Abstract
As highlighted in this mini-review, a growing area of interest in organic synthesis involves the use of substituted carbonyl ylides as 1,3-dipoles for the preparation of alkaloidal natural products. Cascade reactions proceeding by an intramolecular 1,3-dipolar cycloaddition of carbonyl ylides are of particular interest to the synthetic organic community because of the increase in molecular complexity involved and the high isolated yields.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2183—2194, September, 2016.
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Padwa, A. Cycloaddition chemistry of carbonyl ylides for alkaloid synthesis. Russ Chem Bull 65, 2183–2194 (2016). https://doi.org/10.1007/s11172-016-1566-x
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DOI: https://doi.org/10.1007/s11172-016-1566-x