ListarArticles publicats (D-Q) por tema "Diels-Alder, Reacció de"

The reactivity of endohedral fullerenes: What can be learnt from computational studies?

Dispersion Corrections Essential for the Study of Chemical Reactivity in Fullerenes

The Exohedral Diels–Alder Reactivity of the Titanium Carbide Endohedral Metallofullerene Ti2C2@D3h-C78: Comparison with D3h-C78 and M3N@D3h-C78 (M=Sc and Y) Reactivity

Full Exploration of the Diels–Alder Cycloaddition on Metallofullerenes M3N@C80 (M=Sc, Lu, Gd): The D5h versus Ih Isomer and the Influence of the Metal Cluster

Electrochemical control of the regioselectivity in the exohedral functionalization of C60: The role of aromaticity

Why do cycloaddition reactions involving C60 prefer [6,6] over [5,6] bonds?

Diels-Alder and Retro-Diels-Alder cycloadditions of (1,2,3,4,5-pentamethyl)cyclopentadiene to La@C2v-C82: Regioselectivity and product stability

Corrigendum: Diels-Alder and Retro-Diels-Alder cycloadditions of (1,2,3,4,5-pentamethyl)cyclopentadiene to La@C2v-C82: Regioselectivity and product stability (Chemistry - A European Journal (2013) 19 DOI:10.1002/chem.201203517)

A complete guide on the influence of metal clusters in the diels-alder regioselectivity of Ih-C80 endohedral metallofullerenes

Origin of reactivity trends of noble gas endohedral fullerenes Ng2atC60(Ng = He to Xe)

Why bistetracenes are much less reactive than pentacenes in Diels-Alder reactions with fullerenes

Reactivity and selectivity of bowl-shaped polycyclic aromatic hydrocarbons: Relationship to C60

Understanding the Reactivity of Planar Polycyclic Aromatic Hydrocarbons: Towards the Graphene Limit

Predicting and Understanding the Reactivity of Aza[60]fullerenes

Is coronene better described by Clar's aromatic π-sextet model or by the AdNDP representation?

On the regioselectivity of the Diels–Alder cycloaddition to C60 in high spin states

Rationalizing the Regioselectivity of the Diels-Alder Bis-Cycloaddition of Fullerenes

Influence of the Charge on the Reactivity of Azafullerenes

Do Carbon Nano‐onions Behave as Nanoscopic Faraday Cages? A Comparison of the Reactivity of C60, C240, C60@C240, Li+@C60, Li+@C240, and Li+@C60@C240

Successive Diels–Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C60: A Computational Study

Regioselective access to orthogonal Diels-Alder C60 bis-adducts and tris-heteroadducts via supramolecular mask strategy