Journal ArticleOPEN ACCESS

Synthetic studies on keramaphidin B: Formation of a macrocyclic ring by intramolecular Diels-Alder reaction

Heterocycles (2020) 100(1) 3-11
DOI: 10.3987/COM-19-14117
5Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Shimoda, H., Shibata, T., Sekine, D., & Nakada, M. (2020). Synthetic studies on keramaphidin B: Formation of a macrocyclic ring by intramolecular Diels-Alder reaction. Heterocycles, 100(1), 3–11. https://doi.org/10.3987/COM-19-14117

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free