Editorial [Hot Topic: Applications of Reactivity Indices based on Density Functional Theory to the Study of Organic Reactions. The Case of the Diels-Alder Reaction (Guest Editor: Luis R. Domingo)]

2011 ◽  
Vol 8 (2) ◽  
pp. 81-81 ◽  
Author(s):  
Luis R. Domingo
RSC Advances ◽  
2016 ◽  
Vol 6 (103) ◽  
pp. 101697-101706 ◽  
Author(s):  
Tuhin S. Khan ◽  
Shelaka Gupta ◽  
Md. Imteyaz Alam ◽  
M. Ali Haider

​The retro-Diels–Alder (rDA) reaction of partially saturated 2-pyrones were studied using density functional theory (DFT) calculations in polar and non-polar solvents, and fundamental descriptors were proposed to understand the electronic and solvent effect.


Synlett ◽  
2021 ◽  
Author(s):  
Takuya Kurahashi ◽  
Seijiro Matsubara ◽  
Rei Tomifuji ◽  
Shunpei Murano ◽  
Satoru Teranishi ◽  
...  

AbstractThe enantioselective oxa-Diels–Alder reaction of nonactivated substrates by utilizing FeCl3 and a 1,1′-bi-2-naphthol (BINOL) derived chiral phosphoric acid as a multiple activation catalyst is reported. Various oxygen-containing six-membered heterocycles were obtained in high yields and in an enantioselective manner. Density functional theory (DFT) calculations elucidate that both Lewis acidic and Brønsted acidic moieties in the catalyst system synergistically activate two lone pairs of an aldehyde to facilitate enantioselective addition reaction of dienes.


2020 ◽  
Vol 16 (4) ◽  
pp. 2172-2180
Author(s):  
Angela Acocella ◽  
Tainah D. Marforio ◽  
Matteo Calvaresi ◽  
Andrea Bottoni ◽  
Francesco Zerbetto

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