Regioselective ring expansion followed by H-shift of 3-ylidene oxindoles: a convenient synthesis of N-substituted/un-substituted pyrrolo[2,3-c] quinolines and marinoquinolines-Reference-Cited by-同舟云学术

Regioselective ring expansion followed by H-shift of 3-ylidene oxindoles: a convenient synthesis of N-substituted/un-substituted pyrrolo[2,3-c] quinolines and marinoquinolines

Published:2019 Issue:60 Volume:9 Page:35068-35072
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Ramu Gopathi¹²³⁴⁵,Ambala Srinivas¹²³⁴,Nanubolu Jagadeesh Babu¹²³⁴⁶,Nagendra Babu Bathini¹²³⁴⁵^ORCID

Affiliation:

1. Department of Fluoro-Agrochemicals

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad 500 007

4. India

5. Academy of Scientific and Innovative Research (AcSIR)

6. Centre for X-ray Crystallography

Abstract

Herein, we report a simple and metal-free protocol for the synthesis of 4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinolines.

Funder

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA07831B

Reference26 articles.

1. The Synthesis of Thalmicrinone, a Confirmation of Structure

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3. β-Phenylethylamines and the isoquinoline alkaloids

4. Substituted quinolines induce inhibition of proliferation of HTLV-1 infected cells

5. Quinoline: A promising antitubercular target

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