Pure and Applied Chemistry

Pure Appl. Chem., 2012, Vol. 84, No. 6, pp. 1435-1443

http://dx.doi.org/10.1351/PAC-CON-11-08-24

Published online 2012-02-14

Studies toward the total synthesis of naturally occurring pyranonaphthoquinones from Ventilago harmandiana

References

• 1. R. G. Cooke, R. L. Johnson. Aust. J. Chem. 16, 695 (1963). (http://dx.doi.org/10.1071/CH9630695)
• 2. T. Smitinand. Thai Plant Names (Botanical Names-Vernacular Names), p. 547, The Forest Herbarium, Royal Forest Department, Thailand, Bangkok (2001).
• 3. A. Panthong, D. Kanjanapothi, T. Taesotikul, A. Phankummoon, K. Panthong, V. Reutrakul. J. Ethnopharmacol. 91, 237 (2004). (http://dx.doi.org/10.1016/j.jep.2003.12.025)
• 4. M. A. Brimble, L. J. Duncalf, M. R. Nairn. Nat. Prod. Rep. 16, 267 (1999). (http://dx.doi.org/10.1039/a804287j)
• 5. R. G. F. Giles, I. R. Green, N. V. Eeden. Synthesis 10, 1601 (2004).
• 6. W. H. Yeo, B. S. Yun, N. I. Back, Y. H. Kim, S. S. Kim, E. K. Park, K. S. Whang, S. H. Yu. J. Antibiot. 50, 546 (1997).
• 7. G. N. Krishnakumari, B. Bhuvaneswari, I. R. Swapna. Fitoterapia 72, 671 (2001). (http://dx.doi.org/10.1016/S0367-326X(01)00280-5)
• 8. M. A. Brimble. Pure Appl. Chem. 72, 1635 (2000). (http://dx.doi.org/10.1351/pac200072091635)
• 9. M. A. Brimble, M. R. Nairn, H. Prabaharan. Tetrahedron 56, 1937 (2000). (http://dx.doi.org/10.1016/S0040-4020(99)01021-2)
• 10. T. Hansen, S. L. Krintel, K. Daasbjerg, T. Skrydstrup. Tetrahedron Lett. 40, 6087 (1999). (http://dx.doi.org/10.1016/S0040-4039(99)01266-6)
• 11. P. P. Deshpande, K. N. Price, D. C. Baker. J. Org. Chem. 61, 455 (1996). (http://dx.doi.org/10.1021/jo951602h)
• 12. P. Deelertpaiboon, V. Reutrakul, S. Jarussophon, P. Tuchinda, C. Kuhakarn, M. Pohmakotr. Tetrahedron Lett. 50, 6233 (2009). (http://dx.doi.org/10.1016/j.tetlet.2009.09.036)
• 13. C. J. Rohbogner, G. C. Clososki, P. Knochel. Angew. Chem., Int. Ed. 47, 1503 (2008). (http://dx.doi.org/10.1002/anie.200703382)
• 14. H. Ren, A. Krasovskiy, P. Knochel. Chem. Commun. 543 (2005). (http://dx.doi.org/10.1039/b415588b)
• 15. K. Hisler, R. Tripoli, J. A. Murphy. Tetrahedron Lett. 47, 6293 (2006). (http://dx.doi.org/10.1016/j.tetlet.2006.06.118)
• 16. G. K. Cheung, I. M. Downie, M. J. Earle, H. Heaney, M. F. S. Matough, K. F. Shuhaibar, D. Thomas. Synlett 77 (1992). (http://dx.doi.org/10.1055/s-1992-21272)
• 17. V. Srivastava, M. P. Darokar, A. Fatima, J. K. Kumar, C. Chowdhury, H. O. Saxena, G. R. Dwivedi, K. Shrivastava, V. Gupta, S. K. Chattopadhyay, S. Luqman, M. M. Gupta, A. S. Negi, S. P. S. Khanuja. Bioorg. Med. Chem. 15, 518 (2007). (http://dx.doi.org/10.1016/j.bmc.2006.09.034)
• 18. F. Saito, K. Kuramochi, A. Nakazaki, Y. Mizushina, F. Sugawara, S. Kobayashi. Eur. J. Org. Chem. 4796 (2006). (http://dx.doi.org/10.1002/ejoc.200600702)
• 19. F. D. Boyer, I. Hanna. Org. Lett. 9, 2293 (2007). (http://dx.doi.org/10.1021/ol070708j)
• 20. J. Hine, J. J. Porter. J. Am. Chem. Soc. 79, 5493 (1957). (http://dx.doi.org/10.1021/ja01577a045)
• 21. V. Reutrakul, T. Thongpaisanwong, P. Tuchinda, C. Kuhakarn, M. Pohmakotr. J. Org. Chem. 69, 6913 (2004). (http://dx.doi.org/10.1021/jo0489768)
• 22. K. C. Nicolaou, C. J. N. Mathison, T. Montagnon. Angew. Chem., Int. Ed. 42, 4077 (2003). (http://dx.doi.org/10.1002/anie.200352076)
• 23. S. Claessens, J. Jacobs, N. D. Kimpe. Synlett 5, 741 (2007).
• 24. D. Mal, S. Ray, I. Sharma. J. Org. Chem. 72, 4981 (2007). (http://dx.doi.org/10.1021/jo062271j)
• 25. M. H. Ali, M. Niedbalski, G. Bohnert, D. Bryant. Synth. Commun. 36, 1751 (2006). (http://dx.doi.org/10.1080/00397910600616859)