ChemInform Abstract: Oxidative Coupling of Aryl Boron Reagents with sp<sup>3</sup>‐Carbon Nucleophiles: The Enolate Chan—Evans—Lam Reaction.

Moon, Patrick J.; Halperin, Heather M.; Lundgren, Rylan J.

doi:10.1002/chin.201623060

ChemInform

2016

DOI: 10.1002/chin.201623060

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ChemInform Abstract: Oxidative Coupling of Aryl Boron Reagents with sp³‐Carbon Nucleophiles: The Enolate Chan—Evans—Lam Reaction.

Patrick J. Moon

Heather M. Halperin

Rylan J. Lundgren

Abstract: In this new oxidative method for the arylation of activated methylene species Cu(O‐Tf)2 mediates the selective coupling of functionalized aryl boron species with stabilized sp3‐nucleophiles.

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ChemInform Abstract: Oxidative Coupling of Aryl Boron Reagents with sp³‐Carbon Nucleophiles: The Enolate Chan—Evans—Lam Reaction.

Abstract: In this new oxidative method for the arylation of activated methylene species Cu(O‐Tf)2 mediates the selective coupling of functionalized aryl boron species with stabilized sp3‐nucleophiles.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Oxidative Coupling of Aryl Boron Reagents with sp3‐Carbon Nucleophiles: The Enolate Chan—Evans—Lam Reaction.

Abstract: In this new oxidative method for the arylation of activated methylene species Cu(O‐Tf)2 mediates the selective coupling of functionalized aryl boron species with stabilized sp3‐nucleophiles.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Oxidative Coupling of Aryl Boron Reagents with sp³‐Carbon Nucleophiles: The Enolate Chan—Evans—Lam Reaction.