Issue 9, 2011
From the journal:

RSC Advances

Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids†

Denis S. Baranov,a   Sergei F. Vasilevsky,*a   Brian Goldb  and  Igor V. Alabugin*b  

* Corresponding authors

a Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Science, Novosibirsk, Russian Federation
E-mail: vasilev@ns.kinetics.nsc.ru
Fax: +7(383)3307350

b Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida, USA.
E-mail: alabugin@chem.fsu.edu

Abstract

Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10-anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones – substituted analogues of Aporphinoid alkaloids.

Graphical abstract: Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1RA00622C
Article type
Paper
Submitted
22 Aug 2011
Accepted
08 Sep 2011
First published
25 Oct 2011

RSC Adv., 2011,1, 1745-1750

Permissions

Request permissions

Urea as an organic solvent and reagent for the addition/cyclization/fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids

D. S. Baranov, S. F. Vasilevsky, B. Gold and I. V. Alabugin, RSC Adv., 2011, 1, 1745 DOI: 10.1039/C1RA00622C

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