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Volumn 63, Issue 2, 2004, Pages 241-247

Selective phototransformation of hydroxy-substituted aromatic nitrones into N,N-diarylformamide derivatives showing a novel conformational isomerism

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; AROMATIC NITRO COMPOUND; AROMATIC NITRONE DERIVATIVE; FORMAMIDE DERIVATIVE; NITROGEN; NITRONE DERIVATIVE; OXAZIRIDINE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

EID: 0842290667     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-03-9942     Document Type: Article
Times cited : (9)

References (20)
  • 12
    • 0842310229 scopus 로고    scopus 로고
    • note
    • 2: C, 77.96; H, 5.45; N, 5.05. Found: C, 78.26; H, 5.46; N, 5.43. Spectroscopic and physical properties of 1b-d will be given elsewhere.
  • 13
    • 0842310227 scopus 로고    scopus 로고
    • note
    • 2: C, 77.96; H, 5.45; N, 5.05. Found: C, 77.77; H, 5.48; N, 5.09. Spectroscopic data for 2b-d and 3d were consistent with their structures and will be given elsewhere.
  • 14
    • 85089110130 scopus 로고    scopus 로고
    • note
    • 2)= 0.1653.
  • 15
    • 0842331815 scopus 로고    scopus 로고
    • note
    • MM2 and PM5 calculations were accomplished by using CAChe 5.0 for Windows available from Fujitsu Ltd (2002).
  • 16
    • 0000887799 scopus 로고
    • Quantum yields were determined at low conversions (10-15%) of the starting I according to the method of Hatchard and Parker which employs a potassium trioxalatoferrate(III) actinometer (C. G. Hatchard and C. A. Parker, Proc. R. Soc. London, Ser. A, 1956, 235, 518). All the quantum yields are an average of more than five determinations.
    • (1956) Proc. R. Soc. London, Ser. A , vol.235 , pp. 518
    • Hatchard, C.G.1    Parker, C.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.