Suzuki-Miyaura coupling of benzylic carbonates with heteroarylboronic acids

Ryoichi Kuwano, Jung Yi Yu

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Cross-coupling of benzylic carbonates with heteroarylboronic acids successfully proceeded in the presence of the palladium catalyst that was generated in situ from [Pd(rf-C3Hs)CI]2 and a chelate bisphosphine DPPPent. Various heteroarylboronic acids were applicable to the catalytic cross-coupling, giving the desired benzylated heteroaromatics in high yields.

Original languageEnglish
Pages (from-to)233-237
Number of pages5
JournalHeterocycles
Volume74
Issue numberC
Publication statusPublished - Dec 31 2007

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Carbonates
Acids
Palladium
Catalysts
N-(3-N-(benzyloxycarbonyl)amino-1-carboxypropyl)leucyl-O-methyltyrosine N-methylamide

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Suzuki-Miyaura coupling of benzylic carbonates with heteroarylboronic acids. / Kuwano, Ryoichi; Yu, Jung Yi.

In: Heterocycles, Vol. 74, No. C, 31.12.2007, p. 233-237.

Research output: Contribution to journalArticle

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