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Volumn 35, Issue 5, 1998, Pages 1043-1056

Development of a novel indole synthesis and its application to natural products synthesis

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Indexed keywords


EID: 0000041025     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570350504     Document Type: Article
Times cited : (73)

References (39)
  • 10
    • 85088669779 scopus 로고    scopus 로고
    • note
    • 2, 0°). Other isonitriles Ib-f were similarly prepared in 61 to 82% overall yields from o-iodoformanilide by palladium-mediated coupling reactions.
  • 11
    • 33646757152 scopus 로고    scopus 로고
    • note
    • A typical experimental procedure is as follows: A solution of an isonitrile (0.85 mmole), n-Bu3SnH (0.93 mmole), and AIBN (0.04 mmole) in 5 ml of dry acetonitrile was heated at 100° for 1 hour in a tightly capped culture tube under an argon atmosphere. The reaction mixture was partitioned between 3 W HC1 and ether. After washing the ethereal layer with a saturated KF solution, the desired indole was separated by flash silica gel chromatography.
  • 14
    • 0001688482 scopus 로고
    • The Stille coupling of l-SEM-2-tributylstannylindole with a variety of halides has recently been reported: G. Palmisano and M. Santagostino, Helv. Chim. Acta, 76, 2356 (1993).
    • (1993) Helv. Chim. Acta , vol.76 , pp. 2356
    • Palmisano, G.1    Santagostino, M.2
  • 29
    • 0016301365 scopus 로고
    • A. I. Scott, Bioorg. Chem., 3, 398 (1974) and references cited therein.
    • (1974) Bioorg. Chem. , vol.3 , pp. 398
    • Scott, A.I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.