Synthesis of some analogues of (±)gelliusine F, (±)gelliusine E, and total synthesis of 2,2-di(6′-bromo-3′-indolyl)ethylamine

Tetrahedron Letters

Volumn 53, Issue 4, 2012, Pages 426-428

  Seetham Naidu, P ^a   Bhuyan, Pulak J ^a  

^a Medicinal Chemistry Division   (India)

Author keywords

( )Gelliusine E; ( )Gelliusine F; 2,2 Di(6 bromo 3 indolyl)ethylamine; 3,3 Diindolylmethane; Amino acetaldehyde dimethyl acetal; Phthalic anhydride

Indexed keywords

2,2 DI(6' BROMO 3' INDOLYL)ETHYLAMINE; ALKALOID DERIVATIVE; GELLIUSINE E; GELLIUSINE F; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; DEPROTECTION REACTION; DRUG SYNTHESIS; QUANTUM YIELD; REACTION ANALYSIS;

EID: 84929339481     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.11.063     Document Type: Article

References (25)

1. C.A. Bradfield, and L.F. Bjeldanes J. Agric. Food Chem. 35 1987 46
2. T.A. Broadbent, and H.S. Broadbent Curr. Med. Chem. 5 1998 337
3. T.A. Broadbent, and H.S. Broadbent Curr. Med. Chem. 5 1998 469
4. L. Xue, J.J. Pestka, L. Maoxiang, G.L. Firestone, and L.F. Bjeldanes J. Nutr. Biochem. 19 2008 336
5. J.E. Riby, L. Xue, U. Chatterji, E.L. Bjeldanes, G.L. Firestone, and L.F. Bjeldanes Mol. Pharmacol. 69 2006 430
6. K.M. Dalessandri, G.L. Firestone, M.D. Fitch, H.L. Bradlow, and L.F. Bjeldanes J. Nutr. Cancer - Int. J. 50 2004 161
7. C. Hong, G.L. Firestone, and L.F. Bjeldanes Biochem. Pharmacol. 63 2002 1085
8. H.T. Le, C.M. Schaldach, G.L. Firestone, and L.F. Bjeldanes J. Biol. Chem. 278 2003 21136
9. M.C. Bell, P. Crowley-Nowick, H.L. Bradlow, D.W. Sepkovic, D. Schmidt-Grimminger, P. Howell, E.J. Mayeaux, A. Tucker, E.A. Turbat-Herrera, and J.M. Mathis Gynecol. Oncol. 78 2000 123 129
10. K. McGuire, N. Ngoubilly, M. Neavyn, and S. Lanza-Jacoby J. Surg. Res. 132 2006 208
11. M. Shiri, M. Ali-Zolfigol, H.G. Kruger, and Z. Tanbakouchain Chem. Rev. 110 2010 2250
12. E. Fahy, B.C.M. Potts, D.J. Faulkner, and K. Smith J. Nat. Prod. 54 1991 564
13. G. Bifulco, I. Bruno, R. Riccio, J. Lavayre, and G. Bourdy J. Nat. Prod. 58 1995 1254
14. W. Gul, and T. Hamann Life Sci. 78 2005 442
15. H.C. Mauger, J.-N. Denis, M.-T. Pouchot, and Y. Vallee Tetrahedron 56 2000 791
16. j.-N. Denis, H. Mauger, and Y. Valle Tetrahedron Lett. 38 1997 8515
17. M. Chakrabarty, R. Basak, N. Ghosh, and Y. Harigaya Tetrahedron 60 2004 1941
18. M.L. Deb, and P.J. Bhuyan Tetrahedron Lett. 47 2006 1441
19. M.L. Deb, and P.J. Bhuyan Synlett 2008 325
20. M.L. Deb, and P.J. Bhuyan Synthesis 2008 286
21. M.L. Deb, and P.J. Bhuyan Tetrahedron Lett. 48 2007 2159
22. M.L. Deb, and P.J. Bhuyan Synthesis 2008 2891
23. M. Borgström, S. Ott, R. Lomoth, J. Bergquist, L. Hammarström, and O. Johansson Inorg. Chem. 45 2006 4820
24. M. Boisbrun, E. Vassileva, M. Raoul, J.-Y. Laronze, and J. Sapi Monatsh. Chem. 134 2003 1641
25. S.K. Adla, G. Gotz, P.G. Jones, and T. Lindel Synthesis 2010 2161