Tandem intramolecular cyclisation/1,3-aryl shift in N-(4,4-diethoxybutyl)-1-arylmethanimines (Kazan reaction): synthesis of 3-benzylidene-1-pyrrolines-Reference-Cited by-同舟云学术

Tandem intramolecular cyclisation/1,3-aryl shift in N-(4,4-diethoxybutyl)-1-arylmethanimines (Kazan reaction): synthesis of 3-benzylidene-1-pyrrolines

Published:2017 Issue:80 Volume:7 Page:50955-50960
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Smolobochkin A. V.¹²³⁴⁵,Gazizov A. S.¹²³⁴⁵^ORCID,Melyashova A. S.¹²³⁴⁵,Voronina J. K.¹²³⁴⁵,Strelnik A. G.¹²³⁴⁵,Vatsadze S. Z.⁶⁷⁸⁵^ORCID,Burilov A. R.¹²³⁴⁵,Pudovik M. A.¹²³⁴⁵,Fedorova O. A.⁹³⁸⁵^ORCID,Sinyashin O. G.¹²³⁴⁵

Affiliation:

1. A.E. Arbuzov Institute of Organic and Physical Chemistry

2. Kazan Scientific Center

3. Russian Academy of Sciences

4. Kazan

5. Russian Federation

6. Lomonosov Moscow State University

7. Chemistry Department

8. Moscow

9. A.N. Nesmeyanov Institute of Organoelement Compounds

Abstract

A novel tandem reaction, which transforms N-(4,4-diethoxybutyl)imines to 3-arylidene-1-pyrrolines via intramolecular Mannich reaction/[1,3]-sigmatropic rearrangement of the aryl fragment is described.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA11216E

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