ChemInform Abstract: Transition-Metal-Free α-Arylation of Enolizable Aryl Ketones and Mechanistic Evidence for a Radical Process.

ChemInform ◽  
2016 ◽  
Vol 47 (4) ◽  
pp. no-no
Author(s):  
Martin Pichette Drapeau ◽  
Indira Fabre ◽  
Laurence Grimaud ◽  
Ilaria Ciofini ◽  
Thierry Ollevier ◽  
...  
2015 ◽  
Vol 127 (36) ◽  
pp. 10733-10737 ◽  
Author(s):  
Martin Pichette Drapeau ◽  
Indira Fabre ◽  
Laurence Grimaud ◽  
Ilaria Ciofini ◽  
Thierry Ollevier ◽  
...  

2015 ◽  
Vol 54 (36) ◽  
pp. 10587-10591 ◽  
Author(s):  
Martin Pichette Drapeau ◽  
Indira Fabre ◽  
Laurence Grimaud ◽  
Ilaria Ciofini ◽  
Thierry Ollevier ◽  
...  

2020 ◽  
Vol 7 (17) ◽  
pp. 2480-2485 ◽  
Author(s):  
Wei-Hua Huang ◽  
Gong-Bin Huang ◽  
Wen-Run Zhu ◽  
Jiang Weng ◽  
Gui Lu

α-Arylated ketones were accessed via oxyallyl cation capture with arylboronic acids in good yields with broad substrate tolerance.


2019 ◽  
Vol 17 (10) ◽  
pp. 2725-2733 ◽  
Author(s):  
Yang Yuan ◽  
Hailu Tan ◽  
Lingkai Kong ◽  
Zhong Zheng ◽  
Murong Xu ◽  
...  

Atom-economical synthesis of tetrasubstituted furans from α-aryl ketones and alkynones through base-promoted cleavage of unstrained C–C single bonds of ketones and subsequent Zn-catalyzed cyclization.


2021 ◽  
Vol 17 ◽  
pp. 551-557
Author(s):  
Xiaojuan Li ◽  
Qiang Zhang ◽  
Weigang Zhang ◽  
Jinzhu Ma ◽  
Yi Wang ◽  
...  

The difunctionalization of alkenes involving a trifluoromethylthio group (SCF3) for the conversion of versatile and readily available olefins into structurally more complex molecules has been successfully studied. However, the disproportionate dithiolation of alkenes is unknown. Herein, a transition-metal-free protocol is presented for the vicinal trifluoromethylthio–thiolation of unactivated alkenes via a radical process under mild conditions with a broad substrate scope and excellent tolerance.


Synlett ◽  
2021 ◽  
Author(s):  
Li Sun ◽  
Yicheng Zhang ◽  
jie liu ◽  
Pinhua Li

A transition-metal-free visible-light photoredox-catalyzed decarboxylative alkylation of benzylic C-(sp3)−H bonds of N-aryl tetrahydroisoquinolines is reported. The developed methodology tolerates various functional groups and proceeds smoothly without the requirement of stoichiometric oxidants. A preliminary mechanistic study indicated that a radical process is involved in the reaction.


2015 ◽  
Vol 13 (6) ◽  
pp. 1592-1599 ◽  
Author(s):  
Gang Liu ◽  
Congbin Fan ◽  
Jie Wu

Recent advances in the insertion of sulfur dioxide under transition metal catalysis or metal-free conditions via a radical process are presented.


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