Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone

Shu Feng Zhao; Mei Xia Zhu; Kai Zhang; Huan Wang; Jia Xing Lu

doi:10.1016/j.tetlet.2011.03.076

Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone

Shu Feng Zhao
, Mei Xia Zhu
, Kai Zhang
, Huan Wang^*
, Jia Xing Lu

^*此作品的通讯作者

化学与分子工程学院

East China Normal University

科研成果: 期刊稿件 › 文章 › 同行评审

41 引用（Scopus）

摘要

The alkaloid-induced electrocarboxylation of 4-methylpropiophenone is examined in mild conditions. Comparative studies with several inductors indicate that the efficient enantiodiscrimination of the electrocarboxylation depends on the nucleophilic quinuclidine nitrogen atom and the OH group of the inductors.

源语言	英语
页（从-至）	2702-2705
页数	4
期刊	Tetrahedron Letters
卷	52
期	21
DOI	https://doi.org/10.1016/j.tetlet.2011.03.076
出版状态	已出版 - 25 5月 2011

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10.1016/j.tetlet.2011.03.076

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title = "Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone",

abstract = "The alkaloid-induced electrocarboxylation of 4-methylpropiophenone is examined in mild conditions. Comparative studies with several inductors indicate that the efficient enantiodiscrimination of the electrocarboxylation depends on the nucleophilic quinuclidine nitrogen atom and the OH group of the inductors.",

keywords = "Carbon dioxide, Cinchonine, Electrocarboxylation, Enantiomeric excess, Induction",

author = "Zhao, \{Shu Feng\} and Zhu, \{Mei Xia\} and Kai Zhang and Huan Wang and Lu, \{Jia Xing\}",

year = "2011",

month = may,

day = "25",

doi = "10.1016/j.tetlet.2011.03.076",

language = "英语",

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pages = "2702--2705",

journal = "Tetrahedron Letters",

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T1 - Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone

AU - Zhao, Shu Feng

AU - Zhu, Mei Xia

AU - Zhang, Kai

AU - Wang, Huan

AU - Lu, Jia Xing

PY - 2011/5/25

Y1 - 2011/5/25

N2 - The alkaloid-induced electrocarboxylation of 4-methylpropiophenone is examined in mild conditions. Comparative studies with several inductors indicate that the efficient enantiodiscrimination of the electrocarboxylation depends on the nucleophilic quinuclidine nitrogen atom and the OH group of the inductors.

AB - The alkaloid-induced electrocarboxylation of 4-methylpropiophenone is examined in mild conditions. Comparative studies with several inductors indicate that the efficient enantiodiscrimination of the electrocarboxylation depends on the nucleophilic quinuclidine nitrogen atom and the OH group of the inductors.

KW - Carbon dioxide

KW - Cinchonine

KW - Electrocarboxylation

KW - Enantiomeric excess

KW - Induction

UR - https://www.scopus.com/pages/publications/79955478769

U2 - 10.1016/j.tetlet.2011.03.076

DO - 10.1016/j.tetlet.2011.03.076

M3 - 文章

AN - SCOPUS:79955478769

SN - 0040-4039

VL - 52

SP - 2702

EP - 2705

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 21

ER -

Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone

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