Candida antarctica lipase B catalysed kinetic resolution of 1,2,3,4-tetrahydro-beta-carbolines Substrate specificity /
In the frame of substrate specificity, CAL-B-catalysed asymmetric N-alkoxycarbonylations of 1-substituted tetrahydro-beta-carbolines (Me, Et, Pr, iPr) have been studied. High enantioselectivities (>200) were observed, when alkoxycarbonylation of racemic compounds (+/-)-1,35,7 were performed in DI...
Elmentve itt :
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| Dokumentumtípus: | Cikk |
| Megjelent: |
2018
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| Sorozat: | TETRAHEDRON
74 No. 48 |
| doi: | 10.1016/j.tet.2018.10.034 |
| mtmt: | 30346733 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/14935 |
| Tartalmi kivonat: | In the frame of substrate specificity, CAL-B-catalysed asymmetric N-alkoxycarbonylations of 1-substituted tetrahydro-beta-carbolines (Me, Et, Pr, iPr) have been studied. High enantioselectivities (>200) were observed, when alkoxycarbonylation of racemic compounds (+/-)-1,35,7 were performed in DIPE in the presence of phenyl allyl carbonate and Et3N at 60 degrees C using ultrasound shaking method. The reaction time increased considerably with increasing substituent size on C1; however, the isopropyl-substituted compound proved to be too bulky for the optimum activity of CAL-B. The (R)-carbamate enantiomers were hydrolysed using Pd-2(dba)(3 center dot)CHCI3 and the enantiomers of the free amines were obtained with excellent ee (>99%). (C) 2018 Published by Elsevier Ltd. |
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| Terjedelem/Fizikai jellemzők: | 6873-6877 |
| ISSN: | 0040-4020 |