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Article Abstract
A one-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction has been explored for the first time, facilitating the synthesis of the unprecedented 2,3-disubstituted-5-quaternary-4-amidocyclopent-2-enone and 2-quaternary-3-amidoindanones. This transformation features convenient operation, good yields (up to 70%), and good to excellent diastereoselectivity (up to 20 : 1). The proposed reaction mechanism is supported by some experimental results.
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| http://dx.doi.org/10.1039/d4cc06597b | DOI Listing |
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