Schleyer hyperconjugative aromaticity and Diels-Alder reactivity of 5-substituted cyclopentadienes.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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name

Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

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Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

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type

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label

Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

@en

Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

@nl

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Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

@en

Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

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P1476

Schleyer hyperconjugative arom ...... -substituted cyclopentadienes.

@en

P2093

Brian J Levandowski

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Lufeng Zou

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P2860

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Transition state distortion energies correlate with activation energies of 1,4-dihydrogenations and Diels-Alder cycloadditions of aromatic molecules.

Theoretical elucidation of the origins of substituent and strain effects on the rates of Diels-Alder reactions of 1,2,4,5-tetrazines.

Theory of 1,3-dipolar cycloadditions: distortion/interaction and frontier molecular orbital models.

Theoretical analysis of reactivity patterns in Diels-Alder reactions of cyclopentadiene, cyclohexadiene, and cycloheptadiene with symmetrical and unsymmetrical dienophiles.

The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other fun

P304

117-123

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scholarly article

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10.1002/JCC.24191

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P433

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P478

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Kendall Houk

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2015-10-07T00:00:00Z

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P5875

282659714

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26444427

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