JOURNAL BROWSE
Search
Advanced SearchSearch Tips
The First Synthesis of 3-epi-Xestoaminol C
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
The First Synthesis of 3-epi-Xestoaminol C
Choi, Jihye; Ha, Hyun-Joon;
  PDF(new window)
 Keywords
Synthesis;Xestoaminol C;3-epi-Xestoaminol C;Aziridine;Stereoselective reduction;
 Language
English
 Cited by
1.
Asymmetric synthesis of N,O-diacetyl-3-epi-xestoaminol C: structure and absolute configuration confirmation of 3-epi-xestoaminol C, Tetrahedron Letters, 2016, 57, 11, 1270  crossref(new windwow)
2.
Simple marine 1-deoxysphingoid bases: biological activity and syntheses, Tetrahedron: Asymmetry, 2016, 27, 24, 1187  crossref(new windwow)
3.
Total synthesis and the anticancer activity of (+)-spisulosine, Carbohydrate Research, 2016, 435, 26  crossref(new windwow)
4.
The convergent total synthesis of cytotoxic homospisulosine and its 3-epi-analogue, Tetrahedron: Asymmetry, 2015, 26, 24, 1394  crossref(new windwow)
 References
1.
Thudichum, J. L. W. 1884. A Treatise on the Chemical Constitution of Brain. Bailliere, Tindall, and Cox, London.

2.
(a) Pruett, S. T.; Bushnev, A. B.; Hagedorn, K.; Adiga M.; Haynes, C. A.; Sullards, M. C.; Liotta, D. C.; Merrill, A. H., Jr. J. Lipid Res. 2008, 49, 1621. crossref(new window)

3.
(b) Merrill, A. H., Jr. Chem. Rev. 2011, 111, 6387. crossref(new window)

4.
(c) Strub, G. M.; Maceyka, M.; Hait, N. C.; Milstien, S.; Spiegel, S. Adv. Exp. Med. Biol. 2010, 688, 141. crossref(new window)

5.
(d) Yang, Y.; Uhlig S. Ther. Adv. Respir. Dis. 2011, 5, 325. crossref(new window)

6.
(e) Tidhar, R.; Futerman, A. H. Biochim. Biophys. Acta. 2013, 1833, 2511. crossref(new window)

7.
(f) Siow, D.; Sunkara, M.; Morris A.; Wattenberg, B. Adv. Biol. Regul. 2015, 57, 42. crossref(new window)

8.
(a) Li, L.; Wang, L.; Shangguan, D.; Wei, Y.; Han, J.; Xiong, S.; Zhao, Z. J. Chromatogr. A. 2015, 1381, 140. crossref(new window)

9.
(b) Gendron, D.; Lemay, A.-M.; Tremblay, C.; Lai, L. J.; Langlois, A.; Bernatchez, É.; Flamand, N.; Blanchet, M.-R.; Don, A. S.; Bossé, Bissonnette, É.; Marsolais, D. Respir. Res. 2015, 16, 1. crossref(new window)

10.
(c) Nema, R.; Kumar, A. J. Cell Biol. 2015, 3, 1. crossref(new window)

11.
(a) Yun, J. M.; Sim, T. B.; Hahm, H. S.; Lee, W. K.; Ha, H.-J. J. Org. Chem. 2003, 68, 7675. crossref(new window)

12.
(b) Amarante, G. W.; Cavallaro, M.; Coelho, F. Tetrahedron Lett. 2010, 51, 2597. crossref(new window)

13.
(c) Xu, K.; Lai, G.; Zha, Z.; Pan, S.; Chen, H.; Wang, Z. Chem. Eur. J. 2012, 18, 12357. crossref(new window)

14.
(d) Ghosal, P.; Shaw, A. K. Tetrahedron Lett. 2010, 4140.

15.
(e) Malik, G.; Estéoule, A.; Retailleau, P.; Dauvan, P. J. Org. Chem. 2011, 76, 7438. crossref(new window)

16.
(f) Calder, E. D. D.; Zaed, A. M.; Sutherland, A. J. Org. Chem. 2013, 78, 7223. crossref(new window)

17.
(a) Chen, B.-S.; Yang, L.-H.; Ye, J.-L.; Huang, T.; Ruan, Y.-P.; Fu, J.; Huang, P.-Q. Eur. J. Med. Chem. 2011, 46, 5480. crossref(new window)

18.
(b) Ait-Youcef, R.; Moreau, X.; Greck, C. J. Org. Chem. 2010, 75, 5312. crossref(new window)

19.
(c) Zaed, A. M.; Sutherland, A. Org. Biomol. Chem., 2011, 9, 8030. crossref(new window)

20.
(d) Reddy, T. V. K.; Devi, B. L. A. P.; Prasad, R. B. N.; Sujitha, P.; Kumar, C. G. Eur. J. Med. Chem. 2013, 67, 384. crossref(new window)

21.
(a) Abraham, E.; Davis, S. G.; Millican, N. L.; Nicholson, R. L.; Roberts, P. M.; Smith, A. D. Org. Biomol. Chem., 2008, 6, 1655. crossref(new window)

22.
(b) Uraguchi, D.; Nakamura, S.; Ooi, T. Angew. Chem. Int. Ed. 2010, 49, 7562. crossref(new window)

23.
(c) Ichihashi, M.; Mori, K. Biosci. Biotechnol. Biochem. 2003, 67, 329. crossref(new window)

24.
(d) Jiménez, C.; Crews, P. J. Nat. Prod. 1990, 53, 978. crossref(new window)

25.
(a) Pelss, A.; Koskinen, A. M. P. Chem. Heterocycl. Compd. 2013, 49, 226. crossref(new window)

26.
(b) Garrido, L.; Zubía, E.; Ortega, M. J.; Naranjo, S.; Salvá, J. Tetrahedron Lett. 2001, 57, 4579. crossref(new window)

27.
Dasyam. N.; Munkacsi. A. B.; Fadzilah N. H.; Senanayake D. S.; O’Toole R. F. Keyzers R. A. J. Nat. Prod. 2014, 77, 1519. crossref(new window)

28.
Kim, Y. E.; Kang, L.-S.; Ha, H.-J.; Ko, S. W.; Lee, W. K. Heterocycles. 2007, 71, 2243. crossref(new window)