One-pot sequential alcohol oxidation and asymmetric α-oxyamination in aqueous media using recyclable resin-supported peptide catalyst

An efficient tandem reaction system was developed, in which primary alcohols were used for the oxidation to the corresponding aldehydes followed by an asymmetric α-oxyamination with a resin-supported peptide catalyst.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2010-11, Vol.46 (42), p.8040-8042
Hauptverfasser: Akagawa, Kengo, Fujiwara, Takuma, Sakamoto, Seiji, Kudo, Kazuaki
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container_end_page 8042
container_issue 42
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container_title Chemical communications (Cambridge, England)
container_volume 46
creator Akagawa, Kengo
Fujiwara, Takuma
Sakamoto, Seiji
Kudo, Kazuaki
description An efficient tandem reaction system was developed, in which primary alcohols were used for the oxidation to the corresponding aldehydes followed by an asymmetric α-oxyamination with a resin-supported peptide catalyst.
doi_str_mv 10.1039/c0cc02301a
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source MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Alcohols - chemistry
Amines - chemistry
Catalysis
Oxidation-Reduction
Peptides - chemistry
Water
title One-pot sequential alcohol oxidation and asymmetric α-oxyamination in aqueous media using recyclable resin-supported peptide catalyst
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