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Volumn , Issue 19, 1999, Pages 2669-2670

Convenient synthesis of methyl iridol-2-y-IpropioIate

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Indexed keywords


EID: 0001154411     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a906023e     Document Type: Article
Times cited : (25)

References (28)
  • 15
    • 33746519612 scopus 로고    scopus 로고
    • 5c was prepared by lithiumzinc transmetallation of the corresponding lithium derivative generated in THF at -78 °C with BuLi.
    • The required zinc chloride derivative 5c was prepared by lithiumzinc transmetallation of the corresponding lithium derivative generated in THF at -78 °C with BuLi.
    • Zinc Chloride Derivative
    • Required, T.1
  • 18
    • 33746532740 scopus 로고    scopus 로고
    • note
    • 1H-NMR (CDC13) 0 8.25 (1H, d), 7.95 (2H, AA' part of AA'BB' system), 7.50 (1H, d), 7.45 (1H, t), 7.25 (1H, t), 7.15 (1H, s), 6.90 (2H, BB' part of AA'BB' system), 3.90 (3H, s), 3.80 (3H, s). C-NMR (CDC1,)5 164.5, 163.1, 138.5, 135.1 (2C), 134.2, 132.1, 129.9, 127.8, 127.0, 124.1, 121.8, 114.7, 114.5 (2C), 76.6, 68.5, 55.7, 52.9; Anal. Calcd for CH15NO5S: C 61.78, H 4.10, N 3.79. Found: C 61.83, H 4.22, N 3.87%.
  • 23
    • 33746522544 scopus 로고    scopus 로고
    • 1995, 27, 129. The Sonogashira reaction has been applied also to the synthesis of indol-2-yl-acetylenes: see réf. 2(b),(e).
    • R. Rossi, A. Carpita and F. Bellina, Org. Prep. Proced. Int., 1995, 27, 129. The Sonogashira reaction has been applied also to the synthesis of indol-2-yl-acetylenes: see réf. 2(b),(e).
    • A. Carpita and F. Bellina, Org. Prep. Proced. Int.
    • Rossi, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.