Synthesis of glycyl-(S)-5-hydroxynorvaline
- Авторлар: Chulakov E.N.1, Tumashov A.A.1, Gruzdev D.A.1, Levit G.L.1, Krasnov V.P.1
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Мекемелер:
- Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences
- Шығарылым: Том 59, № 11 (2023)
- Беттер: 1507-1512
- Бөлім: Articles
- URL: https://modernonco.orscience.ru/0514-7492/article/view/667147
- DOI: https://doi.org/10.31857/S0514749223110149
- EDN: https://elibrary.ru/NDGSMP
- ID: 667147
Дәйексөз келтіру
Аннотация
The dipeptide glycyl-( S )-5-hydroxynorvaline was obtained from 1- tert -butyl 5-methyl N -Boc-glycyl-( S )-glutamate as a result of saponification and subsequent reduction of the activated 5-carboxyl group with sodium borohydride followed by removal of the N -Boc and OBu t protecting groups by refluxing in a dioxane-water mixture. Using the example of the synthesis of ( S )-5-hydroxynorvaline, it has been shown that the used sequence of chemical transformations is not accompanied by racemization.
Негізгі сөздер
Авторлар туралы
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
Әдебиет тізімі
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