Well-known reactions and reagents in organic chemistry include

0-9

A

B

C

D

E

F

G

H

I

J

K

L

M

N

O

P

Q

R

S

T

U

V

W

Y

Z

See also

Wikimedia Commons has media related to Organic reactions.

References

  1. ↑ Treibs, Wilhelm; Schmidt, Harry (1927). "Zur katalytischen Dehydrierung hydro-aromatischer Verbindungen" [Catalytic dehydrogenation of hydroaromatic compounds]. Berichte der Deutschen Chemischen Gesellschaft (in German). 60 (10): 2335–2341. doi:10.1002/cber.187600901134.
  2. ↑ Alder, Kurt; Nobel, Theo (1943). "Über die Anlagerung von Azodicarbonsäure-ester an Aldehyde" [Substituting additions. II. Addition of azodicarboxylic esters to aldehydes.]. Berichte der Deutschen Chemischen Gesellschaft (in German). 76 (1): 54–57. doi:10.1002/cber.19430760106.
  3. ↑ Alder, Kurt; Pascher, Franz; Schmitz, Andreas (1943). "Über die Anlagerung von Maleinsäure-anhydrid und Azodicarbonsäure-ester an einfach ungesättigte Koh an einfach ungesättigte Kohlenwasserstoffe. Zur Kenntnis von Substitutionsvorgängen in der Allyl-Stellung" [Substituting additions. I. Addition of maleic anhydride and azodicarboxylic esters to singly unsaturated hydrocarbons. Substitution processes in the allyl position]. Berichte der Deutschen Chemischen Gesellschaft. 76 (1): 27–53. doi:10.1002/cber.19430760105.
  4. ↑ Alder, Kurt; Schmidt, Carl-Heinz (1943). "Über die Kondensation des Furans und seiner Homologen mit α,β-ungesättigten Ketonen und Aldehyden†Aufbau von Di-, Tri- und Tetraketonen der Fettreihe" [Substituting additions. III. Condensation of furan and its homologs with α,β-unsaturated ketones and aldehydes. Synthesis of di-, tri-and tetraketones of the aliphatic series.]. Berichte der Deutschen Chemischen Gesellschaft (in German). 76 (3): 183–205. doi:10.1002/cber.19430760302.
  5. ↑ Aston, J. G.; Greenburg, R. B. (1942). "alpha-Bromo Secondary Alkyl Ketones. I. Reaction with Sodium Alcoholates. A New Synthesis of Tertiary Acids by Rearrangement1,2". Journal of the American Chemical Society. 62 (10): 2590–2595. doi:10.1021/ja01867a003.
  6. ↑ Wang, Zerong (2010). Comprehensive Organic Name Reactions and Reagents. doi:10.1002/9780470638859.conrr026. ISBN 9780471704508.
  7. ↑ Sacks, Abraham A.; Aston, J. G. (1951). "α-Halo Ketones. V. The Preparation, Metathesis and Rearrangement of Certain α-Bromoketones". Journal of the American Chemical Society. 73 (8): 3902–3906. doi:10.1021/ja01152a103.
  8. ↑ Wagner, R. B.; Moore, James A. (1950). "The Reaction of the Isomeric α-Bromomethyl Cyclohexyl Ketones with Sodium Methoxide". Journal of the American Chemical Society. 72 (7): 2884–2887. doi:10.1021/ja01163a022.
  9. ↑ Oehlschlager, A. C.; Zalkow, L. H. (1965). "Bridged Ring Compounds. X.1,2 The Reaction of Benzenesulfonyl Azide with Norbornadiene, Dicyclopentadiene, and Bicyclo[2.2.2]-2-octene". The Journal of Organic Chemistry. 30 (12): 4205–4211. doi:10.1021/jo01023a051.
  10. ↑ Hill, Richard K.; Gilman, Norman W. (1967). "A nitrogen analog of the Claisen rearrangement". Tetrahedron Letters. 8 (15): 1421–1423. doi:10.1016/S0040-4039(00)71596-6.
  11. ↑ Lipkowitz, K. B.; Scarpone, S.; McCullough, D.; Barney, C. (1979). "The synthesis of N-substituted tetrahydropyridines using the hetero-cope rearrangement". Tetrahedron Letters. 20 (24): 2241–2244. doi:10.1016/S0040-4039(01)93686-X.
  12. ↑ Baeyer, Adolf; Villiger, Victor (1899). "Einwirkung des Caro'schen Reagens auf Ketone" [The effect of Caro's reagent on ketones]. Berichte der Deutschen Chemischen Gesellschaft (in German). 32 (3): 3625–3633. doi:10.1002/cber.189903203151.
  13. ↑ Baker, Wilson (1933). "Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones". Journal of the Chemical Society: 1381–1389. doi:10.1039/JR9330001381.
  14. ↑ Baker, Wilson (1934). "Attempts to synthesise 5,6-dihydroxyflavone (primetin)". Journal of the Chemical Society: 1953–1954. doi:10.1039/JR9340001953.
  15. ↑ Mahal, Harbhajan S.; Venkataraman, Krishnasami (1934). "Synthetical experiments in the chromone group. Part XIV. The action of sodamide on 1-acyloxy-2-acetonaphthones". Journal of the Chemical Society: 1767–1769. doi:10.1039/JR9340001767.
  16. ↑ Bhalla, Diwan C.; Mahal, Harbhajan S.; Venkataraman, Krishnasami (1935). "Synthetical experiments in the chromone group. Part XVII. Further observations on the action of sodamide on o-acyloxyacetophenones". Journal of the Chemical Society: 868–870. doi:10.1039/JR9350000868.
  17. ↑ Baldwin, Jack E. (1976). "Rules for ring closure". Journal of the Chemical Society, Chemical Communications (18): 734–736. doi:10.1039/C39760000734.
  18. 1 2 Balz, Günther; Schiemann, Günther (1927). "Über aromatische Fluorverbindungen, I.: Ein neues Verfahren zu ihrer Darstellung" [Aromatic fluorine compounds. I. A new method for their preparation]. Berichte der Deutschen Chemischen Gesellschaft (in German). 60 (5): 1186–1190. doi:10.1002/cber.19270600539.
  19. ↑ Bartoli, Giuseppe; Leardini, Rino; Medici, Alessandro; Rosini, Goffredo (1978). "Reactions of nitroarenes with Grignard reagents. General method of synthesis of alkyl-nitroso-substituted bicyclic aromatic systems". Journal of the Chemical Society, Perkin Transactions 1 (7): 692–696. doi:10.1039/P19780000692.
  20. ↑ Bartoli, Giuseppe; Palmieri, Gianni; Bosco, Marcella; Dalpozzo, Renato (1989). "The reaction of vinyl grignard reagents with 2-substituted nitroarenes: A new approach to the synthesis of 7-substituted indoles". Tetrahedron Letters. 30 (16): 2129–2132. doi:10.1016/S0040-4039(01)93730-X.
  21. ↑ Bartoli, Giuseppe; Bosco, Marcella; Dalpozzo, Renato; Palmieri, Gianni; Marcantoni, Enrico (1991). "Reactivity of nitro- and nitroso-arenes with vinyl grignard reagents: synthesis of 2-(trimethylsilyl)indoles". Journal of the Chemical Society, Perkin Transactions 1 (11): 2757–2761. doi:10.1039/P19910002757.
  22. ↑ Barton, D. H. R.; Beaton, J. M.; Geller, L. E.; Pechet, M. M. (1960). "A new photochemical reaction". Journal of the American Chemical Society. 82 (10): 2640–2641. doi:10.1021/ja01495a061.
  23. ↑ Barton, D. H. R.; Beaton, J. M.; Geller, L. E.; Pechet, M. M. (1961). "A new photochemical reaction". Journal of the American Chemical Society. 83 (19): 4076–4083. doi:10.1021/ja01480a030.
  24. ↑ Cope, Arthur C.; Hardy, Elizabeth M. (1940). "The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System". Journal of the American Chemical Society. 62 (2): 441–444. doi:10.1021/ja01859a055.
  25. ↑ Finkelstein, Hans (1910). "Darstellung organischer Jodide aus den entsprechenden Bromiden und Chloriden" [Preparation of Organic Iodides from the Corresponding Bromides and Chlorides]. Berichte der Deutschen Chemischen Gesellschaft (in German). 43 (2): 1528–1532. doi:10.1002/cber.19100430257.
  26. ↑ Corey, E. J.; Chaykovsky, Michael (1962). "Dimethylsulfoxonium Methylide". Journal of the American Chemical Society. 84 (5): 867–868. doi:10.1021/ja00864a040.
  27. ↑ Corey, E. J.; Chaykovsky, Michael (1965). "Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic Synthesis". Journal of the American Chemical Society. 87 (6): 1353–1364. doi:10.1021/ja01084a034.
  28. ↑ Bowden, K.; Heilbron, I. M.; Jones, E. R. H.; Weedon, B. C. L. (1946). "Researches on acetylenic compounds. Part I. The preparation of acetylenic ketones by oxidation of acetylenic carbinols and glycols". Journal of the Chemical Society: 39–45. doi:10.1039/JR9460000039.
  29. ↑ Bowers, A.; Halsall, T. G.; Jones, E. R. H.; Lemin, A. J. (1953). "The chemistry of the triterpenes and related compounds. Part XVIII. Elucidation of the structure of polyporenic acid C". Journal of the Chemical Society: 2548–2560. doi:10.1039/JR9530002548.
  30. ↑ Julia, Marc; Paris, Jean-Marc (1973). "Syntheses a l'aide de sulfones v(+)- methode de synthese generale de doubles liaisons" [Syntheses with the help of sulfones. V. General method of synthesis of double bonds]. Tetrahedron Letters (in French). 14 (49): 4833–4836. doi:10.1016/S0040-4039(01)87348-2.
  31. ↑ Reformatsky, Sergius (1887). "Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen". Berichte der Deutschen Chemischen Gesellschaft. 20 (1): 1210–1211. doi:10.1002/cber.188702001268.
  32. ↑ Ritter, John J.; Kalish, Joseph (1948). "A New Reaction of Nitriles. II. Synthesis of t-Carbinamines". Journal of the American Chemical Society. 70 (12): 4048–4050. doi:10.1021/ja01192a023. PMID 18105933.
  33. ↑ Ritter, John J.; Minieri, P. Paul (1948). "A New Reaction of Nitriles. I. Amides from Alkenes and Mononitriles". Journal of the American Chemical Society. 70 (12): 4045–4048. doi:10.1021/ja01192a022. PMID 18105932.
  34. ↑ Katsuki, Tsutomu; Sharpless, K. Barry (1980). "The first practical method for asymmetric epoxidation". Journal of the American Chemical Society. 102 (18): 5974–5976. doi:10.1021/ja00538a077.

Organic Chemistry at Curlie

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.