Enantioselective Construction of Quaternary All-Carbon Centers via Copper-Catalyzed Arylation of Tertiary Carbon-Centered Radicals

2019 ◽  
Vol 141 (5) ◽  
pp. 1887-1892 ◽  
Author(s):  
Lianqian Wu ◽  
Fei Wang ◽  
Pinhong Chen ◽  
Guosheng Liu
ChemInform ◽  
2004 ◽  
Vol 35 (7) ◽  
Author(s):  
Jun'ichi Uenishi ◽  
Motoi Kawatsura ◽  
Daiji Ikeda ◽  
Nobuhiro Muraoka

2020 ◽  
Author(s):  
Haijian Yang ◽  
Dong Xing

<p>Herein, we report a highly diastereo- and enantioselective allylic alkylation of oxozolones with 1,3-dienes by palladium-hydride catalyst under base-free conditions. With DTBM-SEGPHOS as the chiral ligand, a series of enantioenriched oxazolones bearing tertiary carbon centers were synthesized from substituted 1,3-dienes via exclusive 1,2-addition with moderate to good diastereoselectivities and high enantioselectivities. When simple 1,3-butadiene was used as the allyl precursor under this base-free catalytic system, 1,4-addition products were obtained in good yields with high regioselectivities. </p>


2006 ◽  
Vol 4 (9) ◽  
pp. 1806 ◽  
Author(s):  
Jeremy P. Scott ◽  
Peter R. Mullens ◽  
Sarah E. Brewer ◽  
Karel M. J. Brands ◽  
Jennifer R. Chilenski ◽  
...  

2003 ◽  
Vol 2003 (20) ◽  
pp. 3909-3912 ◽  
Author(s):  
Jun′ichi Uenishi ◽  
Motoi Kawatsura ◽  
Daiji Ikeda ◽  
Nobuhiro Muraoka

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