Antimony chloride doped on hydroxyapetite catalyzed stereoselective one-pot synthesis of pyrano[3,2-c]quinolines

Tetrahedron Letters

Volumn 47, Issue 45, 2006, Pages 7919-7921

  Mahajan, Deepali ^a   Ganai, Bilal A ^a   Sharma, Rattan Lal ^a   Kapoor, Kamal K ^a  

^a UNIVERSITY OF JAMMU   (India)

Author keywords

Diels Alder; Heterogeneous catalyst; SbCl3 HAP; Solid supported; Stereoselective

Indexed keywords

ANILINE DERIVATIVE; ANTIMONY; BENZALDEHYDE DERIVATIVE; CHLORIDE; HYDROXYAPATITE; PYRAN DERIVATIVE; QUINOLINE DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; STEREOCHEMISTRY; SYNTHESIS;

BETULACEAE;

EID: 33749241668     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.09.007     Document Type: Article

References (23)

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23. Preparation of the catalyst: To an antimony(III) chloride (2.28 g, 10 mmol) solution in 100 mL of distilled water was added 60 g of hydroxyapatite powder. The mixture was stirred at room temperature for 5 h followed by the removal of water under reduced pressure. The resultant free flowing powder was then activated at 110 °C in an oven for 2 h and was used throughout the experimentation. Ganai, B. A. Ph.D. Thesis December 2005, University of Jammu, Jammu 180 006, India.