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玉嘧磺隆的合成 被引量:3

Synthesis of Rimsulfuron
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摘要 对合成玉嘧磺隆文献进行了综述,提出了合理的合成路线,并运用固体光气合成玉嘧磺隆,产品纯度大于96%(HPLC法),总收率不小于36%。所有中间体及目标化合物的结构用1HNMR、IR及MS进行了表征。 The reasonable synthesis method of rimsulfuron was given based on summarization of literatures published. The intermediates were prepared and the title compound was synthesized by triphosgene at last. The purity of the product was over 96%(by HPLC), and the total yield was not less than 36%. The structures of all compounds synthesized were determined by ^1HNMR, IR and MS.
出处 《农药》 CAS 北大核心 2005年第12期541-543,共3页 Agrochemicals
基金 2005年江苏省科技攻关(三药)项目(BE2005611)
关键词 玉嘧磺隆 磺酰脲除草剂 吡啶类化合物 固体光气 rimsulfuron, sulfonylurea herbicides, pyridine derivatives, triphosgene
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参考文献6

  • 1George L, Wilmington D. Agricultural pyridinesulfonamides[P]. US 4435206, 1984.
  • 2Shapiro R. Herbicidal sulfonamides[P]. EP 0084224, 1982.
  • 3Bryson T A, Donelson D M, Dunlap B, et al. Biological probes.3.Methods for carbon-4 and carbon-5 labeling in nicotinamide[J]. J Org Chem, 1976, 41(11): 2065-2067.
  • 4Bryson T A, Wisowaty R B, Dunlap B, et al. Biological probes.Ⅱ.Ring labeled nicotin-amide[J]. J Org Chem, 1974, 39(23):3436-3438.
  • 5Chlang, Chlh-Shu G. Cyano-dienes,halopyridines and a process for their preparation[P]. EP 0323881, 1989.
  • 6chr(O)der, Ludwig. Preparation of 2-chloropyridine derivatives[P]. EP 0462639, 1991.

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