scholarly journals Practical Ni-Catalyzed Aryl–Alkyl Cross-Coupling of Secondary Redox-Active Esters

2016 ◽  
Vol 138 (7) ◽  
pp. 2174-2177 ◽  
Author(s):  
Josep Cornella ◽  
Jacob T. Edwards ◽  
Tian Qin ◽  
Shuhei Kawamura ◽  
Jie Wang ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Active Esters ◽  
Redox Active

scholarly journals Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids

2016 ◽  
Vol 55 (33) ◽  
pp. 9676-9679 ◽  
Author(s):  
Jie Wang ◽  
Tian Qin ◽  
Tie-Gen Chen ◽  
Laurin Wimmer ◽  
Jacob T. Edwards ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Boronic Acids ◽  
Active Esters ◽  
Redox Active

Quaternary Centers via Ni-Catalyzed Cross-Coupling of Tertiary Carboxylic Acids and Aryl Zinc Reagents

2018 ◽  
Author(s):  
Phil Baran ◽  
Pavel Mykhailiuk ◽  
haolin zhang ◽  
Rohan R. Merchant ◽  
Courtney A. Smith ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Cross Coupling ◽  
Simple Method ◽  
Quaternary Centers ◽  
Active Esters ◽  
Redox Active ◽  
The Cross

<div> <div> <div> <p>This work bridges a gap in the cross-coupling of aliphatic redox-active esters with aryl zinc reagents. Previously limited to primary, secondary and specialized tertiary centers, a new protocol has been devised to enable the coupling of general tertiary systems using Ni-catalysis. The scope of this operationally simple method is broad and can be used to simplify the synthesis of medicinally relevant motifs bearing quaternary centers. </p> </div> </div> </div>

Visible-light-induced iodine anion catalyzed decarboxylative/ deaminative C-H alkylation of enamides

2021 ◽  
Author(s):  
Jia-Xin Wang ◽  
Ya-Ting Wang ◽  
Hao Zhang ◽  
Ming-Chen Fu
Keyword(s):  
Amino Acid ◽  
Visible Light ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Active Esters ◽  
Cross Coupling Reactions ◽  
Redox Active ◽  
Iodine Anion

A visible-light-induced iodine anion catalyzed C-H stereoselective alkylation of enamides has been developed. Redox-active esters and Katritzky salts of the amino acid are amenable for decarboxylative/deaminative cross-coupling reactions, delivering various...

ChemInform Abstract: A General Alkyl-Alkyl Cross-Coupling Enabled by Redox-Active Esters and Alkylzinc Reagents.

ChemInform ◽  
2016 ◽  
Vol 47 (42) ◽  
Author(s):  
Tian Qin ◽  
Josep Cornella ◽  
Chao Li ◽  
Lara R. Malins ◽  
Jacob T. Edwards ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Active Esters ◽  
Redox Active

scholarly journals Active template rotaxane synthesis through the Ni-catalyzed cross-coupling of alkylzinc reagents with redox-active esters

2019 ◽  
Vol 10 (30) ◽  
pp. 7269-7273 ◽  
Author(s):  
Javier Echavarren ◽  
Malcolm A. Y. Gall ◽  
Adrian Haertsch ◽  
David A. Leigh ◽  
Vanesa Marcos ◽  
...  
Keyword(s):  
Template Synthesis ◽  
Cross Coupling ◽  
Active Esters ◽  
Redox Active ◽  
Organozinc Reagents

The Ni-catalyzed C(sp3)–C(sp3) cross-coupling of redox-active esters and organozinc reagents is used for the active template synthesis of ‘impossible’ rotaxanes.

Quaternary Centers via Ni-Catalyzed Cross-Coupling of Tertiary Carboxylic Acids and Aryl Zinc Reagents

2018 ◽  
Author(s):  
Phil Baran ◽  
Pavel Mykhailiuk ◽  
haolin zhang ◽  
Rohan R. Merchant ◽  
Courtney A. Smith ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Cross Coupling ◽  
Simple Method ◽  
Quaternary Centers ◽  
Active Esters ◽  
Redox Active ◽  
The Cross

<div> <div> <div> <p>This work bridges a gap in the cross-coupling of aliphatic redox-active esters with aryl zinc reagents. Previously limited to primary, secondary and specialized tertiary centers, a new protocol has been devised to enable the coupling of general tertiary systems using Ni-catalysis. The scope of this operationally simple method is broad and can be used to simplify the synthesis of medicinally relevant motifs bearing quaternary centers. </p> </div> </div> </div>

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