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Volumn 46, Issue 44, 2005, Pages 7549-7552

A convenient synthesis of (E)-α-alkylidene-γ-lactams and (E)-3-alkylideneoxindoles by rhodium-catalyzed intramolecular hydroamidation

Author keywords

C H activation; Carbonylative cyclization; Formamides; Hydroamidation; Rhodium catalyst

Indexed keywords

FORMAMIDE; GAMMA LACTAM DERIVATIVE; INDOLE DERIVATIVE; RHODIUM;

EID: 26244459185     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.08.133     Document Type: Article
Times cited : (39)

References (40)
  • 20
    • 2942557280 scopus 로고    scopus 로고
    • For a recent review, see: I. Nakamura, and Y. Yamamoto Chem. Rev. 104 2004 2127 and references cited therein
    • (2004) Chem. Rev. , vol.104 , pp. 2127
    • Nakamura, I.1    Yamamoto, Y.2
  • 29
    • 0035812792 scopus 로고    scopus 로고
    • For recent examples of (Z)-α-alkylidene-γ-lactams, see: X. Xie, X. Lu, Y. Liu, and W. Xu J. Org. Chem. 66 2001 6545
    • (2001) J. Org. Chem. , vol.66 , pp. 6545
    • Xie, X.1    Lu, X.2    Liu, Y.3    Xu, W.4
  • 35
    • 26244437307 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra.
  • 36
    • 26244465497 scopus 로고    scopus 로고
    • note
    • 12 (0.020 mmol), and xylene (1.0 mL) was placed in a Pyrex flask with a magnetic stirring bar under an argon atmosphere. The mixture was then magnetically stirred at 130°C (oil bath temp.) for 5-10 h. After cooling to room temperature, column chromatograph on silica gel (eluent: hexane/EtOAc = 10:1-5:1) gave the products 2a-g.
  • 38
    • 26244442289 scopus 로고    scopus 로고
    • note
    • 7c.
  • 40
    • 26244437502 scopus 로고    scopus 로고
    • note
    • Further application of this method to the synthesis of β- and δ-lactams will be reported in the near future.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.