To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Reissert reaction

From Wikipedia, the free encyclopedia

Reissert reaction
Named after Arnold Reissert
Reaction type Addition reaction

The Reissert reaction is a series of chemical reactions that transforms quinoline to quinaldic acid.[1][2] Quinolines will react with acid chlorides and potassium cyanide to give 1-acyl-2-cyano-1,2-dihydroquinolines, also known as Reissert compounds. Hydrolysis gives the desired quinaldic acid.

The Reissert reaction
The Reissert reaction

The Reissert reaction is also successful with isoquinolines[3][4] and most pyridines.

Several reviews have been published.[5][6]

YouTube Encyclopedic

  • 1/2
    Views:
    3 059
    1 067
  • Fischer Indole Synthesis
  • Mod-28 Lec-32 Indole Synthesis - I

Transcription

References

  1. ^ Reissert, Arnold (1905). "Ueber die Einführung der Benzoyl-gruppe in tertiäre cyclische Basen". Berichte der deutschen chemischen Gesellschaft. 38 (2): 1603–1614. doi:10.1002/cber.19050380260.
  2. ^ Grosheintz, J. M.; Fischer, Hermann O. L. (1941). "Preparation of 1-Acyl-1,2-dihydroquinaldonitriles and their Hydrolysis to Aldehydes". Journal of the American Chemical Society. 63 (7): 2021–2022. doi:10.1021/ja01852a066.
  3. ^ Weinstock, J.; Boekelheide, V. Organic Syntheses, Coll. Vol. 4, p. 641 (1963); Vol. 38, p. 58 (1958). (Article)
  4. ^ Uff, B. C.; Kershaw, J. R.; Neumeyer, J. L. Organic Syntheses, Coll. Vol. 6, p. 115 (1988); Vol. 56, p. 19 (1977). (Article)
  5. ^ Mosettig, E. Org. React. 1954, 8, 220. (Review)
  6. ^ McEwen, William E.; Cobb, R. Lynn (1955). "The Chemistry of N-Acyldihydroquinaldonitriles and N-Acyldihydroisoquinaldonitriles (Reissert Compounds)". Chemical Reviews. 55 (3): 511–549. doi:10.1021/cr50003a002. hdl:1808/32921. (Review)
  7. ^ Ahamed, Muneer; Todd, Matthew. H. (2010). "Catalytic Asymmetric Additions of Carbon-Centered Nucleophiles to Nitrogen-Containing Aromatic Heterocycles". European Journal of Organic Chemistry. 2010 (31): 5935–5942. doi:10.1002/ejoc.201000877. (Review)

Further reading

  1. Cobb, R. Lynn; McEwen, William E. (1955). "Mechanism of the Acid-catalyzed Hydrolysis of Reissert Compounds". Journal of the American Chemical Society. 77 (19): 5042. doi:10.1021/ja01624a031.
  2. McEwen, William E.; Mineo, Isidore C.; Shen, Yvonne H. (1971). "1,3-Dipolar addition reactions of Reissert compounds". Journal of the American Chemical Society. 93 (18): 4479. doi:10.1021/ja00747a023.
  3. Evanguelidou, Eleftheria K.; McEwen, William E. (1966). "Acid-Catalyzed Condensation of a Reissert Compound with Acrylonitrile". The Journal of Organic Chemistry. 31 (12): 4110. doi:10.1021/jo01350a056.
This page was last edited on 29 January 2023, at 18:34
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.