A direct entry to a semibullvalene structure by an abnormal diels-alder reaction. Mass spectrometry evidence of highly stable non-benzenoid aromatic cyclooctatetraene dications.-Reference-Cited by-同舟云学术

A direct entry to a semibullvalene structure by an abnormal diels-alder reaction. Mass spectrometry evidence of highly stable non-benzenoid aromatic cyclooctatetraene dications.

Published:1973-01 Issue:11 Volume:14 Page:821-824
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Serratosa F.,Solá P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. An approach to the synthesis of 1,2-dialkoxyacetylenes benzyne intermediates

2. Photo-oxidation of 1,2,3,4-tetrachloro-9,10-dihydro-9,10-dimethoxyetheno-anthracene

3. J. Font, A. Messeguer, F. Serratosa and L. Vilarrasa, International Symposium on Acetylenes, Allenes and Cumulenes, Nottingham, 5–8 July, 1971. Programme, p. 4;

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3. An approach to the synthesis of acetylene diethers via tetrachlorobenzyne. Methoxycarbynes versus dimethoxyacetylene;Tetrahedron;1975-01

4. ChemInform Abstract: EIN DIREKTER WEG ZU EINER SEMIBULLVALEN-STRUKTUR DURCH EINE ANOMALE DIELS-ALDER-RK., MASSENSPEKTROSKOPISCHE BEWEISE FUER SEHR STABILE, NICHT-BENZOIDE AROMATISCHE CYCLOOCTATETRAEN-DIKATIONEN;Chemischer Informationsdienst;1973-06-05

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