Campagne, J.-M.  et al.: 2024 Science of Synthesis, 2024/3: Knowledge Updates 2024/3 DOI: 10.1055/sos-SD-120-00303
Knowledge Updates 2024/3

20.2.1.3.6 Synthesis of Carboxylic Acids from Aldehydes and Ketones (Update 2024)

Weitere Informationen

Buch

Herausgeber: Campagne, J.-M. ; Donohoe, T. J.; Drabowicz, J. ; Fuerstner, A. ; Jiang, X. ; Wang, M. ; Wirth, T.

Autoren: Durandetti, M. ; Fan, Q. ; Favre-Réguillon, A. ; Franck, X. ; Gulder, T. ; Kiełbasiński, P. ; Kretzschmar, M. ; Kwiatkowska, M. ; Kwiecień, H. U.; Leclerc, E. ; Marciniszyn, J. P.; Mita, T. ; Rawat, V. K. ; Walker, J. C. L. ; Zhu, H.

Titel: Knowledge Updates 2024/3

Online ISBN: 9783132457089; Buch-DOI: 10.1055/b000000969

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: 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.

Typ: Mehrbändiges Werk

 


Abstract

This chapter is an update to the earlier Science of Synthesis contribution (Section 20.2.1.3) and describes methods for the formation of carboxylic acids reported in the period 2007–2023. The focus is on recent advances in the synthetic preparations of carboxylic acids from aldehydes and ketones using green and sustainable reagents as well as continuous flow procedures.

 
  • 2 Cook DC, Jones RH, Kabir H, Lythgoe DJ, McFarlane IM, Pemberton C, Thatcher AA, Thompson DM, Walton JB. Org. Process Res. Dev. 1998; 2: 157
  • 21 Fang X, Bandarage UK, Wang T, Schroeder JD, Garvey DS. Synlett 2003; 489
  • 25 Kürti L, Czako B. Strategic Applications of Named Reactions in Organic Synthesis. Elsevier; Amsterdam 2005
  • 36 Horn A, Kazmaier U. Eur. J. Org. Chem. 2018; 2531
  • 40 Kubitschke J, Lange H, Strutz H In: Ullmann’s Encyclopedia of Industrial Chemistry online 7th ed., Wiley-VCH Weinheim, Germany 2014; DOI:
  • 60 Moureu C, Chaux R. Org. Synth., Coll. Vol. I 1941; 166
  • 64 García G, Solano I, Sánchez G, Santana MD, López G, Casabó J, Molins E, Miravitlles C. J. Organomet. Chem. 1994; 467: 119
  • 70 Douthwaite M, Huang X, Iqbal S, Miedziak PJ, Brett GL, Kondrat SA, Edwards JK, Sankar M, Knight DW, Bethell D, Hutchings GJ. Catal. Sci. Technol. 2017; 7: 5284
  • 79 Burglova K, Okorochenkov S, Budesinsky M, Hlavac J. Eur. J. Org. Chem. 2017; 389
  • 80 Könst P, Merkens H, Kara S, Kochius S, Vogel A, Zuhse R, Holtmann D, Arends IWCE, Hollmann F. Angew. Chem. Int. Ed. 2012; 51: 9914 corrigendum: Angew. Chem. Int. Ed. 2012; 51: 11 924
  • 86 Biewenga L, Saravanan T, Kunzendorf A, van der Meer J.-Y, Pijning T, Tepper PG, van Merkerk R, Charnock SJ, Thunnissen A.-MWH, Poelarends GJ. ACS Catal. 2019; 9: 1503
  • 107 Shaikh TMA, Sudalai A. Eur. J. Org. Chem. 2008; 4877