## 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
✦ LIBER ✦
Endo- und exo- 6.7-benzo-8-oxa-1.5-diphenyl-tricyclo[3.2.1.02.4]octen und ihr verhalten bei säurebehandlung.
✍ Scribed by Kurt Geibel; Josef Heindl
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 182 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Die Cyclopropylcarbinyl-Cyclobutyl-Homoa
✍
Manfred Geisel; Cyril A. Grob; Werner Santi; Werner Tschudi
📂
Article
📅
1973
🏛
John Wiley and Sons
🌐
German
⚖ 737 KB
Die Cyclopropylcarbinyl-Cyclobutyl-Homoa
✍
Manfred Geisel; Cyril A. Grob; Werner Santi; Werner Tschudi
📂
Article
📅
1973
🏛
John Wiley and Sons
🌐
German
⚖ 524 KB
## Abstract Solvolyses of the 2,4‐dinitrobenzoates of the cyclopropylcarbinol **1a**, the cyclo‐butanol **2a** and the homoallylic alcohol **3a** in buffered 70% aqueous dioxane lead to the same product mixture consisting of 78% cyclopropylcarbinol **1a** and 22% homoallylic alcohol **3a**. Approxi
In vivo- und in vitro-Untersuchung von s
✍
R. Neidlein; H.-P. Deigner; W. Kramer
📂
Article
📅
1988
🏛
John Wiley and Sons
🌐
English
⚖ 473 KB
👁 2 views
The photolysis of exo-1,6-dimethyl-7,8-d
✍
I.W. McCay; R.N. Warrener
📂
Article
📅
1970
🏛
Elsevier Science
🌐
French
⚖ 201 KB