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Volumn 2, Issue 15, 2000, Pages 2335-2337

Solvent-dependent stabilization of the E configuration of propargylic secondary amides

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; CHLOROFORM; SOLVENT; WATER;

EID: 0034720952     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006096j     Document Type: Article
Times cited : (46)

References (28)
  • 2
    • 0001195982 scopus 로고
    • Examples of the use of model systems to examine noncovalent interactions: (a) Leonard, N. J. Acc. Chem. Res. 1979, 12, 423.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 423
    • Leonard, N.J.1
  • 14
    • 0030834850 scopus 로고    scopus 로고
    • For leading references on the hydrophobic effect, see: (a) Schellman, J. A. Biophys. J. 1997, 73, 2960.
    • (1997) Biophys. J. , vol.73 , pp. 2960
    • Schellman, J.A.1
  • 25
    • 0042881758 scopus 로고    scopus 로고
    • note
    • See ref 3a and citations therein.
  • 26
    • 0042881759 scopus 로고    scopus 로고
    • note
    • We examined compounds 4 to ensure that similar behavior would be seen when the naphthyl group of 3 was replaced with another hydrophobic group.
  • 27
    • 0002334268 scopus 로고    scopus 로고
    • Reference 5b shows that the E/Z rotamer ratios of simple secondary amides are not strongly affected by solvation. See also: Morgan, K. M.; Kopp, D. A. J. Chem. Soc., Perkin Trans. 2 1998, 2759.
    • (1998) J. Chem. Soc., Perkin Trans. 2 , pp. 2759
    • Morgan, K.M.1    Kopp, D.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.