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Volumn , Issue 7, 2007, Pages 754-756

Achieving conformational control over C-C, C-N and C-O bonds in biaryls, N,N′-diarylureas and diaryl ethers: Advantages of a relay axis

Author keywords

[No Author keywords available]

Indexed keywords

ETHER DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; UREA DERIVATIVE;

EID: 33846932037     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b614618j     Document Type: Article
Times cited : (23)

References (28)
  • 17
    • 0000902463 scopus 로고
    • Biaryls bearing only two ortho-substituents are not usually atropisomeric (however, see:
    • C. Agami T. Rizk Tetrahedron 1985 41 537
    • (1985) Tetrahedron , vol.41 , pp. 537
    • Agami, C.1    Rizk, T.2
  • 23
    • 0001651123 scopus 로고    scopus 로고
    • C-N bond rotation in N,N′-diarylureas may be slow on the NMR timescale, though N,N′-diarylureas are not generally atropisomeric. See:
    • G. Karig M.-T. Moon N. Thasana T. Gallagher Org. Lett. 2002 4 3115
    • (2002) Org. Lett. , vol.4 , pp. 3115
    • Karig, G.1    Moon, M.-T.2    Thasana, N.3    Gallagher, T.4
  • 28
    • 0035794259 scopus 로고    scopus 로고
    • 2OMe, Z = t-Bu), 623110 (4z, R = H) and 623110 (10y). For crystallographic data in CIF or other electronic format see DOI: For clarity and consistency of conformational representation, Fig. 1(b) shows a molecule enantiomeric with that described in the accompanying crystallographic data
    • J. Clayden L. W. Lai M. Helliwell Tetrahedron: Asymmetry 2001 12 695
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 695
    • Clayden, J.1    Lai, L.W.2    Helliwell, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.