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 |
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container_title | Chemical communications (Cambridge, England) |
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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 |
format | Article |
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ispartof | Chemical communications (Cambridge, England), 2010-11, Vol.46 (42), p.8040-8042 |
issn | 1359-7345 1364-548X |
language | eng |
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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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