Synthesis of glycyl-(S)-5-hydroxynorvaline
- 作者: Chulakov E.N.1, Tumashov A.A.1, Gruzdev D.A.1, Levit G.L.1, Krasnov V.P.1
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隶属关系:
- Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
- 期: 卷 59, 编号 11 (2023)
- 页面: 1507-1512
- 栏目: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/247269
- DOI: https://doi.org/10.31857/S0514749223110149
- EDN: https://elibrary.ru/NDGSMP
- ID: 247269
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作者简介
E. Chulakov
Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
Email: chulakov@ios.uran.ru
A. Tumashov
Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
D. Gruzdev
Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
G. Levit
Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
V. Krasnov
Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
参考
- Carmo-Silva A.E., Keys A.J., Beale M.H., Ward J.L., Baker J.M., Hawkins N.D., Arrabaça M.C., Parry M.A.J. Phytochemistry. 2009, 70, 664-671. doi: 10.1016/j.phytochem.2009.03.001
- Yan J., Lipka A.E., Schmelz E.A., Buckler E.S., Jander G. J. Exp. Bot. 2015, 66, 593-602. doi: 10.1093/jxb/eru385
- Ayala A., Cutler R.G. Free Radical Biol. Med. 1996, 21, 65-80. doi: 10.1016/0891-5849(95)02220-1
- Hannachi J.-C., Vidal J., Mulatier J.-C., Collet A. J. Org. Chem. 2004, 69, 2367-2373. doi: 10.1021/jo035700b
- Elbatrawi Y.M., Kang C.W., Del Valle J.R. Org. Lett. 2018, 20, 2707-2710. doi: 10.1021/acs.orglett.8b00912
- Krasnov V.P., Levit G.L., Musiyak V.V., Gruzdev D.A., Charushin V.N. Pure Appl. Chem. 2020, 92, 1277-1295. doi: 10.1515/pac-2019-1214
- Olsen R.K., Ramasamy K., Emery T. J. Org. Chem. 1984, 49, 3527-3534. doi: 10.1021/jo00193a016
- García M., Serra A., Rubiralta M., Diez A., Segarra V., Lozoya E., Ryder H., Palacios J.M. Tetrahedron Asymmetry. 2000, 11, 991-994. doi: 10.1016/S0957-4166(00)00020-3
- Wang L., Zha Z., Qu W., Qiao H., Lieberman B.P., Plössl K., Kung H.F. Nucl. Med. Biol. 2012, 39, 933-943. doi: 10.1016/j.nucmedbio.2012.03.007
- Longobardo L., Cecere N., DellaGreca M., de Paola I. Amino Acids. 2013, 44, 443-448. doi: 10.1007/s00726-012-1352-5
- Muetterties C., Janiga A., Huynh K.T., Pisano M.G., Tripp V.T., Young D.D., Poutsma J.C. Int. J. Mass Spectrom. 2014, 369, 71-80. doi: 10.1016/j.ijms.2014.06.010
- Wang J., Liang Y.-L., Qu J. Chem. Commun. 2009, 5144-5146. doi: 10.1039/b910239f
- Zinelaabidine C., Souad O., Zoubir J., Malika B., Nour-Eddine A. Int. J. Chem. 2012, 4, 73-79. doi: 10.5539/ijc.v4n3p73
- Khelili S., de Tullio P., Lebrun P., Fillet M., Antoine M.-H., Ouedraogo R., Dupont L., Fontaine J., Felekidis A., Leclerc G., Delarge J., Pirotte B. Bioorg. Med. Chem. 1999, 7, 1513-1520. doi: 10.1016/S0968-0896(99)00082-6
- Груздев Д.А., Левит Г.Л., Ольшевская В.А., Краснов В.П. ЖОрХ. 2017, 53, 756-762.
- Gruzdev D.A., Levit G.L., Ol'shevskaya V.A., Krasnov V.P. Russ. J. Org. Chem. 2017, 53, 769-776. doi: 10.1134/S1070428017050190
- Barlos K., Mamos P., Papaioannou D., Patrianakou S. J. Chem. Soc., Chem. Commun. 1987, 1583-1584. doi: 10.1039/C39870001583
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