Catalytic enantioselective reactions. Part 7. Synthesis of new β-aminoalcohols derived from α-D-glucose as chiral catalysts for the catalytic enantioselective addition of diethylzinc to aldehydes

Article abstract of DOI:10.1080/00397919608003689

A series of new 1,2-O-isopropylidene-3-O-methyl-6-deoxy-6-N,N-dialkylamino-α-D-glucof uranoses 1 and 1,2-O-isopropylidene-3,6-dideoxy-6-N,N-dialkylamino-α-D-glucofuranose s 1' were prepared from α-D-glucose and their enantioselectivities compared as chiral catalysts for the ethylation of benzaldehyde and heptanal with diethylzinc.

Full text of DOI:10.1080/00397919608003689

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Synthetic Communications:
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Catalytic Enantioselective
Reactions Part 7. Synthesis
of New β-Aminoalcohols
Derived from α-D-Glucose
as Chiral Catalysts for the
Catalytic Enantioselective
Addition of Diethylzinc to
Aldehydes
Byung Tae Cho a & Namdu Kim a
a Department of Chemistry , Hallym University ,
Chunchon, 200–702, Republic of Korea
Published online: 21 Aug 2006.
To cite this article: Byung Tae Cho & Namdu Kim (1996) Catalytic
Enantioselective Reactions Part 7. Synthesis of New β-Aminoalcohols Derived
from α-D-Glucose as Chiral Catalysts for the Catalytic Enantioselective Addition
of Diethylzinc to Aldehydes, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 26:5, 855-865, DOI:
10.1080/00397919608003689
To link to this article: http://dx.doi.org/10.1080/00397919608003689
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