抄録
The direct catalytic enantioselective α-aminooxylation of aldehydes has been developed using nitrosobenzene as the oxygen source and L-proline as catalyst, affording versatile α-aminooxylated aldehydes in high yield with excellent enantioselectivities.
| 元の言語 | English |
|---|---|
| ページ（範囲） | 8293-8296 |
| ページ数 | 4 |
| ジャーナル | Tetrahedron Letters |
| 巻 | 44 |
| 発行部数 | 45 |
| DOI | |
| 出版物ステータス | Published - 2003 11 3 |
| 外部発表 | Yes |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
これを引用
Direct proline catalyzed asymmetric α-aminooxylation of aldehydes. / Hayashi, Yujiro; Yamaguchi, Junichiro; Hibino, Kazuhiro; Shoji, Mitsuru.
：: Tetrahedron Letters, 巻 44, 番号 45, 03.11.2003, p. 8293-8296.研究成果: Article
}
TY - JOUR
T1 - Direct proline catalyzed asymmetric α-aminooxylation of aldehydes
AU - Hayashi, Yujiro
AU - Yamaguchi, Junichiro
AU - Hibino, Kazuhiro
AU - Shoji, Mitsuru
PY - 2003/11/3
Y1 - 2003/11/3
N2 - The direct catalytic enantioselective α-aminooxylation of aldehydes has been developed using nitrosobenzene as the oxygen source and L-proline as catalyst, affording versatile α-aminooxylated aldehydes in high yield with excellent enantioselectivities.
AB - The direct catalytic enantioselective α-aminooxylation of aldehydes has been developed using nitrosobenzene as the oxygen source and L-proline as catalyst, affording versatile α-aminooxylated aldehydes in high yield with excellent enantioselectivities.
KW - α-aminooxylation
KW - Asymmetric reaction
KW - Catalytic reaction
KW - Organocatalyst
KW - Proline
UR - http://www.scopus.com/inward/record.url?scp=0141957357&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0141957357&partnerID=8YFLogxK
U2 - 10.1016/j.tetlet.2003.09.057
DO - 10.1016/j.tetlet.2003.09.057
M3 - Article
AN - SCOPUS:0141957357
VL - 44
SP - 8293
EP - 8296
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 45
ER -