Fries rearrangement (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fries rearrangement" in English language version.

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Fries, K.; Finck, G. (1908). "Über Homologe des Cumaranons und ihre Abkömmlinge". Chemische Berichte. 41 (3): 4271–4284. doi:10.1002/cber.190804103146.
Fries, K.; Pfaffendorf, W. (1910). "Über ein Kondensationsprodukt des Cumaranons und seine Umwandlung in Oxindirubin". Chemische Berichte. 43 (1): 212–219. doi:10.1002/cber.19100430131.
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "photo-Fries rearrangement". doi:10.1351/goldbook.P04614
Belluš, Daniel (5 January 2007). "Photo-Fries Rearrangement and Related Photochemical [1,j] -Shifts (j = 3, 5, 7) of Carbonyl and Sulfonyl Groups". Advances in Photochemistry. 8: 109–159. doi:10.1002/9780470133385.ch3. ISBN 9780470133385.
Searle, Norma D. (7 November 2004). "Environmental Effects on Polymeric Materials". Plastics and the Environment. 8: 311–358. doi:10.1002/0471721557.ch8. ISBN 9780471721550.
Korb, Marcus; Lang, Heinrich (2019). "The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics". Chemical Society Reviews. 48 (10): 2829–2882. doi:10.1039/C8CS00830B. PMID 31066387. S2CID 206131063.

Korb, Marcus; Lang, Heinrich (2019). "The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics". Chemical Society Reviews. 48 (10): 2829–2882. doi:10.1039/C8CS00830B. PMID 31066387. S2CID 206131063.

Korb, Marcus; Lang, Heinrich (2019). "The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics". Chemical Society Reviews. 48 (10): 2829–2882. doi:10.1039/C8CS00830B. PMID 31066387. S2CID 206131063.