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

^*Corresponding author for this work

School of Chemistry and Molecular Engineering

East China Normal University

Research output: Contribution to journal › Article › peer-review

41 Scopus citations

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.

Original language	English
Pages (from-to)	2702-2705
Number of pages	4
Journal	Tetrahedron Letters
Volume	52
Issue number	21
DOIs	https://doi.org/10.1016/j.tetlet.2011.03.076
State	Published - 25 May 2011

Keywords

Carbon dioxide
Cinchonine
Electrocarboxylation
Enantiomeric excess
Induction

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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",

volume = "52",

pages = "2702--2705",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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TY - JOUR

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

Abstract

Keywords

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