Issue 21, 2011
From the journal:

Organic & Biomolecular Chemistry

Click-chemistry approach to isoxazole-containing α-CF3-substituted α-aminocarboxylates and α-aminophosphonates

Daria V. Vorobyeva,*a   Natalya M. Karimova,a   Irina L. Odinets,a   Gerd-Volker Röschenthaler*b  and  Sergey N. Osipova  

* Corresponding authors

a A.N. Nesmeyanov Institute of Organoelement compounds, Russian Academy of Sciences, Russia. Vavilov str. 28, Moscow, Russia
E-mail: vorobyeva-daria@yandex.ru
Fax: +7 495 135 5085

b Jacobs University Bremen gGmbH, P.O. Box 750 561, D-28725, Bremen, Germany
E-mail: g.roeschenthaler@jacobs-university.de

Abstract

A convenient strategy for the synthesis of isoxazole-containing α-CF3-substituted α-aminocarboxylates and α-aminophosphonates have been developed. The method is based on copper-catalyzed 1,3-dipolar cycloaddition of different aromatic nitrile oxides to functionalized acetylenes.

Graphical abstract: Click-chemistry approach to isoxazole-containing α-CF3-substituted α-aminocarboxylates and α-aminophosphonates

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C1OB06040F
Article type
Paper
Submitted
28 Jun 2011
Accepted
29 Jul 2011
First published
01 Aug 2011

Org. Biomol. Chem., 2011,9, 7335-7342

Permissions

Request permissions

Click-chemistry approach to isoxazole-containing α-CF3-substituted α-aminocarboxylates and α-aminophosphonates

D. V. Vorobyeva, N. M. Karimova, I. L. Odinets, G. Röschenthaler and S. N. Osipov, Org. Biomol. Chem., 2011, 9, 7335 DOI: 10.1039/C1OB06040F

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