Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

Cedric W. Holzapfel; Catherine Dwyer

doi:10.3987/com-98-8197

Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

Cedric W. Holzapfel, Catherine Dwyer

Chemical Sciences

University of Johannesburg

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

19 Citations (Scopus)

Abstract

The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

Original language	English
Pages (from-to)	1513-1518
Number of pages	6
Journal	Heterocycles
Volume	48
Issue number	8
DOIs	https://doi.org/10.3987/com-98-8197
Publication status	Published - 1998

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles",

abstract = "The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.",

author = "Holzapfel, {Cedric W.} and Catherine Dwyer",

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AU - Holzapfel, Cedric W.

AU - Dwyer, Catherine

PY - 1998

Y1 - 1998

N2 - The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

AB - The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

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DO - 10.3987/com-98-8197

M3 - Article

AN - SCOPUS:0001661810

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JF - Heterocycles

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ER -

Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

Abstract

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