## Abstract The hydroperoxy endoperoxide **3**, obtained by photooxygenation of isotetralin (= 1,4,5,8‐tetrahydronaphthalene; **1**), was reduced with thiourea, and the resulting intermediate **4** was converted, after acetylation with acetyl chloride, to the interesting, double‐chlorinated acetate
Regio- and Stereocontrolled Synthesis of (2R*,3R*,4R*)-3,4-Dichloro-1,2,3,4,5,8-hexahydronaphthalen-2-yl Acetate via Tandem SN2′ Reactions
✍ Scribed by Nurhan Horasan-Kishali; Ertan Sahin; Yunus Kara
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- German
- Weight
- 24 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0018-019X
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