(Q46941945)

26 December 2017

title

Cu-catalyzed Goldberg and Ullmann reactions of aryl halides using chelating N- and O-based ligands (English)

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26 December 2017

author

Ryan A. Altman

series ordinal

1

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26 December 2017

Stephen L. Buchwald

series ordinal

2

object named as

Stephen L Buchwald

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26 December 2017

publication date

1 January 2007

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26 December 2017

published in

Nature Protocols

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26 December 2017

volume

2

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26 December 2017

issue

10

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26 December 2017

page(s)

2474-2479

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Total synthesis of reblastatin

cites work

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Modern Synthetic Methods for Copper-Mediated C(aryl)–O, C(aryl)–N, and C(aryl)–S Bond Formation

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A general and efficient copper catalyst for the amidation of aryl halides

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A General and Efficient Copper Catalyst for the Amidation of Aryl Halides and theN-Arylation of Nitrogen Heterocycles

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Mild and efficient copper-catalyzed amination of aryl bromides with primary alkylamines.

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Highly selective room-temperature copper-catalyzed C-N coupling reactions

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The copper-catalyzed N-arylation of indoles

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Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles

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4,7-Dimethoxy-1,10-phenanthroline: an excellent ligand for the Cu-catalyzed N-arylation of imidazoles

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Copper-Catalyzed Coupling of Amides and Carbamates with Vinyl Halides

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A Domino Copper-Catalyzed C−O Coupling−Claisen Rearrangement Process

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A general, efficient, and inexpensive catalyst system for the coupling of aryl iodides and thiols

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Copper-catalyzed C-P bond construction via direct coupling of secondary phosphines and phosphites with aryl and vinyl halides.

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Copper-catalyzed domino halide exchange-cyanation of aryl bromides

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A general and mild copper-catalyzed arylation of diethyl malonate

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Copper-catalyzed halogen exchange in aryl halides: an aromatic Finkelstein reaction

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Cu-catalyzed N-arylation of oxazolidinones: an efficient synthesis of the kappa-opioid receptor Agonist CJ-15161.

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Rapid chromatographic technique for preparative separations with moderate resolution

31 March 2020

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https://api.crossref.org/works/10.1038%2FNPROT.2007.364

31 March 2020

Identifiers

DOI

10.1038/NPROT.2007.364

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26 December 2017

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26 December 2017