Mono- and Dialkylations of Pyrrole at C2 and C5 Positions by Nucleophilic Substitution Reaction in Ionic Liquid-Reference-Cited by-同舟云学术

Mono- and Dialkylations of Pyrrole at C2 and C5 Positions by Nucleophilic Substitution Reaction in Ionic Liquid

Published:2005-03-01 Issue:7 Volume:7 Page:1231-1234
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Jorapur Yogesh R.¹,Lee Chang-Hee¹,Chi Dae Yoon¹

Affiliation:

1. Department of Chemistry, Inha University, 253 Yonghyundong Namgu, Inchon, 402-751 Korea, and Department of Chemistry, Kangwon National University, Chunchon, Kangwon, 200-701 Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol047446v

Reference29 articles.

1. (a) Joule, J. A.; Mills, K.; Smith, G. F. InHeterocyclic Chemistry, 3rd ed.; Chapman & Hall: London, 1995; pp 231−238.

2. Hetero-Aromatic Nitrogen Compounds

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