Palladium-catalyzed bisolefination of C-C triple bonds: A facile method for the synthesis of naphthalene derivatives

Chao Feng; Teck Peng Loh

doi:10.1021/ja108998d

Palladium-catalyzed bisolefination of C-C triple bonds: A facile method for the synthesis of naphthalene derivatives

Chao Feng, Teck Peng Loh^*

^*Corresponding author for this work

Nanyang Technological University

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

88 Citations (Scopus)

Abstract

A highly efficient and mild palladium-mediated bisolefination of C-C triple bonds is described for the first time. With different types of olefin employed, this reaction terminates in diverse fashions. In addition to the merit of using oxygen as the sole oxidant, this reaction exhibits high reactivities and functionality tolerance simultaneously, thus providing a promising method for the synthesis of naphthalene derivatives.

Original language	English
Pages (from-to)	17710-17712
Number of pages	3
Journal	Journal of the American Chemical Society
Volume	132
Issue number	50
DOIs	https://doi.org/10.1021/ja108998d
Publication status	Published - Dec 22 2010
Externally published	Yes

ASJC Scopus Subject Areas

Catalysis
General Chemistry
Biochemistry
Colloid and Surface Chemistry

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10.1021/ja108998d

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abstract = "A highly efficient and mild palladium-mediated bisolefination of C-C triple bonds is described for the first time. With different types of olefin employed, this reaction terminates in diverse fashions. In addition to the merit of using oxygen as the sole oxidant, this reaction exhibits high reactivities and functionality tolerance simultaneously, thus providing a promising method for the synthesis of naphthalene derivatives.",

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Palladium-catalyzed bisolefination of C-C triple bonds: A facile method for the synthesis of naphthalene derivatives

Abstract

ASJC Scopus Subject Areas

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