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Volumn 73, Issue 21, 2008, Pages 8545-8552

Synthesis of new fluorinated tebufenpyrad analogs with acaricidal activity through regioselective pyrazole formation

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Indexed keywords

CHEMICAL REACTIONS;

EID: 55249098392     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801729p     Document Type: Article
Times cited : (127)

References (19)
  • 16
    • 55249085929 scopus 로고    scopus 로고
    • 2), which were obtained by amidation of the corresponding carboxylic acids 17 and 21, respectively. Under the same reaction conditions described above, chlorination of 30′ and 32′ afforded complex mixtures of products. Likewise, the desired results were not obtained when other chlorination agents such as NCS, Chloramine-T, and tert-butyl hypochlorite were used in the reaction with the carboxylic acids 17-21.
    • 2), which were obtained by amidation of the corresponding carboxylic acids 17 and 21, respectively. Under the same reaction conditions described above, chlorination of 30′ and 32′ afforded complex mixtures of products. Likewise, the desired results were not obtained when other chlorination agents such as NCS, Chloramine-T, and tert-butyl hypochlorite were used in the reaction with the carboxylic acids 17-21.
  • 18
    • 55249124842 scopus 로고    scopus 로고
    • Masai is commercialized by BASF
    • Masai is commercialized by BASF.
  • 19
    • 55249111153 scopus 로고    scopus 로고
    • The concentration of Tebufenpyrad in solution for standard field treatment varies between 200 mg/L (pumpkin, eggplant, tomato), 130 mg/L (cotton), and 70 mg/L (citrus fruits).
    • The concentration of Tebufenpyrad in solution for standard field treatment varies between 200 mg/L (pumpkin, eggplant, tomato), 130 mg/L (cotton), and 70 mg/L (citrus fruits).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.