Radical cyclization of allyl α-bromocarboxylates into γ-butyrolactones. Effect of the ester structure on the cyclization

DOI: 10.1007/BF02495259

Source and publish data:

Russian Chemical Bulletin p. 2096 - 2098 (1997)

Update date:2022-08-04

Topics:

Authors:

Terent'ev

Vasil'eva

Kuz'mina

Ikonnikov

Orlova Orlova

Mysov Mysov

Belokon'

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Article abstract of DOI:10.1007/BF02495259

Allyl dibromoacetate, allyl α-bromopropionate, and allyl phenylbromoacetate undergo cyclization in benzene in the presence of increased concentration of Fe(CO)₅ - DMF as the initiating system to give the corresponding bromo-substituted butyrolactones.

Full text of DOI:10.1007/BF02495259

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