@article{02c72c4b95954792ae1f70890d40077f,
title = "Stereocontrolled synthesis of the macrolactone core of neopeltolide",
abstract = "A stereoselective synthesis of the macrolactone core of neopeltolide is described. The tetrahydropyran moiety was constructed via the intramolecular allylation of an α-acetoxy ether. A late-stage macrolactonization provided a known synthetic intermediate of neopeltolide.",
keywords = "Allylation, Convergent synthesis, Macrolide, Neopeltolide, Reductive acetylation",
author = "Andreas Meissner and Nobuhiro Tanaka and Hiroyoshi Takamura and Isao Kadota",
note = "Funding Information: This work was financially supported by JSPS KAKENHI (Grant Number 17K05863 ). Publisher Copyright: {\textcopyright} 2018 Elsevier Ltd",
year = "2019",
month = jan,
day = "31",
doi = "10.1016/j.tetlet.2018.12.066",
language = "English",
volume = "60",
pages = "432--434",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "5",
}