Novel exocyclic enamides: synthesis and evaluation of the fungicidal activities of 5-methylene-2-(trifluoromethyl)morpholin-3-one derivatives. Issue 122 (23rd November 2015)

• Record Type: Journal Article
• Authors: Tian, Lei; Cui, Can; Zhu, Cong; Yang, Hui-Hui; Li, Jian-Qiang; Zhao, Wei-Guang
• Is Part Of: RSC advances. Volume 5:Issue 122(2015)
• Page Start: 100418
• Page End: 100423
• Publication Date: 2015-11-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra20138a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A facile and efficient protocol has been developed for the synthesis of a series of new 5-methylenemorpholin-3-one derivatives, which are exocyclic enamides. Some of them exhibited very good in vitro fungicidal activity against P. oryzae . Abstract : Exocyclic enamides have been used extensively in the synthesis of natural products and biologically active substances. A facile and efficient protocol has been developed for the synthesis of a series of new 5-methylenemorpholin-3-one derivatives, which are exocyclic enamides, based on the reactions of trifluoroatrolactamides with propargyl bromide in the presence of sodium hydride. The biological evaluation of these compounds showed that some of them exhibited very good in vitro fungicidal activity against P. oryzae . For example, compounds2d and2e gave fungicidal activities of 50% at a concentration of 0.9 μg mL −1, whilst the control compound fenaminstrobin gave 80% activity at the same concentration.