Stereoselective synthesis of the C1-C12 fragment of the thuggacins

Tetrahedron Asymmetry

Volumn 20, Issue 17, 2009, Pages 2027-2032

  Tang, Shoubin ^a   Xu, Zhengshuang ^a,b   Ye, Tao ^a,b  

^a Graduate School at Shenzhen   (China)

^b HONG KONG POLYTECHNIC UNIVERSITY   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; THIAZOLE; THUGGACIN A; THUGGACIN B; THUGGACIN C; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; ASYMMETRIC SYNTHESIS; CONTROLLED STUDY; DRUG STRUCTURE; DRUG SYNTHESIS; HORNER WADSWORTH EMMONS REACTION; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 70349203783     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.08.015     Document Type: Article

References (31)

1. Steinmetz H., Irschik H., Kunze B., Reichenbach H., Hofle G., and Jansen R. Chem. Eur. J. 13 (2007) 5822-5832
2. Irschik H., Reichenbach H., Hofle G., and Jansen R. J. Antibiot. 60 (2007) 733-738
3. Bock M., Miller R., Buntin K., and Kirschning A. Angew. Chem., Int. Ed. 47 (2008) 2308-2311
4. Bock M., Dehn R., and Kirschning A. Angew. Chem., Int. Ed. 47 (2008) 9134-9137
5. Li S., Liang S., Tan W.F., Xu Z.S., and Ye T. Tetrahedron 65 (2009) 2695-2702
6. Ren Q., Dai L., Zhang H., Tan W., Xu Z.S., and Ye T. Synlett (2008) 2379-2383
7. Li S., Liang S., Xu Z.S., and Ye T. Synlett (2008) 569-574
8. Chen Z., and Ye T. New J. Chem. 30 (2006) 518-520
9. Pang H.W., Xu Z.S., Chen Z.Y., and Ye T. Lett. Org. Chem. 2 (2005) 699-702
10. Pang H.W., Xu Z.S., and Ye T. Lett. Org. Chem. 2 (2005) 703-706
11. Xu Z.S., and Ye T. Tetrahedron: Asymmetry 16 (2005) 1905-1912
12. Chen H.L., Xu Z.S., and Ye T. Tetrahedron (2005) 11132-11140
13. Chen Z.Y., and Ye T. Synlett (2005) 2781-2785
14. Xu Z.S., Chen Z.Y., and Ye T. Tetrahedron: Asymmetry 15 (2004) 355-363
15. Peng Y.G., Pang H.W., and Ye T. Org. Lett. 6 (2004) 3781-3784
16. Chen Z.Y., Deng J.G., and Ye T. ARKIVOC Part VII (2003) 268-285
17. Xu Z.S., Peng Y.G., and Ye T. Org. Lett. 5 (2003) 2821-2824
18. Evans D.A., and Shih T.L. J. Am. Chem. Soc. 103 (1981) 2127-2129
19. Reddy Y.K., and Falck J.R. Org. Lett. 4 (2002) 969-971
20. Paquette L.A., Duan M., Konetzki I., and Kempmann C. J. Am. Chem. Soc. 124 (2002) 4257-4270
21. Smith A.B., and Ott G.R. J. Am. Chem. Soc. 120 (1998) 3935-3948
22. Marshall J.A., Eidam P., and Eidam H.S. J. Org. Chem. 71 (2006) 4840-4844
23. Midland M.M., Macdowell D.C., Hatch R.L., and Tramontano A. J. Am. Chem. Soc. 102 (1980) 867-869
24. Midland M.M., and Tramontano A. J. Org. Chem. 43 (1978) 1470-1471
25. 20 = + 16.6 (c 1.04, EtOH) (Yang, D.; Zhang, Y. H.; Zhang, D. W. J. Org. Chem. 2004, 69, 7577-7581).{A figure is presented}
26. Dess D.B., and Martin J.C. J. Org. Chem. 48 (1983) 4155-4156
27. Allali H., Tabti B., Alexandre C., and Huet F. Tetrahedron: Asymmetry 15 (2004) 1331-1333
28. Rega M., Candal P., Jimenez C., and Rodriguez J. Eur. J. Org. Chem. 6 (2007) 934-942
29. Bredenkamp M.W., Holzapfel C.W., and Van Zyl W.J. Synth. Commun. 20 (1990) 2235-2238
30. Dondoni A., and Merino P. Comprehensive Heterocyclic Chemistry II Vol. 3 (1996), Pergamon pp 432-434
31. Zhang H.X., Guibe F., and Balavoine G. J. Org. Chem. 55 (1990) 1857-1867