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Volumn , Issue 11, 2002, Pages 1904-1906

Stille reaction on pyridinium cations

Author keywords

Heteroaromatic cations; Molecular electronic devices; Stille reaction

Indexed keywords

PYRIDINIUM DERIVATIVE; TIN DERIVATIVE;

EID: 0036425891     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-34903     Document Type: Article
Times cited : (18)

References (36)
  • 16
    • 0001186913 scopus 로고
    • Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, Chap. 3.4
    • (b) Farina, F. Comprehensive Organometallic Chemistry II, Vol. 12; Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, 1995, Chap. 3.4, 161.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 161
    • Farina, F.1
  • 24
  • 30
    • 0011277173 scopus 로고    scopus 로고
    • note
    • 4 (0.0165 mmol, 15.1 mg). The reaction mixture was heated at 80°C or stirred at r.t. (as indicated) and then filtered through a small pad of celite and washed with methanol. The solvent was removed and the residue was triturated with EtOAc. Purification of the crude product by column chromatography on silica gel (reverse phase), using water as the eluent yielded the coupling product.
  • 32
    • 0011319635 scopus 로고    scopus 로고
    • note
    • 3 (0.0165 mmol, 5 mg) were slowly added followed by the corresponding stannane (1.3 equiv, 0.429 mmol). The mixture was stirred at r.t. and the work-up procedure, which was similar to Method A, yielded the coupling product.
  • 35
    • 0011277174 scopus 로고    scopus 로고
    • note
    • 3 (0.0165 mmol, 5 mg) and 1.3 equiv KF (0.429 mmol, 24.9 mg) were slowly added followed by 1.3 equiv of the corresponding stannane (0.429 mmol). The reaction mixture was heated at 80°C (as indicated), the residue was triturated with acetonitrile and the liquid was purified by column chromatography on silica gel (reverse phase) using water as the eluent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.