| Literature DB >> 35719215 |
Amber M Kelley1, Joshua A Frost1, Tylisha M Baber1, Kala C Youngblood1, Emiri Michishita1, Schuyler A Bain1, T Caleb Lykins1, Kimberly S Petersen1.
Abstract
Nitriles are important organic functional groups, allowing for installation of nitrogen in organic synthesis. The Pinner reaction transforms nitriles into esters via the imidate group, but in general has previously necessitated harsh acid conditions. This work builds on the utility of the Pinner reaction through a stereoselective desymmetrization of dinitriles to form γ- and δ-lactones in good yields and diastereoselectivites.Entities:
Keywords: Desymmetrization; Diastereoselective; Lactones; Pinner Reaction
Year: 2021 PMID: 35719215 PMCID: PMC9205472 DOI: 10.1016/j.tetlet.2021.153573
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.032