Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5277674 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Thioketene S,S-dioxides 2 were successfully generated through [3,3] sigmatropic rearrangement of alkynyl propargyl sulfones 1 and the formation of 2 was confirmed by trapping experiment using cyclohexene or allyltrimethylsilane affording a [2+2] cycloadduct 5. In situ generated thioketene S,S-dioxides 2 underwent facile conversion into allenynes 3 in moderate yields, via formation and subsequent [1,2] shift of vinylidene carbenes.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shigenobu Aoyagi, Makoto Koyanagi, Megumi Takahashi, Kazuaki Shimada, Yuji Takikawa,