| Literature DB >> 29741785 |
Tomonori Misaki1, Toshifumi Tatsumi1, Tatsumasa Okamoto1, Yusuke Hayashi1, Nari Jin1, Takashi Sugimura1.
Abstract
A 1,4-addition reaction of 5H-oxazol-4-ones to alkylidene β-ketoesters, which was catalyzed by using chiral guanidines via a dynamic kinetic resolution process that involved geometric isomerization of the alkylidene β-ketoesters, was developed. This method allowed using E,Z isomeric mixture of various acyclic alkylidene β-ketoesters to obtain the products stereoselectively. The relation between the geometry and the stereoselectivity of products was investigated, and the derivatization of the products to the corresponding α-acyl-γ-lactone was performed.Entities:
Keywords: 5H-oxazol-4-ones; alkylidene β-ketoesters; asymmetric catalysis; organocatalysis; stereoconvergent reactions
Year: 2018 PMID: 29741785 DOI: 10.1002/chem.201802271
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236