메뉴 건너뛰기




Volumn 71, Issue 2, 2006, Pages 504-511

Methyl ether derivatives of p-tert-butyl[3.1.3.1]homooxacalixarene. Formation, structure, and complexes with quaternary ammonium ions

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM COMPOUNDS; CONFORMATIONS; ETHERS; HYDROGEN BONDS; NUCLEAR MAGNETIC RESONANCE; SINGLE CRYSTALS; X RAY DIFFRACTION;

EID: 30744477752     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo051922t     Document Type: Article
Times cited : (26)

References (44)
  • 1
    • 0004146786 scopus 로고
    • The Royal Society of Chemistry: Cambridge, England
    • (a) Gutsche, C. D. Calixarenes; The Royal Society of Chemistry: Cambridge, England, 1989.
    • (1989) Calixarenes
    • Gutsche, C.D.1
  • 2
    • 0004268367 scopus 로고    scopus 로고
    • The Royal Society of Chemistry: Cambridge, England
    • (b) Gutsche, C. D. Calixarenes Revisited; The Royal Society of Chemistry: Cambridge, England, 1997.
    • (1997) Calixarenes Revisited
    • Gutsche, C.D.1
  • 5
    • 30744465887 scopus 로고    scopus 로고
    • Masci, B. In ref 1d
    • Masci, B. In ref 1d.
  • 9
    • 30744472592 scopus 로고    scopus 로고
    • note
    • 2 bridges; therefore, in the abridged names we use, the numbers in brackets are 3 or 1 and there is no need to explicitly indicate the number of aromatic rings, the number of oxygen atoms, or the location of the oxygen atom in the bridges. Moreover, we use the well-established term " homooxacalixarene" rather than the term "oxacalixarene", which could suggest the presence of O bridges by analogy with the important class of thiacalixarenes; see: Hosseini, M. W. In ref 1d.
  • 21
    • 0004266535 scopus 로고    scopus 로고
    • Mandolini, L., Ungaro, R., Eds.; Imperial College Press: London
    • Dalla Cort, A.; Mandolini, L. In Calixarenes in Action; Mandolini, L., Ungaro, R., Eds.; Imperial College Press: London, 2000.
    • (2000) Calixarenes in Action
    • Dalla Cort, A.1    Mandolini, L.2
  • 25
    • 20844455596 scopus 로고    scopus 로고
    • and references therein
    • Seri, N.; Biali, S. J. Org. Chem. 2005, 70, 5278 and references therein.
    • (2005) J. Org. Chem. , vol.70 , pp. 5278
    • Seri, N.1    Biali, S.2
  • 26
    • 0033538619 scopus 로고    scopus 로고
    • 1,2-Alternate and 1,4-alternate conformations are indicated by No et al. as COC-1,2-alternate and C-1,2-alternate, respectively. The naming system proposed in ref 2 is intended to be useful for the conformations of isosubstituted homooxacalix[4]arenes in general. Namely, analogous problems hold for [3.3.3.1]homooxacalixarenes and for [3.1.1.1]homooxacalixarenes. In the latter case, 1,2-alternate and 1,4-alternate conformations according to ref 2 are otherwise named 1,2-alternate A and 1,2-alternate B; see: Félix, S.; Ascenso, J. R.; Lamartine, R.; Pereira, J. L. C. Tetrahedron 1999, 55, 8539.
    • (1999) Tetrahedron , vol.55 , pp. 8539
    • Félix, S.1    Ascenso, J.R.2    Lamartine, R.3    Pereira, J.L.C.4
  • 42
    • 0003440472 scopus 로고    scopus 로고
    • Nonius B.V., Delft, The Netherlands
    • Kappa CCD Software, Nonius B.V., Delft, The Netherlands, 1998.
    • (1998) Kappa CCD Software


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.