## Abstract Tricyclo[3.2.1.0^2,7^]octan‐3‐ol (**1**) and its 4‐isomer **7** were obtained by hydroboration of tricyclo[3.2.1.0^2,7^]oct‐3‐ene (**5**). The former alcohol **1** is quantitatively converted to the isomeric alcohol __exo__‐bicyclo[3.2.1]oct‐2‐en‐7‐ol (**3**) by treatment with aqueous a
2-Methyltricyclo[3.2.1.02,7]octan-6-ol, ein Modell für die Fragmentierung von Helifulvanolsäure
✍ Scribed by Bohlmann, Ferdinand ;Rotard, Wolfgang
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 174 KB
- Volume
- 1982
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
2‐Methyltricyclo[3.2.1.0^2,7^]octan‐6‐ol, a Model for the Fragmentation of Helifulvanolic Acid
The epimeric 2‐methyltricyclo[3.2.1.0^2,7^]octan‐6‐ols 7 and 8, models for the fragmentation of helifulvanolic acid, have been synthesized starting from 4‐methyl‐3‐cyclohexenecarboxylic acid. While an oxidative fragmentation of 7 and 8 could not be observed, a very similar fragmentation of both tosylates 9 and 10 occurred.
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