2011年11月4日
Synthesis of optically active N-aryl amino acid derivatives through the asymmetric petasis reaction catalyzed by a novel hydroxy-thiourea catalyst
Chemistry - An Asian Journal
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- ,
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- 巻
- 6
- 号
- 11
- 開始ページ
- 2902
- 終了ページ
- 2906
- 記述言語
- 英語
- 掲載種別
- 研究論文（学術雑誌）
- DOI
- 10.1002/asia.201100453
Thiourea makes peptides: Asymmetric Petasis reactions with vinylboronates and α-iminoamides are effectively catalyzed by the novel hydroxy-thiourea catalyst 1 (up to 86% yield, 93% ee
see scheme). This reaction can be applied not only to the synthesis of the unnatural amino acid monomers but also to peptide oligomers. © 2011 WILEY-VCH Verlag GmbH &
Co. KGaA, Weinheim.
see scheme). This reaction can be applied not only to the synthesis of the unnatural amino acid monomers but also to peptide oligomers. © 2011 WILEY-VCH Verlag GmbH &
Co. KGaA, Weinheim.
- ID情報
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- DOI : 10.1002/asia.201100453
- ISSN : 1861-4728
- ISSN : 1861-471X
- PubMed ID : 21815270
- SCOPUS ID : 80155150860