Abstract
Bis-sulphonium salts of naphthalene derivatives have been synthesized in good yields via the reaction of dimethyl sulphide with primary naphthyl halides under mild conditions.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
4 articles.
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1. Unique behavior of 2,6-bis(bromomethyl)naphthalene as a highly active organic DNA crosslinking molecule;Bioorganic & Medicinal Chemistry;2009-05
2. Scope and Limitations of a New Highly Selective Synthesis of Unsymmetrical Monomers for the Synthesis of Precursors toward Poly(arylenevinylene)s;The Journal of Organic Chemistry;1999-12-29
3. Photoisomerization of tetraethyl 6,8,15,17-tetrahydro-7H,16H-5,18[1',2']-benzeno-9,14-ethenodibenzo[a,h]cyclotetradecene-7,7,16,16-tetracarboxylate. Structure of tetraethyl 2,3,3a,7b,9,10,10a,14b-hexahydro-1H,8H-3a,7b[1',2']-benzeno-10a,14b-ethenodibenzo[a,e]dicyclopenta[c,g]cyclooctene-2,2,9,9-tetracarboxylate as its methylene chloride solvate;Acta Crystallographica Section C Crystal Structure Communications;1994-07-15
4. An exceptionally simple method of preparation of biradicals. 2. Low-temperature fluorescence spectra and ambient temperature laser-induced fluorescence spectra of 1,3-, 1,6-, 2,6-, and 2,7-naphthoquinodimethane;Journal of the American Chemical Society;1991-01