참고문헌 (18)

1. 10.1242/jeb.00602 Borovsky, D. Trypsin-modulating oostatic factor: a potential new larvicide for mosquito control. Journal of Experimental Biology, 2003, 206(21), 3869. 

   상세보기

2. 10.1096/fasebj.4.12.2394318 Borovsky, D.; Carlson, D.; Griffin, P.; Shabanowitz, J.; Hunt, D., Mosquito oostatic factor: a novel decapeptide modulating trypsin-like enzyme biosynthesis in the midgut. The FASEB Journal, 1990, 4(12), 3015. 

   상세보기

3. Borovsky, D.; Nauen, R. Biological and biochemical effects of organo-synthetic analogues of Trypsin Modulating Oostatic Factor (TMOF) on Aedes aegypti, Heliothis virescens and Plutella xylostella. PESTYCYDY-WARSZAWA-, 2007, 3, 17. 

4. 10.1021/ja963857y Bates, R.B.; Brusoe, K.G.; Burns, J.J.; Caldera, S.; Cui, W.; Gangwar, S.; Gramme, M.R.; McClure, K.J.; Gregory, P.; Schadow, H. Dolastatins., 26. Synthesis and Stereochemistry of Dolastatin 111a. J. Am. Chem. Soc., 1997, 119(9), 2111. 

   상세보기

5. 10.1016/S0040-4039(01)80647-X Ewing, W.R.; Harris, B.D.; Li, W.R.; Joullie, M.M. . Synthetic studies of didemnins. IV. Synthesis of the macrocycle. Tetrahedron Lett.,. [1989,] 30, 3757. 

   상세보기

6. 10.1016/0040-4039(96)01653-X Mutou, T.; Kondo, T.; Shibata, T.; Ojika, M.; Kigoshi, H.; Yamada, K. Synthesis of dolastatin G and nordolastatin G, cytotoxic 35- membered cyclodepsipeptides of marine origin. Tetrahedron Lett., 1996, 37(40), 7299. 

   상세보기

7. 10.1016/00404-0399(50)0923Z- Nakamura, M.; Shibata, T.; Nakane, K.; Nemoto, T.; Ojika, M.; Yamada, K. Stereochemistry and total synthesis of dolastatin E. Tetrahedron Lett., 1995, 36(28), 5059. 

   상세보기

8. 10.1021/jo00374a017 Pettit, G.R.; Holzapfel, C.W. Structural biochemistry. 25. Antineoplastic agents. 110. Synthesis of the dolastatin 3 isomer cyclo [L-Pro-L- Leu-L-Val-(R, S)-(gln) Thz-(gly) Thz]. J. Org. Chem., 1986, 51(24), 4580. 

   상세보기

9. 10.1021/ja00256a046 Rinehart, K.L.; Kishore, V.; Nagarajan, S.; Lake, R.J.; Gloer, J.B.; Bozich, F.A.; Li, K.M.; Maleczka, R.E., Jr.; Todsen, W.L. Total synthesis of didemnins A, B, and C. J. Am. Chem. Soc., 1987, 109, 6846. 

   상세보기

10. 10.1002/hlca.19830660742 Wenger, R.M., Synthesis of Cyclosporine. I. Synthesis of enantiomerically pure (2S, 3R, 4R, 6E)-3-hydroxy-4-methyl-2-methylamino-6- octenoic acid starting from tartaric acid. Helv. Chim. Acta, 1983, 66(7), 2308. 

    상세보기

11. 10.1021/ja00897a025 Merrifield, R.B. (1963). Solid phase peptide synthesis. I. The synthesis of a tetrapeptide. J. Am. Chem. Soc., 85(14), 2149. 

    상세보기

12. 10.1002/1521-3773(20020703)41:13<2307::AID-ANIE2307>3.0.CO;2-Y Thern, B.; Rudolph, J.; Jung, G., Total synthesis of the nematicidal cyclododecapeptide omphalotin A by using racemization-free triphosgene-mediated couplings in the solid phase. Angew. Chem., Int. Ed., 2002, 41, 2307. 

    상세보기

13. 10.1016/S0040-4039(02)00657-3 Thern, B.; Rudolph, J.; Jung, G., Triphosgene as highly efficient reagent for the solid-phase coupling of N-alkylated amino acids-total synthesis of cyclosporin O. Tetrahedron Lett., 2002, 43(28), 5013. 

    상세보기

14. 10.1111/j.1399-3011.1991.tb00769.x Barlos, K.; Chatzi, O.; Gatos, D. ; Stavropoulos, G. 2-Chlorotrityl chloride resin. Studies on anchoring of Fmoc-amino acids and peptide cleavage. Int. J. Pept. Protein Res., 1991, 37(6), 513. 

    상세보기

15. 10.1016/j.tet.2004.01.020 Han, S.Y.; Kim, Y.A., Recent development of peptide coupling reagents in organic synthesis. Tetrahedron, 2004, 60(11), 2447. 

    상세보기

16. 10.1093/oso/9780199637256.001.0001 Chan, W.C. a. W., P.D., Fmoc Solid Phase Peptide Synthesis: A practical approach; 2000.Oxford University Press: New York,. 

    

17. 10.1002/chem.200900614 Subiros-Funosas, R.; Prohens, R.; Barbas, R.; El-Faham, A.; Albericio, F. Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion [1]. Chemistry-a European Journal, 2009, 15(37), 9394. 

    상세보기

18. Vojkovsky, T. (1995). Detection of secondary amines on solid phase. Pept. Res.,1995, 8(4), 236.