An efficient synthesis of pregaliellalactone and desoxygaliellalactone

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Bibtex

@article{2355bb4cc2474cf4acba980a59ec72b3,
title = "An efficient synthesis of pregaliellalactone and desoxygaliellalactone",
abstract = "A short and efficient total synthesis of rac-desoxygaliellalactone and (+)-desoxygaliellalactone, via the biosynthetic intermediate pregaliellalactone, is described. The synthesis was achieved in only three steps, for (+)-desoxygaliellalactone including an enantioselective alkyl propiolate addition to 4-pentenal, a palladium catalysed alkylative lactonisation and an intramolecular Diels-Alder cycloaddition. (C) 2014 Elsevier Ltd. All rights reserved.",
keywords = "Natural product, Pregaliellalactone, Desoxygaliellalactone, Galiellalactone, Enantioselective, Biosynthesis",
author = "Furuseth, {Eira Ruud} and Rikard Larsson and Narda Blanco and Johansson, {Martin H} and Olov Sterner",
year = "2014",
doi = "10.1016/j.tetlet.2014.04.117",
language = "English",
volume = "55",
pages = "3667--3669",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "27",

}