N-alkyl-2-halo- and 2,2-dihaloaldimines in the Pudovik reaction
- 作者: Gazizov M.B.1, Khairullin R.A.1, Perina A.I.1, Minnikhanova A.A.1, Aksenov N.G.1, Gnezdilov O.I.1, Il’yasov A.V.1, Khayarov K.R.1
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隶属关系:
- Kazan Research Institute of Technology
- 期: 卷 86, 编号 3 (2016)
- 页面: 499-507
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-3632/article/view/214140
- DOI: https://doi.org/10.1134/S1070363216030014
- ID: 214140
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详细
The use of N-alkyl-2-haloaldimines in the imine version of the Pudovik reaction, namely, in the reaction of imines with acid esters of phosphorus acids, much extended the synthetic potential of this reaction due to the fact that the primary addition and protonation product, having quite a mobile single hylogen atom, can undergo both spontaneous transformations and transformations involving other reagents. The reduction of the С–Hlg bond in N-alkyl-2-halo- and -2,2-dihaloaldiminium salts with О,О-dialkyl phosphorodithioic acids was observed for the first time.
作者简介
M. Gazizov
Kazan Research Institute of Technology
编辑信件的主要联系方式.
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
R. Khairullin
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
A. Perina
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
A. Minnikhanova
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
N. Aksenov
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
O. Gnezdilov
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
A. Il’yasov
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
Kh. Khayarov
Kazan Research Institute of Technology
Email: mukattisg@mail.ru
俄罗斯联邦, ul. Karla Marksa 68, Kazan, Tatarstan, 420015
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