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Volumn 6, Issue 16, 2008, Pages 2908-2913

Conformation and stereodynamics of 2,2′-disubstituted N,N′-diaryl ureas

Author keywords

[No Author keywords available]

Indexed keywords

METABOLISM; NUCLEAR MAGNETIC RESONANCE; UREA;

EID: 49149093636     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b802673d     Document Type: Article
Times cited : (32)

References (33)
  • 27
    • 0242490625 scopus 로고    scopus 로고
    • N,N′-Diaryl ureas exhibit a rich lithiation chemistry in which conformation may also play an important role; see:
    • T. L. Kurth F. D. Lewis J. Am. Chem. Soc. 2003 125 13760
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 13760
    • Kurth, T.L.1    Lewis, F.D.2
  • 33
    • 0002999412 scopus 로고
    • The assignment of anti stereochemistry to the major conformer remains tentative, though related di-ortho-substituted ureas (J. Clayden, and M. Pickworth, unpublished results) display endo,anti conformations in the solid state, as do all extended di-meta-substituted polyureas (ref. 9)
    • M. Oki Top. Stereochem. 1983 14 1
    • (1983) Top. Stereochem. , vol.14 , pp. 1
    • Oki, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.