Efficient synthesis of biologically active (±)-confluentin and (±)-daurichromenic acid

Synthetic Communications

Volumn 36, Issue 22, 2006, Pages 3329-3334

  Lee, Yong Rok ^a   Wang, Xue ^a   Noh, Seok Kyun ^a   Lyoo, Won Seok ^a  

^a Yeungnam University   (South Korea)

Author keywords

Anti HIV agent; Confluentin; Daurichromenic acid

Indexed keywords

ACETIC ACID DERIVATIVE; CONFLUENTIN; DAURICHROMENIC ACID; ETHYLENEDIAMINE DERIVATIVE; ETHYLENEDIAMINE DIACETATE; HUMAN IMMUNODEFICIENCY VIRUS ANTIBODY; ORCINOL; PLANT EXTRACT; RHODODENDRON DAURICUM EXTRACT; UNCLASSIFIED DRUG;

ARTICLE; BIOLOGICAL ACTIVITY; CATALYST; DRUG POTENCY; DRUG SYNTHESIS; MEDICINAL PLANT; OXIDATION; RHODODENDRON DAURICUM;

EID: 33751095918     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600941224     Document Type: Article

References (25)

1. Iwata, N.; Wang, N.; Yao, X.; Kitanata, S. J. Nat. Prod. 2004, 67, 1106.
2. (a) Chinese Mareria Medica; Jiangsu New Medical College. Shanghai People's Pub. House: Shanghai, 1977; p. 2506;
3. (b) Yasuda, M.; Igarashi, H.; Kano, Y.; Konoshima, M. Shoyakugaku Zasshi 1984, 38, 346.
4. (a) Kashiwada, Y.; Yamazaki, K.; Ikeshiro, Y.; Yamasisbi, T.; Fujioka, T.; Milashi, K.; Mizuki, K.; Cosentino, L. M.; Fowke, K.; Morris-Natschke, S. L.; Lee, K.-H. Tetrahedron 2001, 57, 1559;
5. (b) Jpn. Kokai Tokkyo Koho, JP 82-28,080, 1982.
6. (a) Henry, G. E.; Jacobs, H. Tetrahedron 2001, 57, 5335;
7. (b) Chang, S.; Grubbs, R. H. J. Org. Chem. 1998, 63, 864;
8. (c) Saimoto, H.; Yoshida, K.; Murakami, T.; Morimoto, M.; Sashiwa, H.; Shigemasa, Y. J. Org. Chem. 1996, 61, 6768;
9. (d) North, J. T.; Kronenthal, D. R.; Pullockaran, A. J.; Real, S. D.; Chen, H. Y. J. Org. Chem. 1995, 60, 3397;
10. (e) Gabbut, C. D.; Hartley, D. J.; Hepworth, J. D.; Heron, B. M.; Kanjia, M.; Rahman, M. M. Tetrahedron 1994, 50, 2507;
11. (f) Tiabi, M.; Zamarlik, H. Tetrahedron 1991, 32, 7251;
12. (g) Cossy, J.; Rakotoarisoa, H.; Kahn, P.; Desmurs, J.-P. Tetrahedron Lett. 1998, 39, 9671;
13. (h) Portscheller, J. L.; Malinakova, H. C. Org. Lett. 2002, 4, 3679;
14. (i) Hsung, R. P.; Shen, H. C.; Douglas, C. J.; Morgan, C. D.; Degen, S. J.; Yao, L. J. J. Org. Chem. 1999, 64, 690;
15. (j) Gabbutt, C. D.; Hepworth, J. D.; Heron, B. M.; Rahman, M. M.; Coles, S. J.; Hursthouse, M. B. Tetrahedron 1999, 55, 10467;
16. (k) Yadav, J. S.; Reddy, B. V. S.; Rao, T. P. Tetrahedron 2003, 41, 7943;
17. (l) Nguyen, V. T. H.; Langer, P. Tetrahedron 2005, 46, 815.
18. Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
19. Hellwig, V.; Nopper, R.; Mauler, F.; Freitag, J.; Kai-Hui, D.; Stadler, M. Arch. Pharm. Med. Chem. 2003, 336, 119.
20. Kurdyumov, A. V.; Hsung, R. P.; Ihlen, K.; Wang, J. Org. Lett. 2003, 5, 3935.
21. Kang, Y.; Mei, Y.; Du, Y.; Jin, Z. Org. Lett. 2003, 5, 4481.
22. Hu, Y.; Harrison, T. J.; Wilson, P. D. J. Org. Chem. 2004, 69, 3782.
23. Lellouche, J.-P. J. Org. Chem. 2001, 66, 693.
24. (a) Paquette, L. A.; Efremov, I. J. Org. Chem. 2005, 70, 510;
25. (b) Nicolaou, K. C.; Rodríguez, R. M.; Mitchell, H. J.; Suzuki, H.; Fylaktakidou, K. C.; Baudoin, O.; van Delft, F. L. Chem. Eur. J. 2000, 6, 3095.