## 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
Resolution of racemic 2,6,6-trimethyl-7-oxa-bicyclo[3.1.1]octan-2-ol and 1,6,6-trimethyl-7-oxa-bicyclo[3.1.1]octan-2-ol by microbial esterification
✍ Scribed by Mitsuo Miyazawa; Keisuke Tsuruno; Hiromu Kameoka
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 126 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
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✦ Synopsis
Resolution of racemic 2,6,
octan-2-ol and racemic 1,6,6-trimethyl-7-oxa-bicyclo[3.1,1 ]octan-2-ol via esterification with malonic acid by Glomerella cingulata, is described. Both of alcohols and malonic esters could be obtained in enantiomerically pure states. (~) 1997 Elsevier Science Ltd
📜 SIMILAR VOLUMES
## Abstract Preparation of the title compound (**4**) is described. An important transannular effect between the two unconjugated __s‐cis__‐butadiene chromophores is observed by comparison of the UV. spectra of the dimethylidene‐oxanorbornane **3** and the tetramethylidene‐oxanor‐bornane **4**.