Lanthanide chloride catalyzed imino Diels-Alder reaction. One-pot synthesis of pyrano[3,2-c]- and furo[3,2-c]quinolines

Journal of Organic Chemistry

Volumn 64, Issue 17, 1999, Pages 6462-6467

  Ma, Yun ^a   Qian, Changtao ^a   Xie, Meihua ^b   Sun, Jie ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b ANHUI NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

FURO[3,2 C]QUINOLINE; LANTHANIDE; LANTHANIDE CHLORIDE; NATURAL PRODUCT; PYRANO[3,2 C]QUINOLINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIINFLAMMATORY ACTIVITY; ARTICLE; CATALYSIS; CRYSTAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; ESTROGEN ACTIVITY; INFRARED SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS;

EID: 0033588330     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982220p     Document Type: Article

References (42)

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40. ω = 0.043. Max/min peaks in final difference map, 0.36/-0.22. All calculations were performed using the TEXSAN crystallographic software package of Molecular Structure Corp.
41. ω = 0.043. Max/min peaks in final difference map 0.2/-0.12. All calculations were performed using the TEXSAN crystallographic software package of Molecular Structure Corporation.
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