ChemInform Abstract: Palladium‐Catalyzed Diastereoselective Oxyarylation of 2‐Alkylindoles.

Vincenzo Ramella; Zhiheng He; Constantin G. Daniliuc; Armido Studer

doi:10.1002/chin.201525155

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ChemInform Abstract: Palladium‐Catalyzed Diastereoselective Oxyarylation of 2‐Alkylindoles.

Vincenzo Ramella Zhiheng He Constantin G. Daniliuc Armido Studer

Year: 2015 Journal: ChemInform Vol: 46 (25) Publisher: Wiley

DOI: 10.1002/chin.201525155

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Abstract

Abstract The title reaction uses commercially available boronic acids (II) as the aryl source and TEMPO as the oxidant and gives N‐protected (2‐chloroacetoxy)indolines in good yields with good to excellent diastereoselectivities.

Keywords:

Chemistry Aryl Palladium Catalysis Combinatorial chemistry Organic chemistry

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Catalytic C–H Functionalization Methods

Physical Sciences → Chemistry → Organic Chemistry

Oxidative Organic Chemistry Reactions

Physical Sciences → Chemistry → Organic Chemistry

Synthesis of Indole Derivatives

Physical Sciences → Chemistry → Organic Chemistry

ChemInform Abstract: Palladium‐Catalyzed Diastereoselective Oxyarylation of 2‐Alkylindoles.

Abstract

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