Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine

Muhammad Sharif; Khurram Shoaib; Shahzad Ahmed; Jamshed Iqbal; Zharylkasyn A. Abilov; Anke Spannenberg; Peter Langer

doi:10.1016/j.tetlet.2016.05.041

Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine

Muhammad Sharif, Khurram Shoaib, Shahzad Ahmed, Jamshed Iqbal, Zharylkasyn A. Abilov, Anke Spannenberg, Peter Langer^*

^*Corresponding author for this work

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

10 Scopus citations

Abstract

3,5-Diaryl-2,4,6-trifluoropyridines and 5-aryl-3-chloro-2,4,6-trifluoropyridines were prepared through Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine with arylboronic acids in high yields.

Original language	English
Pages (from-to)	3060-3062
Number of pages	3
Journal	Tetrahedron Letters
Volume	57
Issue number	29
DOIs	https://doi.org/10.1016/j.tetlet.2016.05.041
State	Published - 2016
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2016

Keywords

Catalysis
Organofluorine compounds
Palladium
Pyridine
Suzuki–Miyaura reaction

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2016.05.041

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@article{9c91ffe59f654b7eab65e99cc9ab8e86,

title = "Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine",

abstract = "3,5-Diaryl-2,4,6-trifluoropyridines and 5-aryl-3-chloro-2,4,6-trifluoropyridines were prepared through Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine with arylboronic acids in high yields.",

keywords = "Catalysis, Organofluorine compounds, Palladium, Pyridine, Suzuki–Miyaura reaction",

author = "Muhammad Sharif and Khurram Shoaib and Shahzad Ahmed and Jamshed Iqbal and Abilov, \{Zharylkasyn A.\} and Anke Spannenberg and Peter Langer",

note = "Publisher Copyright: {\textcopyright} 2016",

year = "2016",

doi = "10.1016/j.tetlet.2016.05.041",

language = "English",

volume = "57",

pages = "3060--3062",

journal = "Tetrahedron Letters",

issn = "0040-4039",

number = "29",

}

TY - JOUR

T1 - Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine

AU - Sharif, Muhammad

AU - Shoaib, Khurram

AU - Ahmed, Shahzad

AU - Iqbal, Jamshed

AU - Abilov, Zharylkasyn A.

AU - Spannenberg, Anke

AU - Langer, Peter

PY - 2016

Y1 - 2016

N2 - 3,5-Diaryl-2,4,6-trifluoropyridines and 5-aryl-3-chloro-2,4,6-trifluoropyridines were prepared through Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine with arylboronic acids in high yields.

AB - 3,5-Diaryl-2,4,6-trifluoropyridines and 5-aryl-3-chloro-2,4,6-trifluoropyridines were prepared through Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine with arylboronic acids in high yields.

KW - Catalysis

KW - Organofluorine compounds

KW - Palladium

KW - Pyridine

KW - Suzuki–Miyaura reaction

UR - https://www.scopus.com/pages/publications/84975840784

U2 - 10.1016/j.tetlet.2016.05.041

DO - 10.1016/j.tetlet.2016.05.041

M3 - Article

AN - SCOPUS:84975840784

SN - 0040-4039

VL - 57

SP - 3060

EP - 3062

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 29

ER -

Suzuki–Miyaura reactions of 3,5-dichloro-2,4,6-trifluoropyridine

Abstract

Bibliographical note

Keywords

ASJC Scopus subject areas

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