Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1.

Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Research Abstract Details 

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Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Abstract Text:

Anthony J Fletcher,Matthew N Bax,Michael C Willis,Anthony J Fletcher,Matthew N Bax,Michael C Willis,

Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of indoles bearing sterically demanding N-substituents, including the natural product demethylasterriquinone A1.

Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Publishing Authors By Initials

AJ Fletcher,MN Bax,MC Willis,AJ Fletcher,MN Bax,MC Willis,

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Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Chemical communications (Cambridge, England)

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Page Numbers: 4764-6

Journal Abbreviation: Chem. Commun. (Camb.)

ISSN: 1359-7345

DAY: 3

MONTH: 09

YEAR: 2007

Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1. Information

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LANGUAGE: eng

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Grant and Affiliation Information for Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1.

AFFILIATION: Department of Chemistry, University of Oxford, Chemical Research Laboratory, Mansfield Road, Oxford, UKOX1 3TA. michael.willis@chem.ox.ac.uk.

Country: England

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MEDLINETA: Chem Commun (Camb)

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