Carbon–carbon bonding made easy

2005 ◽  
pp. 4759 ◽  
Author(s):  
Akira Suzuki
Keyword(s):  
Author(s):  
Wei Wang ◽  
Xinxin Li ◽  
Pan-Pan Zhou ◽  
Yao Wang
Keyword(s):  

2021 ◽  
Author(s):  
Wei Wang ◽  
Xinxin Li ◽  
Pan-Pan Zhou ◽  
Yao Wang
Keyword(s):  

1973 ◽  
Vol 248 (19) ◽  
pp. 6626-6629 ◽  
Author(s):  
Peter H. Haffner ◽  
Joseph E. Coleman

2018 ◽  
Vol 3 (35) ◽  
pp. 10032-10048
Author(s):  
Govindarajan Radha ◽  
Baskaran Vijaya Pandiyan ◽  
Palanisamy Deepa ◽  
Subbiah Govindarajan ◽  
Ponmalai Kolandaivel ◽  
...  

ChemPhysChem ◽  
2015 ◽  
Vol 16 (12) ◽  
pp. 2530-2533 ◽  
Author(s):  
Eduardo C. Escudero-Adán ◽  
Antonio Bauzá ◽  
Antonio Frontera ◽  
Pablo Ballester

Molecules ◽  
2019 ◽  
Vol 24 (18) ◽  
pp. 3370 ◽  
Author(s):  
Tiddo J. Mooibroek

A systematic evaluation of the CSD and the PDB in conjunction with DFT calculations reveal that non-covalent Carbon-bonding interactions with X–CH3 can be weakly directional in the solid state (P ≤ 1.5) when X = N or O. This is comparable to very weak CH hydrogen bonding interactions and is in line with the weak interaction energies calculated (≤ –1.5 kcal·mol−1) of typical charge neutral adducts such as [Me3N-CH3···OH2] (2a). The interaction energy is enhanced to ≤–5 kcal·mol−1 when X is more electron withdrawing such as in [O2N-CH3··O=Cdme] (20b) and to ≤18 kcal·mol−1 in cationic species like [Me3O+-CH3···OH2]+ (8a).


1991 ◽  
Vol 248 (1-2) ◽  
pp. 104-118 ◽  
Author(s):  
F.L. Hutson ◽  
D.E. Ramaker ◽  
B.E. Koel

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