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Enantioselective Ethylation of Various Aldehydes Catalyzed by Readily Accessible Chiral Diols.
- Source :
- Chirality; Aug2016, Vol. 28 Issue 8, p593-598, 6p
- Publication Year :
- 2016
-
Abstract
- Four chiral C<subscript>2</subscript>-symmetric diols were synthesized in a straightforward three-step reaction and demonstrated excellent and good overall yields. Their catalytic activities were examined via the addition of diethylzinc to various aldehydes. The of diethylzinc to 2-methoxybenzaldehyde gave the corresponding chiral secondary alcohol with high yields (up to 95%) and moderate to good enantiomeric excess (up to 88%). All synthesized ligands were evaluated in the addition of diethylzinc to various aldehydes in the presence of an additional metal such as Ti(IV) complexes. Chirality 28:593-598, 2016. © 2016 Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]
- Subjects :
- CHIRALITY
GLYCOLS
CATALYSIS
ENANTIOMERS
ALDEHYDES
Subjects
Details
- Language :
- English
- ISSN :
- 08990042
- Volume :
- 28
- Issue :
- 8
- Database :
- Complementary Index
- Journal :
- Chirality
- Publication Type :
- Academic Journal
- Accession number :
- 117023070
- Full Text :
- https://doi.org/10.1002/chir.22617