Reactivity, selectivity and site activation are classical concepts in chemistry which are
amenable to quantitative representation, in terms of static global, local and non local density
response functions. The use of these electronic indexes describing chemical interconversion is
developed in thi...
Pérez, Patricia
,
Parra-Mouche, Julia
,
Contreras, Renato R.
,
[Quantitative representation of reactivity, selectivity and site activation concepts in organic chemistry]
,
Quantitative representation of reactivity, selectivity and site activation concepts in organic chemistry
The theoretical global and local electrophilicity patterns of substituted and chelated
4-oxo-4H-benzopyran-3-carbaldehydes (formylchromones) have been evaluated using the electrophilicity
index proposed by Parr et al [J. Am. Chem. Soc. 1999, 121, 1922]. The complexation of formylchromones
with al...
Araya Maturana, Ramiro
,
Heredia Moya, Jorge
,
Escobar, Carlos A.
,
Pérez, Patricia
,
[On the reduction of 4-oxo-4h-benzopyran-3-carbaldehydes : global and local electrophilicity patterns]
,
On the reduction of 4-oxo-4h-benzopyran-3-carbaldehydes : global and local electrophilicity patterns
Theoretical reactivity indices based on the conceptual Density Functional Theory (DFT) have become a powerful tool for the semiquantitative study of organic reactivity. A large number of reactivity indices have been proposed in the literature. Herein, global quantities like the electronic chemica...
Domingo, Luis R.
,
Ríos-Gutiérrez, Mar
,
Pérez, Patricia
,
[Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity]
,
Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity