An aldol approach to the synthesis of the anti-tubercular agent erogorgiaene

Tetrahedron Letters

Volumn 48, Issue 16, 2007, Pages 2841-2843

  Yadav, J S ^a   Basak, A K ^a   Srihari, P ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DITERPENE; EROGORGIAENE; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; DIASTEREOISOMER; DRUG STRUCTURE; DRUG SYNTHESIS; FRIEDEL CRAFTS REACTION; STEREOCHEMISTRY;

EID: 33947223524     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.103     Document Type: Article

References (28)

1. Rodriguez A.D., and Ramirez C. J. Nat. Prod. 64 (2001) 101
2. Cesati R.R., de Armas J., and Hoveyda A.H. J. Am. Chem. Soc. 126 (2004) 96
3. Davies H.M.L., and Walji A.M. Angew. Chem., Int. Ed. 117 (2005) 1761
4. Harmata M., and Hong X. Tetrahedron Lett. 46 (2005) 3847
5. For recent work see:. Yadav J.S., Pratap I., and Tadi B.P. Tetrahedron Lett. 47 (2006) 3773
6. Yadav J.S., Srinivas R., and Sathaiah K. Tetrahedron Lett. 47 (2006) 1603
7. Yadav J.S., Raju A.K., Rao P.P., and Rajaiah G. Tetrahedron: Asymmetry 16 (2005) 3283
8. Yadav J.S., Reddy M.S., and Prasad A.R. Tetrahedron Lett. 46 (2005) 2133
9. For recent references on creating stereogenic centres at benzylic positions, see:. Harmata M., Hong X., and Barnes C.L. Tetrahedron Lett. 44 (2003) 7261
10. Kim S.-G., Kim J., and Jung H. Tetrahedron Lett. 46 (2005) 2437
11. Lu J., Xie X., Chen B., She X., and Pan X. Tetrahedron: Asymmetry 16 (2005) 1435 and references cited therein
12. Heckrodt T.J., and Mulzer J. J. Am. Chem. Soc. 125 (2003) 4680
13. Prasad M., Kim H.-Y., Har D., Repic O., and Blacklock T.J. Tetrahedron Lett. 39 (1998) 9369
14. Tredwell M., Tenza K., Pacheco M.C., and Gouverneur V. Org. Lett. 7 (2005) 4495
15. Heemstra J.M., Kerrigan S.A., Doerge D.R., Helferich W.G., and Boulanger W.A. Org. Lett. 8 (2006) 5441
16. Prasad M., Har D., Kim H.-Y., and Repic O. Tetrahedron Lett. 39 (1998) 7076
17. Omura K., and Swern D. Tetrahedron Lett. 34 (1978) 1651
18. Mancuso A.J., Brownfain D.S., and Swern D. J. Org. Chem. 43 (1978) 2480-2482
19. Delaunay D., Toupet L., and Corre M.L. J. Org. Chem. 60 (1995) 6604
20. Crimmins M.T., and Choudhary K. Org. Lett. 2 (2000) 775
21. Crimmins M.T., King B.W., and Tabet E.A. J. Am. Chem. Soc. 119 (1997) 7883
22. Mühlthau F., and Bach T. Synthesis (2005) 3428
23. Lindström U.M., and Somfai P. Synthesis (1997) 109
24. Lipshutz B.H., and Hackmann C. J. Org. Chem. 59 (1994) 7437
25. Lipshutz B.H., and Sengupta S. Org. React. 41 (1992) 135
26. Derguini F., Lorne R.B., and Lisrtumelle G. Tetrahedron Lett. 13 (1977) 1181
27. Derguini F., Besseière Y., and Lisrtumelle G. Synth. Commun. 11 (1981) 859
28. 1,2a,b