An efficient synthesis of indoloquinoline alkaloid - Neocryptolepine (cryptotackieine)

Tetrahedron Letters

Volumn 52, Issue 49, 2011, Pages 6594-6596

  Parvatkar, Prakash T ^a   Tilve, Santosh G ^a  

^a GOA UNIVERSITY   (India)

Author keywords

Alkaloid; Cryptotackieine; Indoloquinoline; Neocryptolepine; One pot and Wittig reaction

Indexed keywords

CRYPTOLEPINE; INDOLOQUINOLINE ALKALOID; INDOLOQUINOLINE DERIVATIVE; NEOCRYPTOLEPINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; ONE POT SYNTHESIS; SYNTHESIS; WITTIG REACTION;

EID: 80555150524     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.09.135     Document Type: Article

References (24)

1. G.L. Boye, and O. Ampofo K. Boakye-Yiadom, S.O.A. Bamgbose, Proceeding of the First International Symposium on Cryptolepine 1983 University of Science and Technology Ghana 37
2. B. Oliver-Bever Medicinal Plants in Tropical West Africa Vol. 131 1986 Cambridge University Press Cambridge 18
3. K.Q.J. Boakye-Yiadom Crude Drug Res. 17 1979 78
4. K. Cimanga, T. De Bruyne, L. Pieters, M. Claeys, and A. Vlietinck Tetrahedron Lett. 37 1996 1703
5. M.H.M. Sharaf, P.L. Schiff Jr., A.N. Tackie, C.H. Phoebe Jr., and G.E. Martin J. Heterocycl. Chem. 33 1996 239
6. K. Cimanga, T. De Bruyne, L. Pieters, and A.J. Vlietinck J. Nat. Prod. 60 1997 688
7. W. Peczynska-Czoch, F. Pognan, L. Kaczmarek, and J. Boratynski J. Med. Chem. 37 1994 3503
8. L. Kaczmarek, R. Balicki, P. Nantka-Namirski, W. Peczynska-Czoch, and M. Mordarski Arch. Pharm. 321 1998 463
9. M. Alajarin, P. Molina, and A. Vidal J. Nat. Prod. 60 1997 747
10. G. Timari, T. Soos, and G. Hajos Synlett 1997 1067
11. P. Molina, P.M. Fresneda, and S. Delgado Synthesis 1999 326
12. P.M. Fresneda, P. Molina, and S. Delgado Tetrahedron 57 2001 6197
13. C. Shi, Q. Zhang, and K.K. Wang J. Org. Chem. 64 1999 925
14. T.H.M. Jonckers, S. van Miert, K. Cimanga, C. Bailly, P. Colson, M.-C. De Pauw-Gillet, H. Van den Heuvel, M. Claeys, R. Dommisse, G.L.F. Lemiere, A. Vlietinck, and L. Pieters J. Med. Chem. 45 2002 3497
15. T.-L. Ho, and D.-G. Jou Helv. Chim. Acta 85 2002 3823
16. G.S.M. Sundaram, C. Venkatesh, U.K. Syam Kumar, H. Ila, and H. Junjappa J. Org. Chem. 69 2004 5760
17. T. Dhanabal, R. Sangeetha, and P.S. Mohan Tetrahedron 62 2006 6258
18. P.T. Parvatkar, P.S. Parameswaran, and S.G. Tilve Tetrahedron Lett. 48 2007 7870
19. S. Sharma, and B. Kundu Tetrahedron Lett. 49 2008 7062
20. P.T. Parvatkar, P.S. Parameswaran, and S.G. Tilve J. Org. Chem. 74 2009 8369
21. G.A. Kraus, and H. Guo Tetrahedron Lett. 51 2010 4137
22. M.J. Haddadin, R.M.B. Zerdan, M.J. Kurth, and J.C. Fettinger Org. Lett. 12 2010 5502
23. S. Hostyn, K.A. Tehrani, F. Lemiere, V. Smout, and B.U.W. Maes Tetrahedron 67 2011 655
24. P.T. Parvatkar, P.S. Parameswaran, and S.G. Tilve Curr. Org. Chem. 15 2011 1036