@article{289b5032091347679875a4abaa066d44,
title = "Synthetic studies on keramaphidin B: Formation of a macrocyclic ring by intramolecular Diels-Alder reaction",
abstract = "The possibility of constructing the macrocyclic ring of keramaphidin B via an intramolecular Diels-Alder (IMDA) reaction has been investigated. The IMDA reaction of a substrate possessing dihydropyridone and diene moieties, which were tethered by an alkyl chain including a linear triple bond, was found to proceed in the presence of SnCl4 at 80 °C.",
author = "Hiroki Shimoda and Takahiro Shibata and Daisuke Sekine and Masahisa Nakada",
note = "Funding Information: We acknowledge supports of the Materials Characterization Central Laboratory, Waseda University, for characterization of new compounds. This work was financially supported in part by JSPS KAKENHI Grant Number JP15H05841 in Middle molecular strategy and a Waseda University Grant for Special Research Projects. Publisher Copyright: {\textcopyright} 2020 The Japan Institute of Heterocyclic Chemistry.",
year = "2020",
doi = "10.3987/COM-19-14117",
language = "English",
volume = "100",
pages = "3--11",
journal = "Heterocycles",
issn = "0385-5414",
publisher = "Japan Institute of Heterocyclic Chemistry",
number = "1",
}