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Novel method for the synthesis of α-bromocinnamaldehydes

✍ Scribed by A. V. Shastin; A. L. Reznichenko; O. N. Lenkova; E. S. Balenkova; V. G. Nenaidenko

Publisher
Springer
Year
2005
Tongue
English
Weight
235 KB
Volume
54
Category
Article
ISSN
1573-9171

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The conventional method for the synthesis of a-fluoroketones was the action of per&oryl fluoride on ketone enamines. Though this reagent has been successful, mainly with steroidal ketones,') it has well-known and serious limitations. Thus the reagent can beueed only with very electron-rich olefins.