(Q44963998)

English

Carbocationic rearrangement of pivaloyl cation and protonated pivalaldehyde in superacid medium: a novel solution equivalent of the McLafferty rearrangement

scientific article published in July 2004

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 December 2017

Carbocationic rearrangement of pivaloyl cation and protonated pivalaldehyde in superacid medium: a novel solution equivalent of the McLafferty rearrangement (English)

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Europe PubMed Central

PubMed publication ID

7 December 2017

author name string

George A Olah

1

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7 December 2017

Thomas Mathew

2

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7 December 2017

Alain Goeppert

3

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Europe PubMed Central

PubMed publication ID

7 December 2017

Golam Rasul

4

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7 December 2017

G K Surya Prakash

5

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7 December 2017

Pierre Mothé Esteves

6

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7 December 2017

publication date

1 July 2004

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7 December 2017

Journal of the American Society for Mass Spectrometry

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7 December 2017

15

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7 December 2017

7

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7 December 2017

959-965

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Europe PubMed Central

PubMed publication ID

7 December 2017

https://scigraph.springernature.com/pub.10.1016/j.jasms.2004.05.002

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Acid-catalyzed isomerization of pivalaldehyde to methyl isopropyl ketone via a reactive protosolvated carboxonium ion intermediate

1 reference

https://api.crossref.org/works/10.1016%2FJ.JASMS.2004.05.002

21 January 2018

Transition structures for hydrogen atom transfers to oxygen. Comparisons of intermolecular and intramolecular processes, and open- and closed-shell systems

1 reference

https://api.crossref.org/works/10.1016%2FJ.JASMS.2004.05.002

21 January 2018

Electrophilic reactions at single bonds. XVIII. Indication of protosolvated de facto substituting agents in the reactions of alkanes with acetylium and nitronium ions in superacidic media

1 reference

https://api.crossref.org/works/10.1016%2FJ.JASMS.2004.05.002

21 January 2018

Superelectrophiles

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https://api.crossref.org/works/10.1016%2FJ.JASMS.2004.05.002

21 January 2018

Synthetic methods and reactions. 63. Pyridinium poly(hydrogen fluoride) (30% pyridine-70% hydrogen fluoride): a convenient reagent for organic fluorination reactions

1 reference

https://api.crossref.org/works/10.1016%2FJ.JASMS.2004.05.002

21 January 2018

Identifiers

10.1016/J.JASMS.2004.05.002

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

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