메뉴 건너뛰기




Volumn 46, Issue 23, 2007, Pages 4337-4341

Hexasilylated total carbomer of benzene

Author keywords

Alkynes; Aromaticity; Carbobenzene; Macrocyclization; Pericyclynes

Indexed keywords

AROMATICITY; CARBOBENZENE; MACROCYCLIZATION; PERICYCLYNES;

EID: 34447256320     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200605262     Document Type: Article
Times cited : (31)

References (32)
  • 4
    • 84891029339 scopus 로고    scopus 로고
    • Theoretical Studies on Acetylenic Scaffolds: R. Chauvin, C. Lepetit, Acetylene Chemistry: Chemistry, Biology and Material Science (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim, 2005, chap. 1, pp. 1-50.
    • "Theoretical Studies on Acetylenic Scaffolds": R. Chauvin, C. Lepetit, Acetylene Chemistry: Chemistry, Biology and Material Science (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim, 2005, chap. 1, pp. 1-50.
  • 16
    • 0037112596 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 4339-4343.
    • (2002) Chem. Int. Ed , vol.41 , pp. 4339-4343
    • Angew1
  • 17
    • 34447262646 scopus 로고    scopus 로고
    • Crystal data and structure refinement for 2b1: C 36H24O6·CH2Cl2, Mr, 637.51 g mol-1, crystal dimensions: 0.25 x 0.30 x 0.50 mm3, T, 180 K, trigonal, space group R3, a, 21.479(5, b, 21.479(5, c, 6.560(5) Å, α, 90, β, 90, γ, 180°, V, 2621(2) Å3, Z, 3, ρ, 1.21 g cm3, μ, 0.228 mm-1, 27 634 reflections measured, 1952 unique (R(int, 0.0200, θmax, 32.20°, index ranges: -31 ≤ h ≤ 31, 31 ≤ k ≤ 31, 9 ≤ l ≤ 9, σ(I) limit, 2.00, 70 refined parameters, 747 reflections used (I > 2σI, R1, 0.0720, wR2, 0.0834, Δρmin, 0.42 e Å-3, Δρmax, 0
    • -3, GOF = 1.127. CCDC-632362 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam. ac.uk/data_request/cif.
  • 18
    • 33845377321 scopus 로고    scopus 로고
    • For n = 5, see: K. N. Houk, L. T. Scott, N. G. Rondan, D. C. Spellmeyer, G. Reinhardt, J. L. Hyun, G. J. DeCicco, R. Weiss, M. H. M. Chen, L. S. Bass, J. Clardy, F. S. Jorgensen, T. A. Eaton, V. Sarkozi, C. M. Petit, L. Ng, K. D. Jordan, J. Am. Chem. Soc. 1985, 107, 6556-6562;
    • a) For n = 5, see: K. N. Houk, L. T. Scott, N. G. Rondan, D. C. Spellmeyer, G. Reinhardt, J. L. Hyun, G. J. DeCicco, R. Weiss, M. H. M. Chen, L. S. Bass, J. Clardy, F. S. Jorgensen, T. A. Eaton, V. Sarkozi, C. M. Petit, L. Ng, K. D. Jordan, J. Am. Chem. Soc. 1985, 107, 6556-6562;
  • 19
    • 34447253611 scopus 로고    scopus 로고
    • for n = 4, 6, 7, and 8, see: L. T. Scott, private communication;
    • b) for n = 4, 6, 7, and 8, see: L. T. Scott, private communication;
  • 23
    • 34447266504 scopus 로고    scopus 로고
    • H. Jiao, N. J. R. v. E. Hommes, P. von R. Schleyer, A. de Meijere, J. Org. Chem. 1996, 61, 2826-2828.
    • b) H. Jiao, N. J. R. v. E. Hommes, P. von R. Schleyer, A. de Meijere, J. Org. Chem. 1996, 61, 2826-2828.
  • 25
    • 34447286281 scopus 로고    scopus 로고
    • 1 under Hay oxidative-coupling conditions afforded a completely insoluble black solid.
    • 1 under Hay oxidative-coupling conditions afforded a completely insoluble black solid.
  • 32
    • 0031882648 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 161-164.
    • (1998) Chem. Int. Ed , vol.37 , pp. 161-164
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.