Мақаланы E-mail арқылы жіберу Synthesis of Analogue of Bistetrahydroisoquinoline Alkaloids Based on N-Homoveratrylmaleimide
- Авторлар: Remezova G.V.1, Sakhautdinova G.F.1, Sakhautdinov I.M.1
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Мекемелер:
- Ufa Institute of Chemistry – Separate Structural Division of the Federal State Budgetary Scientific Institution “Ufa Federal Research Center of the Russian Academy of Sciences”
- Шығарылым: Том 60, № 9 (2024)
- Беттер: 997-1000
- Бөлім: Articles
- URL: https://gynecology.orscience.ru/0514-7492/article/view/681715
- DOI: https://doi.org/10.31857/S0514749224090077
- EDN: https://elibrary.ru/QNMATW
- ID: 681715
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Аннотация
A new method for the synthesis of a bisbenzylisoquinoline base with a diphenyl oxide fragment based on phosphorane obtained from N-homoveratrylmaleimide is proposed.
Негізгі сөздер
Толық мәтін
Авторлар туралы
G. Remezova
Ufa Institute of Chemistry – Separate Structural Division of the Federal State Budgetary Scientific Institution “Ufa Federal Research Center of the Russian Academy of Sciences”
Хат алмасуға жауапты Автор.
Email: ioh039@mail.ru
ORCID iD: 0009-0003-7525-7943
Ресей, Oktyabrya Ave., 69, Ufa, 450054
G. Sakhautdinova
Ufa Institute of Chemistry – Separate Structural Division of the Federal State Budgetary Scientific Institution “Ufa Federal Research Center of the Russian Academy of Sciences”
Email: ioh039@mail.ru
ORCID iD: 0000-0002-7882-3360
Ресей, Oktyabrya Ave., 69, Ufa, 450054
I. Sakhautdinov
Ufa Institute of Chemistry – Separate Structural Division of the Federal State Budgetary Scientific Institution “Ufa Federal Research Center of the Russian Academy of Sciences”
Email: ioh039@mail.ru
ORCID iD: 0000-0002-0041-8779
Ресей, Oktyabrya Ave., 69, Ufa, 450054
Әдебиет тізімі
- Weber C., Opatz T. Alkaloids: Chem. Biol. 2019, 81, 1–114. doi: 10.1016/bs.alkal.2018.07.001
- Sakhautdinova G.F., Sakhautdinov I.M., Nazarov I.S., Mustafin A.G., Vinogradova V.I., Yunusov M. S. Chemistry of Natural Compounds. 2022, 58, 903–907. doi: 10.1007/s10600-022-03825-4
- Сахаутдинов И.М., Маликова Р.Н., Сахаутдинова Г.Ф., Абдуллин М.Ф., Нугуманов Т.Р., Мустафин А.Г. ЖОрХ. 2022, 58, 1387–1392. doi: 10.31857/S0514749222120072 [Sakhautdinov I. M., Malikova R. N., Sakhautdinova G. F., Abdullin M.F., Nugumanov T.R., Mustafin A.G. Russ. J. Org. Chem. 2022, 58, 1984–1988.] doi: 10.1134/S1070428022120302
- Liu G.N., Luo R.H., Zhang X.J., Y. Zhou, J. Li, Zheng Y.T., Liu H. Med. Chem. 2014, 4, 573. doi: 10.4172/2161-0444.1000196
- Xu W.L., Tang L., Ge C.Y., Chen J., Zhoua L. Adv. Synth.Catal. 2019, 361, 2268. doi: 10.1002/adsc.201801436
- Sakhautdinova G.F., Sakhautdinov I.M., Mendeleev Commun. 2024, 34, 272–273. doi: 10.1016/j.mencom.2024.02.036
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