Synthesis, Structure, and Thermolysis of Tris(dimethylphenylsilyl)methyl Sulfenyl Chloride
Sulfenyl chlorides, i.e., di-coordinated sulfur(II) chlorides are useful precursors for a variety of organic sulfur compounds. Herein, the synthesis, structure, and reactivity of a sulfenyl chloride that bears a bulky tris(dimethylphenylsilyl)methyl group on the sulfur atom are reported. The thermol...
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Published in: | Chemistry letters Vol. 46; no. 6; pp. 837 - 839 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English Japanese |
Published: |
Tokyo
The Chemical Society of Japan
05-06-2017
Chemical Society of Japan |
Subjects: | |
Online Access: | Get full text |
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Summary: | Sulfenyl chlorides, i.e., di-coordinated sulfur(II) chlorides are useful precursors for a variety of organic sulfur compounds. Herein, the synthesis, structure, and reactivity of a sulfenyl chloride that bears a bulky tris(dimethylphenylsilyl)methyl group on the sulfur atom are reported. The thermolysis of this sulfenyl chloride resulted in the generation of the corresponding bissilylthioketone via the 1,2-elimination of chlorodimethylphenylsilane. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.170188 |