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Volumn , Issue 2, 2000, Pages 227-229

Reactions of trimethylstannyl ions with mono-, di- and trichloro- substituted aromatic substrates by the S(RN)1 mechanism

Author keywords

Bis(trimethylstannyl)benzenes; Bis(trimethylstannyl)pyridines; Photostimulation; S(RN)1 reactions; Tin nucleophiles

Indexed keywords

1,2 DICHLOROBENZENE; 1,3,5 TRICHLOROBENZENE; AMMONIA; AROMATIC COMPOUND; BENZENE DERIVATIVE; CHLOROBENZOIC ACID DERIVATIVE; NITRILE; PYRIDINE DERIVATIVE; SODIUM; TIN DERIVATIVE;

EID: 0038286828     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-6502     Document Type: Article
Times cited : (41)

References (26)
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  • 8
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    • 4b,c bonds
    • 4b,c bonds.
  • 9
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    • Harrison, P. G., Ed. Blackie: London
    • (b) Harrison, P. G. In Chemistry of Tin, Harrison, P. G., Ed. Blackie: London, 1989: p. 13.
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    • Stille, J.K. Angew. Chem. Int. Ed. Engl. 1986, 25, 508. For a review see: Farina, V.; Krishnamurthy, V.; Scott, W. J. In The Stille Reaction, Organic Reactions Vol. 50, Paquette, L. A., Ed.; Wiley: Chichester, 1997; p. 1
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 508
    • Stille, J.K.1
  • 14
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    • note
    • 3 in excess, and the ammonia was allowed to evaporate. The residue was dissolved with water, then extracted with diethyl ether. The product was quantified by GLC using the internal standard method. Spectroscopic data for the isolated product agreed with those reported in the literature, see ref. 8.
  • 15
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    • - ions in 1,2-dimethoxy-ethane to afford the substitution products (60-88%). No light was used to induce these reactions. See Yamamoto, Y.; Yanagi, A. Chem. Pharm. Bull. 1982, 30, 1731.
    • (1982) Chem. Pharm. Bull. , vol.30 , pp. 1731
    • Yamamoto, Y.1    Yanagi, A.2
  • 18
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    • Spectroscopic data for the isolated product agreed with those reported in the literature, see Kraus, C. A.; Sessions, W. J. Am. Chem. Soc. 1925, 47, 2361.
    • (1925) J. Am. Chem. Soc. , vol.47 , pp. 2361
    • Kraus, C.A.1    Sessions, W.2
  • 20
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    • and ref. 12
    • Spectroscopic data for the isolated product agreed with those reported in the literature, see Eunin, A. B.; Seyferth, D. J. Am. Chem. Soc. 1967, 89, 952, and ref. 12.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 952
    • Eunin, A.B.1    Seyferth, D.2
  • 21
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    • Spectroscopic data for the isolated product agreed with those reported in the literature, see ref. 8
    • Spectroscopic data for the isolated product agreed with those reported in the literature, see ref. 8.
  • 24
    • 0342659503 scopus 로고    scopus 로고
    • Spectroscopic data for the isolated product agreed with those reported in the literature, see ref. 17
    • Spectroscopic data for the isolated product agreed with those reported in the literature, see ref. 17.
  • 26
    • 0343093823 scopus 로고    scopus 로고
    • 2: C, 50.06; H, 4.96; Sn, 44.98. Found: C, 50.05; H, 5.21
    • 2: C, 50.06; H, 4.96; Sn, 44.98. Found: C, 50.05; H, 5.21.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.