电邮这篇文章 Synthesis of Ethyl Ester of 11-Deoxy-13,14-didehydro-17-methyl-20-norprostaglandin B1_Analog of Misoprostol
- 作者: Ivanova N.A.1, Shavaleeva G.A.1, Spirikhin L.V.1, Miftakhov M.S.1
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隶属关系:
- Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)
- 期: 卷 60, 编号 9 (2024)
- 页面: 967-972
- 栏目: Articles
- URL: https://archivog.com/0514-7492/article/view/681711
- DOI: https://doi.org/10.31857/S0514749224090034
- EDN: https://elibrary.ru/QNXXPI
- ID: 681711
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详细
By 1,2-addition to the keto group ethyl-(5-oxocyclopent-1-enyl)heptenoate lithium acetylenide from 4-hydroxy-4,5-dimethylheptin-1, followed by oxidative isomerization of the resulting adduct with PCC was obtained ethyl ester 11-deoxy-13,14-didehydro-17-methyl-20-nor-prostaglandin B1.
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作者简介
N. Ivanova
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)
编辑信件的主要联系方式.
Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-3101-1285
俄罗斯联邦, prosp. Oktabrya, 71, Ufa, 450054
G. Shavaleeva
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)
Email: gushavaleeva@mail.ru
ORCID iD: 0000-0003-1345-9139
俄罗斯联邦, prosp. Oktabrya, 71, Ufa, 450054
L. Spirikhin
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)
Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-3163-882X
俄罗斯联邦, prosp. Oktabrya, 71, Ufa, 450054
M. Miftakhov
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences (UIC UFRC RAS)
Email: gushavaleeva@mail.ru
ORCID iD: 0000-0002-0269-7484
俄罗斯联邦, prosp. Oktabrya, 71, Ufa, 450054
参考
- Collins P.W., Djuric S.W. Chem. Rev. 1993, 93, 1533–1564. doi: 10.1021/cr00020a007
- Peng H., Chen F-E. Org. Biomol. Chem. 2017, 15, 6281–6301. doi: 10.1039/c7ob01341h
- Collins P.W., Djuric S.W. Chem. Rev. 2003, 93, 1534–1537. doi: 10.1021/cr00020a007
- Bindra J.S., Bindra R. Prostaglandin synthesis. New York: Academic Press. 1977, 187.
- Сапожникова Т.А., Зарудий Ф.С., Габдрахманова С.Ф., Хисамутдинова Р.Ю., Макара Н.С., Иванова Н.А., Мифтахов МС., Батталова M.О. Эксперим. и клин. фармакол. 2017, 80, 35–44. [Sapozhnikova T.A., Zarudii F.S., Gabdrakhmanova S.F., Khisamutdinova R.Yu., Makara N.S., Ivanova N.A., Miftakhov M.S., Battalova M.O. Eksperimental′naya i Klinicheskaya Farmakologiya, 2017, 80, 35–44.] doi: 10.30906/0869-2092-2017-80-8-35-44
- Иванова Н.А., Шайнурова А.М., Мифтахов М.С. Хим.-фарм. ж., 1998, 6, 39–40. [Ivanova N.A., Shainurova A.M., Miftakhov M.S. Pharm. Chem. J. 1998, 32, 325–326.] doi: 10.1007/BF02580520
- Chen S-M.L., Grudzinskas C.V., Dessy F. Prostaglandins. 1979, 17, 707–717. doi: 10.1016/s0090-6980(79)80042-8
- Collins P.W., Dajani E.Z., Driskill D.R., Bruhn M.S., Jung C.J., Pappo R. J. Med. Chem. 1977, 20, 1152–1159. doi: 10.1021/jm00219a008
- Collins P.W., Dajani E.Z., Pappo R., Gasiecki A.F., Bianchi R.G., Woods E.M. J. Med. Chem. 1983, 26, 786–790. doi: 10.1021/jm00360a002
- Terinek M., Kozmik V., Palecek J. Collect. Czech. Chem. Commun., 1997, 62, 1325–1341. doi: 10.1135/cccc19971325
- Harikrishna M., Mohan H.R., Dube P.K., Subbaraju G.V. Synth. Commun. 2009, 39, 2763–2775. doi: 10.1080/00397910802664228
- Иванова Н.А., Шавалеева Г.А., Мифтахов М.С. ЖОрХ. 2020, 56, 472–475. [Ivanova N.A., Shavaleeva G.A., Miftakhov M.S. Russ. J. Org. Chem. 2020, 56, 540–543.] doi: 10.1134/s1070428020030288
- Иванова Н.А., Шавалеева Г.А, Фазлиахметова И.Б., Мифтахов М.С. ЖОрХ. 2020, 56, 631–635. [Ivanova N.A. Shavaleeva G.A., Fazliakhmetova I.B., Miftakhov M.S. Russ. J. Org. Chem. 2020, 56, 708–711.] doi: 10.1134/s1070428020040211
