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Aqueous chemoenzymatic one-pot enantioselective synthesis of tertiary α-aryl cycloketones via Pd-catalyzed C–C formation and enzymatic C=C asymmetric hydrogenation.
- Source :
- Green Chemistry; 3/7/2021, Vol. 23 Issue 5, p1960-1964, 5p
- Publication Year :
- 2021
-
Abstract
- An aqueous chemoenzymatic cascade reaction combining Pd-catalyzed C–C formation and enzymatic C=C asymmetric hydrogenation (AH) was developed for enantioselective synthesis of tertiary α-aryl cycloketones in good yields and excellent enantioselectivities. The stereopreference of the enzyme in AH of α-aryl cyclohexenones was studied. An enantiocomplementary enzyme was obtained by site-directed mutation. [ABSTRACT FROM AUTHOR]
- Subjects :
- HYDROGENATION
CYCLOHEXENONES
ENZYMES
Subjects
Details
- Language :
- English
- ISSN :
- 14639262
- Volume :
- 23
- Issue :
- 5
- Database :
- Complementary Index
- Journal :
- Green Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 149295369
- Full Text :
- https://doi.org/10.1039/d1gc00372k