Strongly Entangled Triplet Acyl–Alkyl Radical Pairs in Crystals of Photostable Diphenylmethyl Adamantyl Ketones

Author(s):  
Jin H. Park ◽  
Vince M. Hipwell ◽  
Edris A. Rivera ◽  
Miguel A. Garcia-Garibay
Keyword(s):  
1989 ◽  
Vol 93 (4) ◽  
pp. 1666-1670 ◽  
Author(s):  
H. L. Casal ◽  
D. Griller ◽  
R. J. Kolt ◽  
F. W. Hartstock ◽  
D. M. Northcott ◽  
...  
Keyword(s):  

1997 ◽  
Vol 26 (5) ◽  
pp. 435-436 ◽  
Author(s):  
Yoshihisa Fujiwara ◽  
Kohji Yoda ◽  
Takeshi Aoki ◽  
Yoshifumi Tanimoto

1970 ◽  
Vol 92 (17) ◽  
pp. 5175-5186 ◽  
Author(s):  
Roger A. Sheldon ◽  
Jay K. Kochi
Keyword(s):  

2019 ◽  
Author(s):  
Tuhin Patra ◽  
Satobhisha Mukherjee ◽  
Jiajia Ma ◽  
Felix Strieth-Kalthoff ◽  
Frank Glorius

<sub>A general strategy to access both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters has been developed. An energy transfer mediated homolysis of unsymmetrical sigma-bonds for a concerted fragmentation/decarboxylation process is involved. As a result, an independent aryl/alkyl radical generation step enables a series of key C-X and C-C bond forming reactions by simply changing the radical trapping agent.</sub>


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Chia-Yu Huang ◽  
Jianbin Li ◽  
Chao-Jun Li

AbstractHydrogen atom abstraction (HAT) from C(sp3)–H bonds of naturally abundant alkanes for alkyl radical generation represents a promising yet underexplored strategy in the alkylation reaction designs since involving stoichiometric oxidants, excessive alkane loading, and limited scope are common drawbacks. Here we report a photo-induced and chemical oxidant-free cross-dehydrogenative coupling (CDC) between alkanes and heteroarenes using catalytic chloride and cobalt catalyst. Couplings of strong C(sp3)–H bond-containing substrates and complex heteroarenes, have been achieved with satisfactory yields. This dual catalytic platform features the in situ engendered chlorine radical for alkyl radical generation and exploits the cobaloxime catalyst to enable the hydrogen evolution for catalytic turnover. The practical value of this protocol was demonstrated by the gram-scale synthesis of alkylated heteroarene with merely 3 equiv. alkane loading.


2021 ◽  
Vol 133 (17) ◽  
pp. 9792-9797
Author(s):  
Ming‐Qing Tian ◽  
Zhen‐Yao Shen ◽  
Xuefei Zhao ◽  
Patrick J. Walsh ◽  
Xu‐Hong Hu

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