This title appears in the Scientific Report :
2001
Please use the identifier:
http://dx.doi.org/10.1039/b100341k in citations.
Please use the identifier: http://hdl.handle.net/2128/2437 in citations.
Please use the identifier: http://hdl.handle.net/2128/2833 in citations.
Enantioselective synthesis of hydroxy ketones through cleavage and formation of acyloin linkage : enzymatic kinetic resolution via C-C bond cleavage
Enantioselective synthesis of hydroxy ketones through cleavage and formation of acyloin linkage : enzymatic kinetic resolution via C-C bond cleavage
Both enantiomers of benzoins and (R)-2-hydroxy-1-phenylpropanone analogues were obtained in high yield on a preparative scale starting from aromatic aldehydes, rac-benzoins and aliphatic aldehydes via enzyme-catalysed C-C bond cleavage and C-C bond formation reactions.
Saved in:
Personal Name(s): | Demir, A. S. |
---|---|
Pohl, M. / Janzen, E. / Müller, M. | |
Contributing Institute: |
Biotechnologie 2; IBT-2 |
Published in: | Perkin transactions / 1 (2001) S. 633 - 635 |
Imprint: |
Cambridge [u.a.]
Royal Society of Chemistry
2001
|
Physical Description: |
633 - 635 |
DOI: |
10.1039/b100341k |
Document Type: |
Journal Article |
Research Program: |
Verfahrenstechnik zur mikrobiellen Gewinnung von Primärmetaboliten |
Series Title: |
Journal of the Chemical Society-Perkin Transactions 1
|
Subject (ZB): | |
Link: |
OpenAccess |
Publikationsportal JuSER |
Please use the identifier: http://hdl.handle.net/2128/2437 in citations.
Please use the identifier: http://hdl.handle.net/2128/2833 in citations.
Both enantiomers of benzoins and (R)-2-hydroxy-1-phenylpropanone analogues were obtained in high yield on a preparative scale starting from aromatic aldehydes, rac-benzoins and aliphatic aldehydes via enzyme-catalysed C-C bond cleavage and C-C bond formation reactions. |