N-alkyl-2-halo- and 2,2-dihaloaldimines in the Pudovik reaction


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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

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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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