Item type |
学術雑誌論文 / Journal Article(1) |
公開日 |
2017-10-03 |
タイトル |
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タイトル |
Catalytic asymmetric dialkynylation reaction of α-dinitrone by utilizing tartaric acid ester as a chiral auxiliary |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
ID登録 |
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ID登録 |
10.24517/00010230 |
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ID登録タイプ |
JaLC |
著者 |
Serizawa, Masakazu
Fujinami, Shuhei
Ukaji, Yutaka
Inomata, Katsuhiko
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著者別表示 |
藤波, 修平
宇梶, 裕
猪股, 勝彦
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提供者所属 |
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内容記述タイプ |
Other |
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内容記述 |
金沢大学理工研究域物質化学系 |
書誌情報 |
Tetrahedron Asymmetry
巻 19,
号 8,
p. 921-931,
発行日 2008-05-01
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ISSN |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
0957-4166 |
NCID |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AA1074621X |
DOI |
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関連タイプ |
isIdenticalTo |
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識別子タイプ |
DOI |
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関連識別子 |
10.1016/j.tetasy.2008.03.033 |
出版者 |
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出版者 |
Elsevier |
抄録 |
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内容記述タイプ |
Abstract |
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内容記述 |
The asymmetric addition of alkynylzinc reagents, prepared in situ from dimethylzinc and 1-alkynes, to α-dinitrones derived from glyoxal and N-(4-isopropylbenzyl)hydroxylamine was investigated by utilizing dicyclohexyl (R,R)-tartrate as a chiral auxiliary. The addition reaction of methyl(2-phenylethynyl)zinc afforded the corresponding optically active C2-symmetric (R,R)-bis(hydroxylamine) derivative with enantioselectivities of 90% and 81% ee by utilizing a stoichiometric and catalytic amount of the tartrate, respectively. Furthermore, the catalytic addition reaction of several alkynylzinc reagents also furnished the corresponding bis(hydroxylamine) with moderate to good enantioselectivities. © 2008 Elsevier Ltd. All rights reserved. |
著者版フラグ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |