Аннотация:
The first synthesis of 7-prenylisatin, an isatin-type antibiotic with prominent activity against Bacillus subtilis, has been accomplished in 16% overall yield from 2-methylbut-3-en-2-ol and aniline via a five-step procedure. The protocol includes the aromatic aza-Claisen rearrangement and the Sandmeyer isonitrosoacetanilide isatin synthesis as key steps.
Образец цитирования:
D. Liang, Yu. Wang, “The first synthesis of 7-prenylisatin”, Mendeleev Commun., 29:2 (2019), 172–173
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1460
https://www.mathnet.ru/rus/mendc/v29/i2/p172
Эта публикация цитируется в следующих 2 статьяx:
Gui-Min Liu, Lin-Lin Yuan, Li-Li Zhang, Hong Zeng, “Streptomyces blattellae, a novel actinomycete isolated from the in vivo of a Blattella germanica”, Antonie van Leeuwenhoek, 115:1 (2022), 79
S. G. Zlotin, O. A. Banina, D. V. Sudarikov, A. A. Nigmatov, L. L. Frolova, A. V. Kutchin, “Asymmetric aldol reaction of isatins with acetone in the presence of terpene amino alcohols”, Mendeleev Commun., 30:2 (2020), 147–149
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