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Volumn 40, Issue 3-4, 2000, Pages 301-306

Design and preparation of polyphenyl distance markers for solid-state 19F NMR

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EID: 0034561227     PISSN: 00212148     EISSN: None     Source Type: Journal    
DOI: 10.1560/9T7N-K3L6-TTUF-359R     Document Type: Article
Times cited : (5)

References (21)
  • 12
    • 0039596111 scopus 로고    scopus 로고
    • The quarterphenyl compound, 4-trifluoromethyl-4‴-trifluoromethylthio-p-quaterphenyl was prepared following the same sequential coupling, but the yield was low due to low solubility in solvents. Solid-state NMR measurements have not been successful with this compound
    • The quarterphenyl compound, 4-trifluoromethyl-4‴-trifluoromethylthio-p-quaterphenyl was prepared following the same sequential coupling, but the yield was low due to low solubility in solvents. Solid-state NMR measurements have not been successful with this compound.
  • 14
    • 84943950090 scopus 로고
    • and references cited therein
    • (b) Suzuki, A.; Miyaura, N. Pure Appl. Chem. 1991, 63, 419-422 and references cited therein.
    • (1991) Pure Appl. Chem. , vol.63 , pp. 419-422
    • Suzuki, A.1    Miyaura, N.2
  • 18
    • 0040187369 scopus 로고    scopus 로고
    • Due to the unsuccessful synthesis of 4-methyl-4″-methylthio-p-terphenyl, mimic compound 6 was used as the dilutant
    • Due to the unsuccessful synthesis of 4-methyl-4″-methylthio-p-terphenyl, mimic compound 6 was used as the dilutant.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.