4-Methyl-3,4-dihydrospiro[cycloheptane-1′,2(1H)-quinoline]and 4-Methyl-3,4-dihydrospiro[cyclooctane-1′,2(1H)-quinoline]. Synthesis of Derivatives and Chemical Transformations

Journal of Heterocyclic Chemistry

Volumn 35, Issue 1, 1998, Pages 183-188

  Palma, Alirio ^a   Rozo, Wilson ^a   Stashenko, Elena ^a   Molina, Daniel ^a   Kouznetsov, Vladimir ^a  

^a UNIVERSIDAD INDUSTRIAL DE SANTANDER   (Colombia)

Author keywords

[No Author keywords available]

Indexed keywords

4 METHYL 3,4 DIHYDROSPIRO(CYCLOHEPTANE 1',2(1H) QUINOLINE); 4 METHYL 3,4 DIHYDROSPIRO(CYCLOOCTANE 1',2(1H) QUINOLINE); CYCLOALKANE DERIVATIVE; CYCLOHEPTANE DERIVATIVE; HETEROCYCLIC AMINE; OCTANE; QUINOLINE DERIVATIVE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DRUG ACETYLATION; DRUG SYNTHESIS; DRUG TRANSFORMATION; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; NITRATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

EID: 0031894790     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570350135     Document Type: Article

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28. The synthesis of imines 1-9 was realized using standard procedures, heating equimolar quantities of the reagents in toluene in the presence of glacial acetic acid (see, for example, ref 18).