The synthesis of 14C-labeled menthol was accomplished by preparation of 14C-labeled (&) pulegone. Catalytic hydrogenation and chemical reduction converted (&) pulegone to the isomeric menthols possessing 1.10 mCi total activity. Gas chromatographic separation of this material gave the relative abund
Synthesis and chiral purification of 14C-labeled novel neonicotinoids, paichongding
β Scribed by Chao Li; Xiao-Yong Xu; Ju-Ying Li; Qing-Fu Ye; Zhong Li
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- French
- Weight
- 533 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Paichongding, a novel neonicotinoids pesticide with excellent insecticidal activity against imidaclopridβresistant brown planthopper, has been sold in the Chinese market as new pesticide. [^14^C]Paichongding was proposed as a tracer to support the further study to elucidate the metabolism of the commercialized pesticide. This paper describes an efficient synthesis of [^14^C]paichongding in five radiochemical steps from [^14^C]nitromethane (1). Then the four diastereoisomers (a, b, c, and d) were separated by preparative chiral HPLC and characterized by HPLC and HPLCβLSC. This methodology could be utilized in the syntheses of other ^14^Cβlabeled nitromethylene neonicotinoids derivatives. Copyright Β© 2011 John Wiley & Sons, Ltd.
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