Unusual phosphine oxidation: new triazolopyridyl-quinolyl phosphine oxide fluorescent dyes-Reference-Cited by-同舟云学术

Unusual phosphine oxidation: new triazolopyridyl-quinolyl phosphine oxide fluorescent dyes

Published:2015 Issue:38 Volume:5 Page:29809-29813
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Ballesteros-Garrido R.¹²³⁴⁵,Abarca B.⁶⁷⁸⁹¹⁰,Ballesteros R.⁶⁷⁸⁹¹⁰,Colobert F.¹²³⁴⁵,Leroux F. R.¹²³⁴⁵,García-España E.¹¹⁸¹²¹⁰

Affiliation:

1. Laboratoire de Chimie Moléculaire

2. UMR CNRS 7509

3. Université de Strasbourg (ECPM)

4. 67087 Strasbourg

5. France

6. Departamento de Química Orgánica

7. Facultad de Farmacia

8. Universidad de Valencia

9. 46100 Burjassot

10. Spain

11. ICMol Instituto de Ciencia Molecular

12. Paterna

Abstract

3-(2-Pyridyl)-[1,2,3]triazolo[1,5-a]quinolylphosphines suffer an unusual phosphine oxidation due to their special geometry that allows a σ-donation of the nitrogen (N1) lone pair to phosphorus.

Funder

Generalitat Valenciana

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA04386G

Reference21 articles.

1. B. Abarca and R.Ballesteros-Garrido, Topics in Heterocyclic Chemistry, Chemistry of 1,2,3-triazoles, Springer, Heildelberg, 2014, vol. 40, pp. 325–378

2. G. Jones and B.Abarca, Adv. Heterocyclic Chem., The chemistry of the [1,2,3]triazolo[1,5-a]pyridines: an update, Elsevier, Heildelberg, 2010, vol. 100, pp. 195–252

3. Rhodium-Catalyzed NH Insertion of Pyridyl Carbenes Derived from Pyridotriazoles: A General and Efficient Approach to 2-Picolylamines and Imidazo[1,5-a]pyridines

4. The deprotonative metalation of [1,2,3]triazolo[1,5-a]quinoline. Synthesis of 8-haloquinolin-2-carboxaldehydes

5. Triazolopyridines. Part 2. Preparation of 7-substituted triazolo[1,5a]pyridines by directed lithiation

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