Synthesis and reactions of allylic azides of the adamantane series
- Авторлар: Leonova M.1, Baimuratov M.1, Klimochkin Y.1
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Мекемелер:
- Samara State Technical University
- Шығарылым: Том 59, № 11 (2023)
- Беттер: 1455-1464
- Бөлім: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/247257
- DOI: https://doi.org/10.31857/S0514749223110071
- EDN: https://elibrary.ru/NDPWNK
- ID: 247257
Дәйексөз келтіру
Аннотация
A mixture of nucleophilic substitution product and isomeric azide resulting from [3,3]-sigmatropic rearrangement was obtained by interaction of allyl bromides of adamantane series with sodium azide. Epoxidation reactions of allylic azides of the adamantane series were investigated. The reduction of the obtained trans -2-(adamantan-1-yl)-3-(azidomethyl)oxirane with lithium alumohydride synthesized ( S *)-(adamantan-1-yl)[( S *)-aziridin-2-yl]methanol which, when heated with hydrochloric acid, gives the product of the aziridine ring opening is (1 S *,2 R *)-1-(adamantan-1-yl)-3-chloro-1-hydroxypropan-2-amino chloride.
Негізгі сөздер
Авторлар туралы
M. Leonova
Samara State Technical University
Email: mvleon@mail.ru
M. Baimuratov
Samara State Technical University
Yu. Klimochkin
Samara State Technical University
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