Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes-Reference-Cited by-同舟云学术

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Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes

Published:2016 Issue:3 Volume:6 Page:882-889
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Szeto Kai C.¹²³⁴⁵,Sahyoun Wissam¹²³⁴⁵,Merle Nicolas¹²³⁴⁵,Castelbou Jessica Llop⁶⁷⁸⁹,Popoff Nicolas¹²³⁴⁵,Lefebvre Frédéric¹²³⁴⁵,Raynaud Jean¹²³⁴⁵,Godard Cyril⁶⁷⁸⁹,Claver Carmen⁶⁷⁸⁹,Delevoye Laurent¹⁰¹¹¹²¹³⁵,Gauvin Régis M.¹⁰¹¹¹²¹³⁵,Taoufik Mostafa¹²³⁴⁵

Affiliation:

1. C2P2, (CNRS-UMR 5265)

2. Université Lyon 1

3. ESCPE Lyon

4. 69626 Villeurbanne Cedex

5. France

6. Department of Physical and Inorganic Chemistry

7. Universitat Rovira I Virgili

8. Tarragona

9. Spain

10. UCCS (CNRS-UMR 8181)

11. Université Lille Nord de France

12. USTL

13. 59652 Villeneuve d'Ascq

Abstract

Supported Lewis acid/base systems based have been prepared and characterized.

Funder

Centre National de la Recherche Scientifique

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CY/C5CY01372K

Reference82 articles.

1. Alkyne metathesis

2. Ring Closing Alkyne Metathesis. Comparative Investigation of Two Different Catalyst Systems and Application to the Stereoselective Synthesis of Olfactory Lactones, Azamacrolides, and the Macrocyclic Perimeter of the Marine Alkaloid Nakadomarin A

3. Total Synthesis of Microtubule-Stabilizing Agent (−)-Laulimalide1

4. Polyene pheromone components from an arctiid moth (Utetheisa ornatrix): characterization and synthesis

5. Stereoselective Synthesis of Z-Alkenes

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