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Volumn 64, Issue 15, 1999, Pages 5524-5529

The CH by N replacement effects on the aromaticity and reactivity of phosphinines

Author keywords

[No Author keywords available]

Indexed keywords

1,2 AZAPHOSPHININE; 1,3 AZAPHOSPHININE; 1,3,2 DIAZAPHOSPHININE; 1,3,5 DIAZAPHOSPHININE; AMPHOLYTE; NITROGEN; PHOSPHINE DERIVATIVE; PHOSPHORUS; UNCLASSIFIED DRUG;

EID: 0033597732     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9903611     Document Type: Article
Times cited : (61)

References (59)
  • 29
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    • (a) A 1,2-azaphosphinine has also been obtained by flash vaccuum pyrolysis; see: Bourdieu, C.; Foucaud, A. Tetrahedron Lett. 1987, 28, 4673.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 4673
    • Bourdieu, C.1    Foucaud, A.2
  • 37
    • 85069247451 scopus 로고    scopus 로고
    • note
    • As indicated in ref 11d, AM1 calculations have been performed on 1,3-aza- and 1,3,5-diazaphosphinines. To the best of our knowledge, this work was not reported.
  • 39
    • 85069258813 scopus 로고    scopus 로고
    • Schoeller, W. In ref 2, p 5
    • Schoeller, W. In ref 2, p 5.
  • 42
    • 0030445094 scopus 로고    scopus 로고
    • NICS values have been used to estimate aromaticity of various systems; see, for example: (a) Jiao, H. Schleyer, P. v. R. Angew. Chem., Int. Ed. Engl. 1996, 35, 2383. (b) Subramanian, G.; Schleyer, P. v. R.; Jiao, H. Angew. Chem., Int. Ed. Engl. 1996, 35, 2638. (c) Jiao, H. Schleyer,; P. v. R.; Mo, Y.; Allister, M. A.; Tidwell, T. J. Am. Chem. Soc. 1997, 119, 7075. (d) Tokitoh, N.; Wakita, K.; Okazaki, R.; Nagase, S.; Schleyer, P. v. R.; Jiao, H. J. Am. Chem. Soc. 1997, 119, 6951.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 2383
    • Jiao, H.1    Schleyer, P.V.R.2
  • 43
    • 0030457576 scopus 로고    scopus 로고
    • NICS values have been used to estimate aromaticity of various systems; see, for example: (a) Jiao, H. Schleyer, P. v. R. Angew. Chem., Int. Ed. Engl. 1996, 35, 2383. (b) Subramanian, G.; Schleyer, P. v. R.; Jiao, H. Angew. Chem., Int. Ed. Engl. 1996, 35, 2638. (c) Jiao, H. Schleyer,; P. v. R.; Mo, Y.; Allister, M. A.; Tidwell, T. J. Am. Chem. Soc. 1997, 119, 7075. (d) Tokitoh, N.; Wakita, K.; Okazaki, R.; Nagase, S.; Schleyer, P. v. R.; Jiao, H. J. Am. Chem. Soc. 1997, 119, 6951.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 2638
    • Subramanian, G.1    Schleyer, P.V.R.2    Jiao, H.3
  • 44
    • 1842333329 scopus 로고    scopus 로고
    • NICS values have been used to estimate aromaticity of various systems; see, for example: (a) Jiao, H. Schleyer, P. v. R. Angew. Chem., Int. Ed. Engl. 1996, 35, 2383. (b) Subramanian, G.; Schleyer, P. v. R.; Jiao, H. Angew. Chem., Int. Ed. Engl. 1996, 35, 2638. (c) Jiao, H. Schleyer,; P. v. R.; Mo, Y.; Allister, M. A.; Tidwell, T. J. Am. Chem. Soc. 1997, 119, 7075. (d) Tokitoh, N.; Wakita, K.; Okazaki, R.; Nagase, S.; Schleyer, P. v. R.; Jiao, H. J. Am. Chem. Soc. 1997, 119, 6951.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7075
    • Jiao, H.1    Schleyer, P.V.R.2    Mo, Y.3    Allister, M.A.4    Tidwell, T.5
  • 45
    • 0030859173 scopus 로고    scopus 로고
    • NICS values have been used to estimate aromaticity of various systems; see, for example: (a) Jiao, H. Schleyer, P. v. R. Angew. Chem., Int. Ed. Engl. 1996, 35, 2383. (b) Subramanian, G.; Schleyer, P. v. R.; Jiao, H. Angew. Chem., Int. Ed. Engl. 1996, 35, 2638. (c) Jiao, H. Schleyer,; P. v. R.; Mo, Y.; Allister, M. A.; Tidwell, T. J. Am. Chem. Soc. 1997, 119, 7075. (d) Tokitoh, N.; Wakita, K.; Okazaki, R.; Nagase, S.; Schleyer, P. v. R.; Jiao, H. J. Am. Chem. Soc. 1997, 119, 6951.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6951
    • Tokitoh, N.1    Wakita, K.2    Okazaki, R.3    Nagase, S.4    Schleyer, P.V.R.5    Jiao, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.