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Solvolysis of derivatives of tricyclo (3.3.0.03,7) octan-2-ol

✍ Scribed by R.R. Sauers; B.R. Sickles


Publisher
Elsevier Science
Year
1970
Tongue
French
Weight
228 KB
Volume
11
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


A synthesis of tricyclo[3.3.0.03,7]Octan
✍ B.Richard Vogt; Stuart R. Suter; John R.E. Hoover πŸ“‚ Article πŸ“… 1968 πŸ› Elsevier Science 🌐 French βš– 220 KB

We wish to report the synthesis of tricyclo[3.3.0.03'7 ]octane (I) by a structurally unambiguous route and to describe the ring expansion of the derived carbinols II and III. Hydrocarbon I, for which we suggest the trivial name %isnoradamantane", may be regarded as a lower homolog of adamantane (IV)

The preparation and solvolysis of 2-chlo
✍ Peter K. Freeman; Robin B. Kinnel; Timothy D. Ziebarth πŸ“‚ Article πŸ“… 1970 πŸ› Elsevier Science 🌐 French βš– 221 KB

Our interest in the hydrocarbon tricyclo[3.3.0.0Jt7 Ioctane (l) has been stimulated by its bisnor relationship to adamantane (zero carbon bridges between C-l-C-5 and C-3-C-7 rather than one carbon bridges), its symmetry (Dad) and the fact that it contains the most twisted norbornane skeleton of reco

Simple Entry into Tricyclo[3.3.0.03,7]oc
✍ Hoffmann, H. Martin R. ;El-Khawaga, Ahmed M. ;Oehlerking, Hans-Heinrich πŸ“‚ Article πŸ“… 1991 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 115 KB
Die Cyclopropylcarbinyl-Cyclobutyl-Homoa
✍ Manfred Geisel; Cyril A. Grob; Werner Santi; Werner Tschudi πŸ“‚ Article πŸ“… 1973 πŸ› John Wiley and Sons 🌐 German βš– 737 KB

## 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