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- W2241202058 abstract "A new approach to secoiridoids, based on the synthesis of the key functionalized intermediates 4 and 5, is presented. These compounds were tested in formal [3+3] cycloadditions. Acyl-chloride 15 was transformed into enol α,β-unsaturated ester 16, which was involved in a N-heterocyclic carbene rearrangement to give an advanced precursor 17 in the total synthesis of secoiridoids." @default.
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- W2241202058 date "2015-10-01" @default.
- W2241202058 modified "2023-10-16" @default.
- W2241202058 title "Studies towards the synthesis of secoiridoids" @default.
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- W2241202058 doi "https://doi.org/10.1016/j.tet.2015.07.067" @default.
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