Issue 15, 2016
From the journal:

RSC Advances

Synthesis of novel fluorescent 12a-aryl substituted indoxylisoquinolines via aryne-induced domino process†

A. V. Varlamov,a   N. I. Guranova,a   R. A. Novikov,b   V. V. Ilyushenkova,a   V. N. Khrustalev,a   N. S. Baleeva,c   T. N. Borisovaa  and  L. G. Voskressensky*a  

* Corresponding authors

a Organic Chemistry Department, Peoples' Friendship University of Russia, 6, Miklukho-Maklaya St., Moscow 117198, Russia
E-mail: lvoskressensky@sci.pfu.edu.ru

b N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47, Leninskij avenue, Moscow 119991, Russia

c Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10, Miklukho-Maklaya St, Moscow 117997, Russia

Abstract

A novel effective protocol towards indolo[2,1-a]isoquinolinones via aryne-induced migration of aryl-anion in aryloxy substituted 3,4-dihydroisoquinolines is reported. These novel 12a-aryl substituted indoxylisoquinolines exhibit fluorescence properties and are characterized by green-shifted spectra and moderate quantum yields.

Graphical abstract: Synthesis of novel fluorescent 12a-aryl substituted indoxylisoquinolines via aryne-induced domino process

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5RA25323C
Article type
Communication
Submitted
05 ⴷⵓⵊ 2015
Accepted
20 ⵉⵏⵏ 2016
First published
22 ⵉⵏⵏ 2016

RSC Adv., 2016,6, 12642-12646

Permissions

Request permissions

Synthesis of novel fluorescent 12a-aryl substituted indoxylisoquinolines via aryne-induced domino process

A. V. Varlamov, N. I. Guranova, R. A. Novikov, V. V. Ilyushenkova, V. N. Khrustalev, N. S. Baleeva, T. N. Borisova and L. G. Voskressensky, RSC Adv., 2016, 6, 12642 DOI: 10.1039/C5RA25323C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements