2010
DOI: 10.1016/j.tetasy.2010.04.025
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Chemoenzymatic method for the preparation of γ-amino alcohols from phenylfuran-based aldehydes; lipase-catalyzed kinetic resolution of β-hydroxy nitriles

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Cited by 8 publications
(2 citation statements)
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“…β ‐amino alcohols have been thoroughly studied, and synthetic approaches to access such molecules by chemical and biocatalytic ways are abundant . On the other hand, compounds containing γ‐amino alcohol are widely used for the treatment of psychiatric and metabolic disorders . γ ‐amino alcohols are also considered as efficient chelating agents applicable in asymmetric synthesis .…”
Section: Introductionmentioning
confidence: 99%
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“…β ‐amino alcohols have been thoroughly studied, and synthetic approaches to access such molecules by chemical and biocatalytic ways are abundant . On the other hand, compounds containing γ‐amino alcohol are widely used for the treatment of psychiatric and metabolic disorders . γ ‐amino alcohols are also considered as efficient chelating agents applicable in asymmetric synthesis .…”
Section: Introductionmentioning
confidence: 99%
“…[5] On the other hand, compounds containing g-amino alcohol are widely used for the treatment of psychiatric and metabolic disorders. [6] g-amino alcohols are also considered as efficient chelating agents applicable in asymmetric synthesis. [7] Despite the potential importance of g-amino alcohols, comparatively few methods for their preparations have been reported.…”
Section: Introductionmentioning
confidence: 99%