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Russian Chemical Reviews, 1970, Volume 39, Issue 9, Pages 732–746
DOI: https://doi.org/10.1070/RC1970v039n09ABEH002019
(Mi rcr2387)
 

This article is cited in 67 scientific papers (total in 67 papers)

The Favorskii Rearrangement

A. A. Akhrem, T. K. Ustynyuk, Yu. A. Titov

N. D. Zelinskii Institute of Organic Chemistry of the USSR Academy of Sciences, Moscow
English full-text Citations (67)
Abstract: The skeletal rearrangement of α-halogeno-ketones, which is known as the Favorskii rearrangement, is met most frequently in aliphatic monocyclic, and polycyclic halogenated ketones. This molecular rearrangement is used in the synthesis of branched carboxylic acids and cis-αβ-unsaturated acids and for obtaining smaller rings in alicyclic and to a less extent heterocyclic compounds. The sterochemistry and the mechanism of the Favorskii rearrangement are also considered, these being of great interest for theoretical organic chemistry. A list of 261 references is included.
Russian version:
Uspekhi Khimii, 1970, Volume 39, Issue 9, Pages 1560–1590
DOI: https://doi.org/10.1070/RC1970v039n09ABEH002019
Bibliographic databases:
Document Type: Article
UDC: 547.314
Language: English
Original paper language: Russian


Citation: A. A. Akhrem, T. K. Ustynyuk, Yu. A. Titov, “The Favorskii Rearrangement”, Usp. Khim., 39:9 (1970), 1560–1590; Russian Chem. Reviews, 39:9 (1970), 732–746
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