STRUCTURAL EVALUATION OF THE ENZYMATIC RESOLUTION OF TRICYCLO[5.2.1.02,6]DECENE-2-CARBOXYLATES USING PIG’S LIVER ESTERASE
Moderate to excellent entantio- and stereoselectivities (ee’s 54-100%) were observed in PLE catalyzed hydrolysis of (±)-ethyl 5-oxo-endo-tricyclo[5.2.1.02,6] deca-8-ene-2-carboxylate 5 and the structurally related open chain bicyclic structures (±)-ethyl 3-acetylbicyclo[2.2.1]hept-5-ene-2-carboxylat...
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| Format: | Article |
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| Language: | English |
| Published: |
University of Tehran
2000-09-01
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| Series: | Journal of Sciences, Islamic Republic of Iran |
| Online Access: | https://jsciences.ut.ac.ir/article_31839_1cc474b64bcd5ab8b4f82e98ca1565fe.pdf |
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| Summary: | Moderate to excellent entantio- and stereoselectivities (ee’s 54-100%) were observed in PLE catalyzed hydrolysis of (±)-ethyl 5-oxo-endo-tricyclo[5.2.1.02,6] deca-8-ene-2-carboxylate 5 and the structurally related open chain bicyclic structures (±)-ethyl 3-acetylbicyclo[2.2.1]hept-5-ene-2-carboxylates 7, 9 and (±)-ethyl 3-propanoylbicyclo[2.2.1]hept-5-ene-2-carboxylates 8, 10. A pronounced preference for hydrolysis of the exo- vs. the endo-ester function was observed. |
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| ISSN: | 1016-1104 2345-6914 |