Marié J.-C, Mulrooney CA, Muncipinto G, Welzel-O’Shea M, Panko LM, Rowley A, Suh B.-C, Thomas M, Wagner FF, Wei J, Foley MA, Marcaurelle LA. J. Org. Chem. 2012; 77: 7187
  • 46 Pizzonero M, Dupont S, Babel M, Beaumont S, Bienvenu N, Blanqué R, Cherel L, Christophe T, Crescenzi B, De Lemos E, Delerive P, Deprez P, De Vos S, Djata F, Fletcher S, Kopiejewski S, L’Ebraly C, Lefrançois J.-M, Lavazais S, Manioc M, Nelles L, Oste L, Polancec D, Qhénéhen V, Soulas F, Triballeau N, van der Aar E, Vandeghinste N, Wakselman E, Brys R, Saniere L. J. Med. Chem. 2014; 57: 10 044
  • 47 Drouillat B, d’Aboville E, Bourdreux F, Couty F. Eur. J. Org. Chem. 2014; 1103
  • 48 Faigl F, Kovács E, Turczel G, Szöllősy A, Mordini A, Balázs L, Holczbauer T, Czugler M. Tetrahedron: Asymmetry 2012; 23: 1607
  • 53 Bondada L, Rondla R, Pradere U, Liu P, Li C, Bobeck D, McBrayer T, Tharnish P, Courcambeck J, Halfon P, Whitaker T, Amblard F, Coats SJ, Schinazi RF. Bioorg. Med. Chem. Lett. 2013; 23: 6325
  • 68 Witulski B, Senft S, Bonet J, Jost O. Synthesis 2007; 243