Ruthenium-catalyzed cyclization of N-carbamoyl indolines with alkynes: an efficient route to pyrroloquinolinones-Reference-Cited by-同舟云学术

Ruthenium-catalyzed cyclization of N-carbamoyl indolines with alkynes: an efficient route to pyrroloquinolinones

Published:2015 Issue:35 Volume:13 Page:9276-9284
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Manoharan Ramasamy¹²³⁴,Jeganmohan Masilamani¹²³⁴

Affiliation:

1. Department of Chemistry

2. Indian Institution of Science Education and Research

3. Pune 411021

4. India

Abstract

A regioselective synthesis of substituted pyrroloquinolinones by a ruthenium-catalyzed oxidative cyclization of substituted N-carbamoyl indolines with alkynes is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01146A

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1. Fine-Tuning the Selectivity of Aldosterone Synthase Inhibitors: Structure−Activity and Structure−Selectivity Insights from Studies of Heteroaryl Substituted 1,2,5,6-Tetrahydropyrrolo[3,2,1-ij]quinolin-4-one Derivatives

2. Development of an Efficient Synthesis of the Pyrrolquinolone PHA-529311

3. A DCM-Type Red-Fluorescent Dopant for High-Performance Organic Electroluminescent Devices

4. Pyrrolo[3,2,1- ij ]quinoline derivatives, a 5-HT 2c receptor agonist with selectivity over the 5-HT 2a receptor: potential therapeutic applications for epilepsy and obesity

5. Synthesis, Structure-Activity Relationships, and Pharmacological Evaluation of Pyrrolo[3,2,1-ij]quinoline Derivatives: Potent Histamine and Platelet Activating Factor Antagonism and 5-Lipoxygenase Inhibitory Properties. Potential Therapeutic Application in Asthma

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