Unusual Stereoselectivity in Elimination Reactions of Allylic Acetate Catalyzed by Pd(PPh3)4 in (±)-9α,11α,15α-triacetate Cloprostenol p-Methoxybenzyl Ester
- 作者: Zagitov V.V.1, Vostrikov N.S.1, Miftakhov M.S.1
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隶属关系:
- Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
- 期: 卷 60, 编号 10 (2024)
- 页面: 1048-1053
- 栏目: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/682487
- DOI: https://doi.org/10.31857/S0514749224100074
- EDN: https://elibrary.ru/QLRUKN
- ID: 682487
如何引用文章
详细
Attempts to replace the allylic C15-acetate group of cloprostenol with a tosyl group under phase-transfer catalysis conditions (СH2Cl2/H2O, R3R′N+Hal-, NaOH, TsOH, Pd(PPh3)4) led to the corresponding 13E, 15Z derivative with moderate yield. The same compound is stereoselectivity formed in high yield when this reaction is carried out in a THF-Pd(PPh3)4-NaH medium.
作者简介
V. Zagitov
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
Email: vostrikov@anrb.ru
俄罗斯联邦, prosp. Oktyabrya, 71, Ufa, 450054
N. Vostrikov
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
编辑信件的主要联系方式.
Email: vostrikov@anrb.ru
prosp. Oktyabrya, 71, Ufa, 450054
M. Miftakhov
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
Email: vostrikov@anrb.ru
俄罗斯联邦, prosp. Oktyabrya, 71, Ufa, 450054
参考
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