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An efficient Rh(II)-catalyzed denitrogenative reaction of indoles with 1,2,3-triazolyl propiolates has been developed. This methodology provides facile access to butenolide tethered homotryptamines in good to excellent yields under operationally simple… Click to show full abstract
An efficient Rh(II)-catalyzed denitrogenative reaction of indoles with 1,2,3-triazolyl propiolates has been developed. This methodology provides facile access to butenolide tethered homotryptamines in good to excellent yields under operationally simple conditions and features a broad substrate scope. Overall, the reaction sequence involves the formation of three new bonds (two C-C and one C-O) in a nucleophilic cascade manner. Additionally, an intramolecular rearrangement of these derivatives to thermodynamically more stable butenolides is also demonstrated.
Journal Title: Organic letters
Year Published: 2021
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