Transition-metal-mediated thiosulfinate ester synthesis
Unlike sulfur dioxide (SO{sub 2}), the coordination and organic reaction chemistry of disulfur monoxide (S{sub 2}O) has received little attention. A few Diels-Alder reactions of simple dienes with S{sub 2}O have been reported. However, there were no reports of direct S{sub 2}O complex synthesis prio...
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Veröffentlicht in: | Journal of the American Chemical Society 1989-10, Vol.111 (21), p.8268-8270 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Unlike sulfur dioxide (SO{sub 2}), the coordination and organic reaction chemistry of disulfur monoxide (S{sub 2}O) has received little attention. A few Diels-Alder reactions of simple dienes with S{sub 2}O have been reported. However, there were no reports of direct S{sub 2}O complex synthesis prior to our initial work. The authors recently published a synthesis of 4,5-diphenyl-3,6-dihydro-1,2-dithiin 1-oxide (2) which liberates S{sub 2}O via a transition-metal-assisted retro-Diels-Alder reaction. Here we report further on the unusual reactivity of 2 and its utilization in the synthesis of cyclic thiosulfinate esters. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja00203a033 |