Effect of sodium naphthalenide, a key set reagent, on 3-substituted indoles

Heterocycles

Volumn 63, Issue 10, 2004, Pages 2371-2377

  Banerji, Avijit ^a   Bandyopadhyay, Debasish ^a   Basak, Bidyut ^a  

^a UNIVERSITY OF CALCUTTA   (India)

Author keywords

[No Author keywords available]

Indexed keywords

1,1 BIS(3 INDOLYL)ETHANE; 1,4 (3,3' DIINDOLYL) 1,4 DIOXOBUTANE; 3 (1 NAPHTHYLCARBONYL)INDOLE; 3 ACETYLINDOLE; 3 BENZOYLINDOLE; 3 BENZYLINDOLE; 3 ETHYLINDOLE; 3 FORMYLINDOLE; 3 TRIFLUOROACETYLINDOLE; 3,3' DIFORMYL 2,2' BIINDOYL; 8 (NAPHTH 1 YLMETHYL)INDOLE; BIS(3 INDOLYL) KETONE; INDOLE DERIVATIVE; NAPHTHALENIDE SODIUM; REAGENT; SKATOLE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTRON TRANSPORT; INFRARED SPECTROPHOTOMETRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 7044260877     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-04-10142     Document Type: Article

References (13)

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6. D. Bandyopadhyay, Ph. D. thesis, 2002, University of Calcutta, India.
7. α radiation (1.541 Å). The structure was solved by direct method and refined with isotropic, then anisotropic thermal factors by Full-Matrix-Least-Squares procedure. Crystallographic data for this structure have been deposited at the Cambridge Crystallographic Data Centre (CCDC 234174). Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44(O)-1223-336033 or email: deposit@ccdc.cam.ac.uk].
8. (a) J.H. Stocker and R.M. Jenevein, Chem. Commun., 1968, 934.
9. (b) H.O. House, Modern Synthetic Reactions (Second Edition), The Benjamin/Cummings Publishing Company, 1972, p. 161.
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12. M. Chakrabarty, N. Ghosh, R. Basak, and Y. Harigaya, Tetrahedron Lett., 2002, 43, 4075.
13. M. Chakrabarty, R. Basak, and Y. Harigaya, Heterocycles, 2001, 55, 2431.