One pot synthesis of phenanthridines using a palladium-catalyzed cyclization of aromatic ketoximes with aryl iodides via Beckmann rearrangement-Reference-Cited by-同舟云学术

One pot synthesis of phenanthridines using a palladium-catalyzed cyclization of aromatic ketoximes with aryl iodides via Beckmann rearrangement

Published:2016 Issue:51 Volume:6 Page:45036-45040
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Raju Gajula¹²³⁴⁵,Guguloth Vijayacharan¹²³⁴⁵,Satyanarayana Battu¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. University College of Science

3. Osmania University

4. Hyderabad

5. India 500 007

Abstract

The catalytic reaction of ketoximes with aryl iodides via a Beckmann rearrangement in the presence of a catalytic amount of Pd(OAc)₂, Ag₂O and ZnBr₂ gave substituted phenanthridines in good to excellent yield.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA07423E

Reference50 articles.

1. A review of the chemistry of the antitumor benzo[c]phenanthridine alkaloids nitidine and fagaronine and of the related antitumor alkaloid coralyne

2. Acridine Derivatives as Chemotherapeutic Agents

3. Benzo[c]phenanthridine bases and their antituberculosis activity

4. Ethidium DNA agarose gel electrophoresis: How it started

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