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Article

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Accepted version

Publication date

2011-04

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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/172794

Enantioselective Syntehsis of Alkaloids from Phenylglycinol-derived lactams

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https://doi.org/10.1039/b400987h

Abstract

This review is focused on recent synthetic achievements and ongoing work in our laboratory using phenylglycinol-derived oxazolopiperidone lactams as starting materials for the enantioselective synthesis of piperidine-containing alkaloids: madangamines, 2,5-disubstituted decahydroquinoline and 1-substituted tetrahydroisoquinoline alkaloids, the indole alkaloids 20S- and 20R-dihydrocleavamine and quebrachamine, and indole alkaloids of the uleine and silicine groups. Keywords: alkaloids, piperidine, indole, lactams, total synthesis, phenylglycinol.

Subject

Alcaloides, Lactames, Síntesi orgànica

Subject (English)

Alkaloids, Lactams, Organic synthesis

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Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)

Citation

AMAT TUSÓN, Mercedes, et al. Enantioselective Syntehsis of Alkaloids from Phenylglycinol-derived lactams. Natural Product Communications. 2011. Vol. 6, num. 4, pags. 515-526. ISSN 1934-578X. [consulted: 12 of June of 2026]. Available at: https://hdl.handle.net/2445/172794

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