Ruthenium-catalyzed benzylic substitution of benzyl esters with stabilized carbon nucleophiles

2020 ◽  
Vol 56 (22) ◽  
pp. 3273-3276
Author(s):  
Koki Suzuki ◽  
Hiroaki Tsuji ◽  
Motoi Kawatsura

We have accomplished the ruthenium-catalyzed benzylic substitution of benzyl esters with a stabilized carbon nucleophile.

Synlett ◽  
1991 ◽  
Vol 1991 (09) ◽  
pp. 697-698 ◽  
Author(s):  
Tadakatsu Mandai ◽  
Hiroaki Kunitomi ◽  
Kiyoto Higashi ◽  
Mikio Kawada ◽  
Jiro Tsuji

2019 ◽  
Author(s):  
Leiyang Lv ◽  
Dianhu Zhu ◽  
Zihang Qiu ◽  
Jianbin Li ◽  
Chao-Jun Li

Hydroalkylation of unsaturated hydrocarbons with unstablized carbon nucleophiles is difficult and remains a major challenge. The disclosed examples so far mainly focused on the involvement of heteroatom and/or stabilized carbon nucleophiles as efficient reaction partners. Reported here is an unprecedented regioselective nickel-catalyzed hydroalkylation of 1,3-dienes with hydrazones, generated in situ from abundant aryl aldehydes and ketones and acted as both the sources of unstabilized carbanions and hydride. With this strategy, both terminal and sterically hindered internal dienes are hydroalkylated efficiently in a highly selective manner, thus providing a novel and reliable catalytic method to construct challenging C(sp3)-C(sp3) bonds.


2021 ◽  
Author(s):  
Juliana R. Alexander ◽  
Paul V. Kevorkian ◽  
Joseph J. Topczewski
Keyword(s):  

ChemInform ◽  
2008 ◽  
Vol 39 (12) ◽  
Author(s):  
Catelijne H. M. Amijs ◽  
Veronica Lopez-Carrillo ◽  
Antonio M. Echavarren
Keyword(s):  

2010 ◽  
Vol 51 (15) ◽  
pp. 2032-2035 ◽  
Author(s):  
Puhui Li ◽  
Max M. Majireck ◽  
Jason A. Witek ◽  
Steven M. Weinreb
Keyword(s):  

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