A synthetic and MO-SCF study of the trifluoroethoxylation of trifluoromethylchloropyridine derivatives

Qian Xuhong; John P. Idoux

doi:10.1016/S0022-1139(00)82336-2

A synthetic and MO-SCF study of the trifluoroethoxylation of trifluoromethylchloropyridine derivatives

Qian Xuhong^*
, John P. Idoux

^*此作品的通讯作者

Lamar University

科研成果: 期刊稿件 › 文章 › 同行评审

5 引用（Scopus）

摘要

The trifluoroethoxylation of a series of trifluoromethylchloropyridines was studied. The reactivity, selectivity and leaving ability of the chloro- and trifluoromethyl- group were discussed. The influence of different substituents on the reactivity of the pyridine ring was also studied using the molecular orbital method.

源语言	英语
页（从-至）	143-153
页数	11
期刊	Journal of Fluorine Chemistry
卷	53
期	2
DOI	https://doi.org/10.1016/S0022-1139(00)82336-2
出版状态	已出版 - 7月 1991
已对外发布	是

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title = "A synthetic and MO-SCF study of the trifluoroethoxylation of trifluoromethylchloropyridine derivatives",

abstract = "The trifluoroethoxylation of a series of trifluoromethylchloropyridines was studied. The reactivity, selectivity and leaving ability of the chloro- and trifluoromethyl- group were discussed. The influence of different substituents on the reactivity of the pyridine ring was also studied using the molecular orbital method.",

author = "Qian Xuhong and Idoux, \{John P.\}",

year = "1991",

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AU - Idoux, John P.

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N2 - The trifluoroethoxylation of a series of trifluoromethylchloropyridines was studied. The reactivity, selectivity and leaving ability of the chloro- and trifluoromethyl- group were discussed. The influence of different substituents on the reactivity of the pyridine ring was also studied using the molecular orbital method.

AB - The trifluoroethoxylation of a series of trifluoromethylchloropyridines was studied. The reactivity, selectivity and leaving ability of the chloro- and trifluoromethyl- group were discussed. The influence of different substituents on the reactivity of the pyridine ring was also studied using the molecular orbital method.

UR - https://www.scopus.com/pages/publications/44949270329

U2 - 10.1016/S0022-1139(00)82336-2

DO - 10.1016/S0022-1139(00)82336-2

M3 - 文章

AN - SCOPUS:44949270329

SN - 0022-1139

VL - 53

SP - 143

EP - 153

JO - Journal of Fluorine Chemistry

JF - Journal of Fluorine Chemistry

IS - 2

ER -

A synthetic and MO-SCF study of the trifluoroethoxylation of trifluoromethylchloropyridine derivatives

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