A general strategy for the synthesis of indolyl cyclopropanecarbaldehydes and ketones via a Brønsted acid-catalyzed indole nucleophilic addition/ring-contraction reaction sequence has been exploited. The procedure leads to a wide panel of cyclopropyl carbonyl compounds in generally high yields with a broad substrate scope.
Catalytic Tandem Friedel–Crafts Alkylation/C4–C3 Ring-Contraction Reaction: An Efficient Route for the Synthesis of Indolyl Cyclopropanecarbaldehydes and Ketones
Alberto LuridianaSecondo
Membro del Collaboration Group
;COCCO, ANDREAMembro del Collaboration Group
;Stefania PorcuMembro del Collaboration Group
;Angelo FrongiaMembro del Collaboration Group
;Giorgia SaraisPenultimo
Membro del Collaboration Group
;Francesco Secci
Ultimo
Membro del Collaboration Group
2019-01-01
Abstract
A general strategy for the synthesis of indolyl cyclopropanecarbaldehydes and ketones via a Brønsted acid-catalyzed indole nucleophilic addition/ring-contraction reaction sequence has been exploited. The procedure leads to a wide panel of cyclopropyl carbonyl compounds in generally high yields with a broad substrate scope.File in questo prodotto:
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