Sulfonamidoquinoline/palladium(II)-dimer complex as a catalyst precursor for palladium-catalyzed γ-Selective and stereospecific allyl-aryl coupling reaction between allylic acetates and arylboronic acids

Yusuke Makida; Hirohisa Ohmiya; Masaya Sawamura

doi:10.1002/asia.201000721

Sulfonamidoquinoline/palladium(II)-dimer complex as a catalyst precursor for palladium-catalyzed γ-Selective and stereospecific allyl-aryl coupling reaction between allylic acetates and arylboronic acids

Yusuke Makida, Hirohisa Ohmiya, Masaya Sawamura

Multidisciplinary chemistry

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

37 Citations (Scopus)

Abstract

On neutral territory: A neutral palladium(II)-dimer catalyst system incorporating anionic sulfonamidoquinoline ligands is effective for the γ-selective and stereospecific allyl-aryl coupling between acyclic (E)-allylic acetates and arylboronic acids.

Original language	English
Pages (from-to)	410-414
Number of pages	5
Journal	Chemistry - An Asian Journal
Volume	6
Issue number	2
DOIs	https://doi.org/10.1002/asia.201000721
Publication status	Published - Feb 1 2011

All Science Journal Classification (ASJC) codes

Biochemistry
Organic Chemistry

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Sulfonamidoquinoline/palladium(II)-dimer complex as a catalyst precursor for palladium-catalyzed γ-Selective and stereospecific allyl-aryl coupling reaction between allylic acetates and arylboronic acids. / Makida, Yusuke; Ohmiya, Hirohisa; Sawamura, Masaya.

In: Chemistry - An Asian Journal, Vol. 6, No. 2, 01.02.2011, p. 410-414.

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

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abstract = "On neutral territory: A neutral palladium(II)-dimer catalyst system incorporating anionic sulfonamidoquinoline ligands is effective for the γ-selective and stereospecific allyl-aryl coupling between acyclic (E)-allylic acetates and arylboronic acids.",

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Sulfonamidoquinoline/palladium(II)-dimer complex as a catalyst precursor for palladium-catalyzed γ-Selective and stereospecific allyl-aryl coupling reaction between allylic acetates and arylboronic acids

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