Selective Synthesis of 1-O-Alkyl(poly)glycerol Ethers by Catalytic Reductive Alkylation of Carboxylic Acids with a Recyclable Catalytic System

ChemSusChem ◽  
2012 ◽  
Vol 5 (12) ◽  
pp. 2397-2409 ◽  
Author(s):  
Marc Sutter ◽  
Wissam Dayoub ◽  
Estelle Métay ◽  
Yann Raoul ◽  
Marc Lemaire
2016 ◽  
Vol 52 (24) ◽  
pp. 4509-4512 ◽  
Author(s):  
Basujit Chatterjee ◽  
Chidambaram Gunanathan

A highly efficient catalytic system is reported for chemoselective synthesis of mono-deuterated terminal alkynes using deuterium oxide in which the reaction proceeds via Ru–acetylide intermediates formed by selective activation of the sp-CH bond.


2016 ◽  
Vol 52 (9) ◽  
pp. 1855-1858 ◽  
Author(s):  
Keith G. Andrews ◽  
Declan M. Summers ◽  
Liam J. Donnelly ◽  
Ross M. Denton

We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic acids.


Synthesis ◽  
2012 ◽  
Vol 44 (11) ◽  
pp. 1672-1678 ◽  
Author(s):  
Yoshihiro Kon ◽  
Kazuhiko Sato ◽  
Houjin Hachiya ◽  
Yutaka Ono ◽  
Kiyoshi Takumi ◽  
...  

ChemInform ◽  
2007 ◽  
Vol 38 (41) ◽  
Author(s):  
Sandrine Langle ◽  
Samuel Inack Ngi ◽  
Elsa Anselmi ◽  
Mohamed Abarbri ◽  
Jerome Thibonnet ◽  
...  

2005 ◽  
Vol 83 (6-7) ◽  
pp. 569-573 ◽  
Author(s):  
Nitin T Patil ◽  
Nirmal K Pahadi ◽  
Yoshinori Yamamoto

We have developed a catalytic system that enables the addition of alcohols to allenes using a combination of 5 mol% Pd(PPh3)4 and 10 mol% benzoic acid. Likewise, the addition reaction of carboxylic acids to alkynes is described. In all cases the reaction proceeded well, giving the corresponding allylation products in good-to-high yields with high regio- and stereoselectivities.Key words: addition, alcohols, carboxylic acids, allenes, alkynes, palladium.


2018 ◽  
Vol 57 (36) ◽  
pp. 11673-11677 ◽  
Author(s):  
Weiping Liu ◽  
Basudev Sahoo ◽  
Anke Spannenberg ◽  
Kathrin Junge ◽  
Matthias Beller

2021 ◽  
Author(s):  
Aleksandra Potrząsaj ◽  
Mateusz Musiejuk ◽  
Wojciech Chaładaj ◽  
Maciej Giedyk ◽  
Dorota Gryko

Ring-opening of epoxides furnishing either linear or branched products belongs to the group of classic transformations in organic synthesis. However, the regioselective cross-electrophile coupling of aryl epoxides with aryl halides still represents a key challenge. Herein, we report vitamin B12/Ni dual-catalytic system that allows for the selective synthesis of linear products under blue-light irradiation.


ChemInform ◽  
2006 ◽  
Vol 37 (16) ◽  
Author(s):  
Jose M. Concellon ◽  
Jose Ramon Suarez ◽  
Virginia del Solar ◽  
Ricardo Llavona

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