## Abstract A simple strategy for the small‐scale synthesis of the ^15^__N__‐labelled insecticide phosmet has been developed, starting from ^15^__N__‐phthalimide‐K. Copyright © 2004 John Wiley & Sons, Ltd.
Synthesis of the 15N-labelled insecticide imidacloprid
✍ Scribed by Nicole Schippers; Wolfgang Schwack
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 97 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A five‐step synthesis of the neonicotinoid insecticide imidacloprid (1) labelled with ^15^N is reported in an overall yield of 10%. The stable isotope ^15^N was introduced in the pyridine part by reaction of ^15^NH~3~ with coumalic acid methyl ester (2) to ^15^N‐hydroxy nicotinic acid (3) followed by further reactions to ^15^N‐2‐chloro‐5‐(chloromethyl) pyridine (6) which was coupled with N‐nitroimidazolidin‐2‐imine to yield 1. Copyright © 2006 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
Imidacloprid analogues containing a nitroalkylidene instead of a nitroguanidine unit have been prepared and evaluated for investigation as potential insecticides. No nitroalkylidene analogue showed signiÐcant activity against the test insects.
## Abstract The synthesis of ^15^N‐labelled nornicotine **2** and ^15^N‐labelled nicotine **1** is described via the reductive aminocyclization of a 1,4‐ketoaldehyde with a corresponding amine in the presence of sodium cyanoborohydride. Yields of 30% and 26%, respectively, were obtained from 3‐brom
## Abstract The ifosfamide metabolite isophosphoramide mustard (IPM) was synthesized with isotopic enrichment at each nitrogen site. Glycine‐^15^__N__ was converted to 2‐chloroethylamine‐^15^__N__ hydrochloride (4 steps, 21% net yield) which was then reacted with phenyl dichlorophosphate to provide
The synthesis of 15N labelled nylon 6 by anionic polymerization of Ecaprolactam is described. Labelling of this commercially important polymer should greatly enhance investigations of its morphology by techniques such as NMR, IR, and Raman spectroscopies.
A new technique was developed for the large-scale synthesis of lSN-labelled urea at low enrichment levels. The synthesis is based on nucleophilic displacement of the phenoxide ion from phenyl carbonate and uses anhydrouli Pmmonia as the nucleophile. In previous reports a copper catalyst was used; ho