Journal article
Electrophilic substitution with allylic rearrangement (SE′). Syn stereoselectivity in sulfur dioxide insertion into some cyclohex-2-enylstannanes
Journal of Organic Chemistry, Vol.48(4), pp.614-615
1983
Abstract
Sulfur dioxide insertion into cis- and trans-(5-alkylcyclohex-2-enyl)trimethylstannanes is demonstrated to be γ regio- and syn stereospecific, in contrast to the γ regiospecific but anti stereoselective trifluoro-acetolyses of these stannanes. © 1983 American Chemical Society.
Details
- Title
- Electrophilic substitution with allylic rearrangement (SE′). Syn stereoselectivity in sulfur dioxide insertion into some cyclohex-2-enylstannanes
- Authors
- David James Young (Author) - University of QueenslandW Kitching (Author) - University of Queensland
- Publication details
- Journal of Organic Chemistry, Vol.48(4), pp.614-615
- Publisher
- American Chemical Society
- Date published
- 1983
- DOI
- 10.1021/jo00152a045
- ISSN
- 0022-3263
- Organisation Unit
- University of the Sunshine Coast, Queensland
- Language
- English
- Record Identifier
- 99450083402621
- Output Type
- Journal article
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- Chemistry, Organic
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