scholarly journals Ni-Electrocatalytic C(sp3)–C(sp3) Doubly Decarboxylative Coupling

Author(s):  
benxiang zhang ◽  
yang gao ◽  
yuta hioki ◽  
martins oderinde ◽  
jennifer qiao ◽  
...  

This work presents a modern spin on one of the oldest known Csp3–Csp3 bond forming reactions in synthetic chemistry: the Kolbe electrolysis. This reaction holds incredible promise for synthesis, yet its use has been near non-existent in mainstream organic synthesis. In contrast to the strongly oxidative electrolytic protocol employed traditionally since the 19th century, the present method utilizes in situ generated redox-active esters (RAEs) which are combined with a mildly reductive Ni-electrocatalytic cycle. It can be used to heterocouple 1o, 2o, and even certain 3o RAEs with a protocol reminiscent of amide bond formation in terms of simplicity. Due to its mild nature the reaction tolerates a range of functional groups, is scalable, and was strategically enlisted for the synthesis of 25 known compounds to reduce overall step-counts by 74%.

2014 ◽  
Vol 11 (4) ◽  
pp. 592-604 ◽  
Author(s):  
Natalia Lukasik ◽  
Ewa Wagner-Wysiecka

CCS Chemistry ◽  
2020 ◽  
pp. 2764-2771
Author(s):  
Bao-Gui Cai ◽  
Shuai-Shuai Luo ◽  
Lin Li ◽  
Lei Li ◽  
Jun Xuan ◽  
...  

2017 ◽  
Vol 15 (30) ◽  
pp. 6426-6432 ◽  
Author(s):  
Daan F. J. Hamstra ◽  
Danny C. Lenstra ◽  
Tjeu J. Koenders ◽  
Floris P. J. T. Rutjes ◽  
Jasmin Mecinović

In situ reduction of phosphine oxide by poly(methylhydrosiloxane) leads to efficient amidation reaction between carboxylic acids and amines.


2021 ◽  
Author(s):  
Jiahua Wang ◽  
Manzar Abbas ◽  
Junyou Wang ◽  
Evan Spruijt

ChemInform ◽  
2015 ◽  
Vol 46 (14) ◽  
pp. no-no
Author(s):  
Natalia Lukasik ◽  
Ewa Wagner-Wysiecka

2016 ◽  
Vol 14 (2) ◽  
pp. 430-433 ◽  
Author(s):  
Maria E. Due-Hansen ◽  
Sunil K. Pandey ◽  
Elisabeth Christiansen ◽  
Rikke Andersen ◽  
Steffen V. F. Hansen ◽  
...  

A protocol for amide coupling by in situ formation of acyl fluorides and reaction with amines at elevated temperature has been developed and found to be efficient for coupling of sterically hindered substrates and electron deficient amines where standard methods failed.


2020 ◽  
Vol 5 (4) ◽  
pp. 645-650 ◽  
Author(s):  
Alejandro Mata ◽  
Ulrich Weigl ◽  
Oliver Flögel ◽  
Pius Baur ◽  
Christopher A. Hone ◽  
...  

Acyl azides were safely generated by using nitrous acid in water and reacted in situ within a flow system. The acyl azide was efficiently extracted into the organic phase containing an amine nucleophile for a highly enantioselective peptide coupling.


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