31032-94-7Relevant articles and documents
The Anion from 2,3-Dimethylnaphthalene/Tetramethylethylenediamine/n-Butyllithium: An Unusual Ambident Aromatic Nucleophile
Mitchell, Reginald H.,Dingle, Thomas W.,Williams, Richard Vaughan
, p. 903 - 905 (1983)
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Lewis acid catalyzed inverse electron-demand diels-alder reaction of 1,2-diazines
Kessler, Simon N.,Wegner, Hermann A.
supporting information; experimental part, p. 4062 - 4065 (2010/11/17)
A systematic approach toward Lewis acid catalyzed inverse electron-demand Diels-Alder (IEDDA) reactions of 1,2-diazines is described. The general concept is first investigated by DFT calculations, supported by spectroscopic data, and finally proven in the experiment.
Intramolecular Reaction Of Nitroxide Radicals With Biradical Intermediates Generated From Aromatic Enediynes
Grissom, Janet Wisniewski,Gunawardena, Gamini U.
, p. 4951 - 4954 (2007/10/02)
1,4-Dehydronaphthalene biradicals generated by thermolysis of aromatic enediynes can be trapped with the nitroxide radical TEMPO.The isolated products, however, are not the direct trapping products but 1,4-naphthoquinones resulting from the homolysis of N-O bonds of trapping products.