Benign and highly efficient synthesis of indenoquinoline derivatives from 3-arylamino-5,5-dimethylcyclohex-2-enone, arylaldehyde and 1,3-indenedione in ionic liquid medium

Journal of Heterocyclic Chemistry

Volumn 45, Issue 1, 2008, Pages 71-76

  Wang, Xiang Shan ^a,b,c   Zhang, Mei Mei ^c   Zeng, Zhao Sen ^a   Shi, Da Qing ^a,c   Tu, Shu Jiang ^a,c   Wei, Xian Yong ^b   Zong, Zhi Min ^b  

^a JIANGSU NORMAL UNIVERSITY   (China)

^b CHINA UNIVERSITY OF MINING AND TECHNOLOGY   (China)

^c JIANGSU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 BUTYL 3 METHYLIMIDAZOLIUM TETRAFLUOROBORATE; 1,3 INDENEDIONE; 5,5 DIMETHYLCYCLOHEX 2 ENONE; ALDEHYDE DERIVATIVE; HETEROCYCLIC COMPOUND; INDENO[1,2 B]QUINOLINE DERIVATIVE; IONIC LIQUID; PROTON; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS; THIN LAYER CHROMATOGRAPHY; X RAY DIFFRACTION;

EID: 38949132212     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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18. -1. Intensity data were collected on Rigaku Mercury diffractometer with graphite monochromated MoKα radiation (λ = 0.71070Å) using ω scan mode with 3.01°<θ<25.25°. 4222 unique reflections were measured and 3385 reflections with I>2σ(I) were used in the refinement. Structure solved by direct methods and expanded using Fourier techniques. The final cycle of full-matrix least squares technique to R = 0.0618 and wR = 0.1494.