scholarly journals Exploiting single-electron transfer in Lewis pairs for catalytic bond-forming reactions

2020 ◽  
Vol 11 (17) ◽  
pp. 4305-4311 ◽  
Author(s):  
Yoshitaka Aramaki ◽  
Naoki Imaizumi ◽  
Mao Hotta ◽  
Jun Kumagai ◽  
Takashi Ooi

Radical–ion pair generation from common Lewis pairs and its application to catalytic carbon–carbon bond formation.

RSC Advances ◽  
2015 ◽  
Vol 5 (22) ◽  
pp. 16801-16814 ◽  
Author(s):  
Zhi Guan ◽  
Ling-Yu Li ◽  
Yan-Hong He

This article reviews the hydrolase-catalyzed asymmetric carbon–carbon bond-forming reactions for the preparation of enantiomerically enriched compounds in organic synthesis.


2018 ◽  
Vol 42 (9) ◽  
pp. 481-485
Author(s):  
Xiulian Zhang ◽  
Zhicheng Zhang ◽  
Yongbin Xie ◽  
Yujie Jiang ◽  
Ruibo Xu ◽  
...  

A simple and efficient access to arylboronates was achieved with methanol-initiated borylation of aryldiazonium salts. Reduction of aryldiazonium ions by single electron transfer from methanol affords aryl radical species, which undergo a subsequent C–B bond formation with bis(pinacolato)diboron. This highly practical borylation process, which can be carried out on the gram-scale, enjoys operational simplicity as well as mild and catalyst-free conditions.


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