Reactions of Cage Substrates with Sulfur Nucleophiles
Reactions of alcohols of the adamantane series and adamantan-1-yl nitrates with sulfur nucleophiles in 94% sulfuric acid afforded a number of new sulfur-containing adamantane derivatives such as carbamothioates, isothiocyanates, and carbamodithioates. Di(adamantan-1-yl) disulfide was synthesized by...
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Veröffentlicht in: | Russian journal of organic chemistry 2021-03, Vol.57 (3), p.355-363 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Reactions of alcohols of the adamantane series and adamantan-1-yl nitrates with sulfur nucleophiles in 94% sulfuric acid afforded a number of new sulfur-containing adamantane derivatives such as carbamothioates, isothiocyanates, and carbamodithioates. Di(adamantan-1-yl) disulfide was synthesized by reaction of admantan-1-yl nitrate with sodium sulfide nonahydrate in 94% sulfuric acid. |
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ISSN: | 1070-4280 1608-3393 |
DOI: | 10.1134/S1070428021030052 |