A mild and efficient method for the synthesis of a new optically active diallyl selenide and its catalytic activity in the allylic chlorination of natural terpenes-Reference-Cited by-同舟云学术

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A mild and efficient method for the synthesis of a new optically active diallyl selenide and its catalytic activity in the allylic chlorination of natural terpenes

Published:2016 Issue:4 Volume:40 Page:3395-3399
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Boualy Brahim¹²³⁴⁵,El Houssame Soufiane¹²³⁴⁵,Sancineto Luca⁶⁷⁸⁹¹⁰,Santi Claudio⁶⁷⁸⁹¹⁰,Ait Ali Mustapha¹¹¹²¹³¹⁴¹⁵,Stoeckli-Evans Helen¹⁶¹⁷¹⁸¹⁹,El Firdoussi Larbi¹¹¹²¹³¹⁴¹⁵

Affiliation:

1. Laboratoire de Chimie et Modélisation Mathématique

2. Université Hassan 1er

3. Faculté Polydisciplinaire de Khouribga

4. 25000 Khouribga

5. Morocco

6. Department of Pharmaceutical Sciences

7. Group of Catalysis and Organic Green Chemistry

8. University of Perugia

9. 06100 Perugia

10. Italy

11. Equipe de Chimie de Coordination et Catalyse

12. Département de Chimie

13. Université Cadi Ayyad

14. Faculté des Sciences Semlalia

15. 40001 Marrakech

16. Institute of Physics

17. University of Neuchâtel

18. CH-2000 Neuchâtel

19. Switzerland

Abstract

An organoselenide compound was synthesized starting from β-pinene. The activity of this complex towards allylic chlorination has been studied.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/NJ/C5NJ02797G

Reference29 articles.

1. Topics in Current Chemistry, in Organoselenium Chemistry: Modern Developments in Organic Synthesis, ed. T. Wirth, Springer, Germany, 2000

2. Comprehensive Organometallic Chemistry-III, Selenium, ed. T. Wirth and R. H. Crabtree and D. M. P. Mingos, Pergamon Press, 2007, ch. 9

3. T. Wirth , Organoselenium Chemistry, Springer-Verlag, Berlin, 2000, vol. 208

4. Recent developments in the chemistry of selenoethers and telluroethers

5. Chemistry of selena macrocycles

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