Suzuki–Miyaura coupling of unstrained ketones via chelation-assisted C–C bond cleavage

2018 ◽  
Vol 16 (39) ◽  
pp. 7174-7177 ◽  
Author(s):  
Cheng Jiang ◽  
Zhao-Jing Zheng ◽  
Tian-Yang Yu ◽  
Hao Wei

Herein, we report that unstrained ketones can be efficiently employed as electrophiles in Suzuki–Miyaura reactions via catalytic activation of unstrained C–C bonds assist by an N-containing directing group.

2021 ◽  
Author(s):  
Yingtao Wu ◽  
Chao Pi ◽  
Yangjie Wu ◽  
Xiuling Cui

In this tutorial review, the rapid advances of directing group (DG) migration in transition-metal-catalysed direct C–H activation was presented through analyzing and comparing the different bond cleavage trigger DG migration (including N–O, N–C, N–N or O–C).


2020 ◽  
Vol 56 (89) ◽  
pp. 13820-13823
Author(s):  
Sen Li ◽  
Kun Jie ◽  
Wenjie Yan ◽  
Qingjun Pan ◽  
Min Zhang ◽  
...  

Herein, copper-catalyzed direct C–C bond cleavage of amides fused to 8-aminoquinoline as a directing group to form urea in the presence of amines and dioxygen is reported.


2019 ◽  
Vol 38 (23) ◽  
pp. 4539-4542
Author(s):  
Julia P. Sarju ◽  
Debashish Dey ◽  
Javier Torroba ◽  
Adrian C. Whitwood ◽  
Kelly Redeker ◽  
...  

2019 ◽  
Author(s):  
Sandeep Pimparkar ◽  
Trisha Bhattacharya ◽  
Arun Maji ◽  
Argha Saha ◽  
Ramasamy Jayarajan ◽  
...  

The significance of site selective functionalization stands upon the superior selectivity, easy synthesis and diverse product utility. In this work we demonstrate the <i>para</i>-selective introduction of versatile nitrile moiety, enabled by detachable and reusable H-bonded auxiliary. The methodology holds its efficiency irrespective of substrate electronic bias. The conspicuous shift in the step energetics was probed by both experimental and computational mechanistic tools heralds the inception of <i>para</i>-deuteration. The synthetic impact of the methodology was highlighted with reusability of directing group and post synthetic modifications


2019 ◽  
Author(s):  
Sandeep Pimparkar ◽  
Trisha Bhattacharya ◽  
Arun Maji ◽  
Argha Saha ◽  
Ramasamy Jayarajan ◽  
...  

The significance of site selective functionalization stands upon the superior selectivity, easy synthesis and diverse product utility. In this work we demonstrate the <i>para</i>-selective introduction of versatile nitrile moiety, enabled by detachable and reusable H-bonded auxiliary. The methodology holds its efficiency irrespective of substrate electronic bias. The conspicuous shift in the step energetics was probed by both experimental and computational mechanistic tools heralds the inception of <i>para</i>-deuteration. The synthetic impact of the methodology was highlighted with reusability of directing group and post synthetic modifications


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