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Volumn 74, Issue 24, 2009, Pages 9513-9516

Stereochemical and conformational exchanges in N,N′-di(2-pyridyl) formamidines: An X-ray and 1H NMR study

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; CONFORMATIONAL EXCHANGE; FORMAMIDINES; HYDROGEN-BONDED DIMERS; NMR STUDIES; PYRIDYL; SOLID-STATE STRUCTURES; STATE ANALYSIS;

EID: 73149100600     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9020453     Document Type: Article
Times cited : (14)

References (41)
  • 24
    • 73149121989 scopus 로고    scopus 로고
    • 2 is reported to be stabilized when Ar = o-hydroxyphenyl, through a hydrogen bond between the hydroxyl function on the aryl group and the lone pair of the imino nitrogen covalently bound to the aryl ring. Kinetically produced Z N,N,N′-trisubstituted amidines and their isomerization to the stable E form are reported in: (a) Hegarthy, A. F.; Chandler, A. J. Chem. Soc., Chem. Commun. 1980, 131-132.
    • 2 is reported to be stabilized when Ar = o-hydroxyphenyl, through a hydrogen bond between the hydroxyl function on the aryl group and the lone pair of the imino nitrogen covalently bound to the aryl ring. Kinetically produced Z N,N,N′-trisubstituted amidines and their isomerization to the stable E form are reported in: (a) Hegarthy, A. F.; Chandler, A. J. Chem. Soc., Chem. Commun. 1980, 131-132.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.