(Q60323705)

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Quantitative characterization of the global electrophilicity pattern of some reagents involved in 1,3-dipolar cycloaddition reactions

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Quantitative characterization of the global electrophilicity pattern of some reagents involved in 1,3-dipolar cycloaddition reactions (English)

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Patricia Pérez

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Renato Contreras

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Renato Contreras

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4

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Luis R. Domingo

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Luis R. Domingo

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2

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author name string

M. José Aurell

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3

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publication date

April 2003

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published in

Tetrahedron

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volume

59

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issue

17

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page(s)

3117-3125

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cites work

Asymmetric 1,3-Dipolar Cycloaddition Reactions

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1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates

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7 January 2021

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Mechanism of 1,3-dipolar cycloadditions

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A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

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Orbital energy control of cycloaddition reactivity

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Stereoselective 1,3-dipolar cycloadditions of a chiral nitrone derived from erythrulose. An experimental and DFT theoretical study

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7 January 2021

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Electrophilicity Index

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Quantitative characterization of the global electrophilicity power of common diene/dienophile pairs in Diels–Alder reactions

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Density Functional Theory Study for the Cycloaddition of 1,3-Butadienes with Dimethyl Acetylenedicarboxylate. Polar Stepwise vs Concerted Mechanisms

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Density functional theory study of the cycloaddition reaction of furan derivatives with masked o-benzoquinones. Does the furan act as a dienophile in the cycloaddition reaction?

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Absolute hardness: companion parameter to absolute electronegativity

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10.1016/S0040-4020(03)00374-0

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(Q60323705)

Quantitative characterization of the global electrophilicity pattern of some reagents involved in 1,3-dipolar cycloaddition reactions

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