Journal article
Electrophilic substitution with allylic rearrangement (SE′). Syn-stereospecificity accompanying sulfur dioxide insertion into 4- and 6-alkylcyclohex-2-enyltrimethylstannanes
Tetrahedron Letters, Vol.24(51), pp.5793-5796
1983
Abstract
Sulfur dioxide insertion (chloroform solvent) into cis and trans-4 and -6-methyl- and 4-t-butylcyclohex-2-enyltrimethylstannanes is γ-regio and syn-stereospecific and hence less sensitive to steric effects by δ-substituents than trifluoroacetolysis (CF3COOD in CHCl3). © 1983.
Details
- Title
- Electrophilic substitution with allylic rearrangement (SE′). Syn-stereospecificity accompanying sulfur dioxide insertion into 4- and 6-alkylcyclohex-2-enyltrimethylstannanes
- Authors
- David James Young (Author) - University of QueenslandW Kitching (Author) - University of Queensland
- Publication details
- Tetrahedron Letters, Vol.24(51), pp.5793-5796
- Publisher
- Pergamon
- Date published
- 1983
- DOI
- 10.1016/S0040-4039(00)94203-5
- ISSN
- 0040-4039
- Organisation Unit
- University of the Sunshine Coast, Queensland
- Language
- English
- Record Identifier
- 99449284702621
- Output Type
- Journal article
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