Electrophile-induced domino cyclization reaction for the synthesis of 2,2a,10,11-tetrahydrofuro[2′,4′:4,6]pyrano[2,3-b]quinolines

Tetrahedron Letters

Volumn 49, Issue 45, 2008, Pages 6423-6425

  Singh, Bhawana ^a   Chandra, Atish ^a   Upadhyay, Shraddha ^a   Singh, Radhey M ^a   Puerta, M C ^b   Valerga, Pedro ^b  

^a BANARAS HINDU UNIVERSITY   (India)

^b UNIVERSITY OF CÁDIZ   (Spain)

Author keywords

3 Homoallyl 2 quinolones; Diastereomers; Domino process; Pyranoquinoline; Tetracyclic pyranoquinoline

Indexed keywords

2,2A,10,11 TETRAHYDROFURO[2',4':4,6]PYRANO[2,3 B]QUINOLINE DERIVATIVE; 3 HOMOALLYL 2 QUINOLONE DERIVATIVE; ACETIC ACID; IODINE; MERCURIC OXIDE; QUINOLINE DERIVATIVE; QUINOLONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL STRUCTURE; CYCLIZATION; MOLECULAR INTERACTION; SYNTHESIS;

EID: 52049118784     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.079     Document Type: Article

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25. 2: C, 73.23; H, 5.20; N, 6.57. Found: C, 72.89; H, 5.09; N, 6.45.
26. w = 0.1344. Crystallographic data (excluding structure factors) for the structures in this Letter have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 666668. Copies of the data can be obtained free of charge on an application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +441223 336033 or e-mail: deposit@ccdc.cam.ac.uk].