Methylene Group Modifications of the N-(Isothiazol-5-yl)phenylacetamides. Synthesis and Insecticidal Activity
Author:
Affiliation:
1. Discovery Research, Dow AgroSciences, 9330 Zionsville Road, Indianapolis, Indiana 46268-1054
Publisher
American Chemical Society (ACS)
Subject
General Agricultural and Biological Sciences,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jf990095s
Reference13 articles.
1. Abraham, R. J.; Loftus, P.Proton and Carbon-13 NMR Spectroscopy; Heyden: London, 1978; pp 23−24.
2. A new route to α-hetero β-enamino esters using a mild and convenient solvent-free process assisted by focused microwave irradiation
3. Hackler, R. E.; Johnson, G. W.; Samaritoni, J. G.N-(5-Isothiazolyl)amide Pesticides. WO 95/31448, 1995.
4. Enamine oxidations. 2. Selective oxidative cleavage of β,β - disubstituted enamines using alumina supported permanganate. Synthesis of one-carbon dehomologated carbonyl compounds from enamines
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