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

^*Corresponding author for this work

Lamar University

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

5 Scopus citations

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.

Original language	English
Pages (from-to)	143-153
Number of pages	11
Journal	Journal of Fluorine Chemistry
Volume	53
Issue number	2
DOIs	https://doi.org/10.1016/S0022-1139(00)82336-2
State	Published - Jul 1991
Externally published	Yes

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10.1016/S0022-1139(00)82336-2

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@article{b4be9da7524e43999a1fa987a5d00edc,

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",

month = jul,

doi = "10.1016/S0022-1139(00)82336-2",

language = "英语",

volume = "53",

pages = "143--153",

journal = "Journal of Fluorine Chemistry",

issn = "0022-1139",

publisher = "Elsevier B.V.",

number = "2",

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TY - JOUR

T1 - A synthetic and MO-SCF study of the trifluoroethoxylation of trifluoromethylchloropyridine derivatives

AU - Xuhong, Qian

AU - Idoux, John P.

PY - 1991/7

Y1 - 1991/7

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

Abstract

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