Enantioselective catalytic borane reduction of prochiral ketones: Synthesis and application of new rigid β-amino alcohols with a cycloalkanol subunit

Article abstract of DOI:10.1080/00397919608003849

Enantiocontrolled reduction of prochiral ketones with borane in the presence of new enantiomerically pure bi- and tricyclic β-sec-amino alcohols 2-5 as stereodifferentiating catalysts afforded the optically active corresponding secondary alcohols in moder

Full text of DOI:10.1080/00397919608003849

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Enantioselective Catalytic
Borane Reduction of Prochiral
Ketones: Synthesis and
Application of New Rigid
β-Amino Alcohols with a
Cycloalkanol Subunit
Jörg Wilken a & Jürgen Martens a
a Fachbereich Chemie , Universität Oldenburg , P. O.
Box 2503, D-26111, Oldenburg, Federal Republic of
Germany E-mail:
Published online: 23 Aug 2006.
To cite this article: Jörg Wilken & Jürgen Martens (1996) Enantioselective Catalytic
Borane Reduction of Prochiral Ketones: Synthesis and Application of New Rigid
β-Amino Alcohols with a Cycloalkanol Subunit, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:23,
4477-4485, DOI: 10.1080/00397919608003849
To link to this article: http://dx.doi.org/10.1080/00397919608003849
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