Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones-Reference-Cited by-同舟云学术

Base-mediated regiospecific cascade synthesis of N-(2-pyridyl)pyrroles from N-propargylic β-enaminones

Published:2016 Issue:54 Volume:6 Page:48905-48909
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Shen Jinhai¹²³⁴⁵,Yang Xifa¹²³⁴⁵,Wang Fuyuan¹²³⁴⁵,Wang Yue⁶⁷⁸⁹,Cheng Guolin¹²³⁴⁵,Cui Xiuling¹²³⁴⁵

Affiliation:

1. Key Laboratory of Xiamen Marine and Gene Drugs

2. Institutes of Molecular Medicine and School of Biomedical Sciences

3. Huaqiao University & Engineering Research Center of Molecular Medicine

4. Ministry of Education

5. Xiamen 361021

6. Department of Chemistry

7. SUNY Stony Brook

8. NY 11794-3400

9. USA

Abstract

Two birds with one stone: two classical heterocycles, pyrrole and pyridine, were simultaneously installed from one acyclic enaminone precursor for the preparation of N-(2-pyridyl)pyrroles.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA08987A

Reference60 articles.

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