4.8 Article

Enantioselective Synthesis of 1-Aryl Benzo[5]helicenes Using BINOL-Derived Cationic Phosphonites as Ancillary Ligands

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 52, 页码 23527-23531

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202010021

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[5]helicenes; asymmetric catalysis; cationic phosphonites; gold catalysis; ligand design

资金

  1. Deutsche Forschungsgemeinschaft [Al 11348/4-3, INST 186/1237-1, INST 186/1298-1]

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The synthesis of unprecedented BINOL-derived cationic phosphonites is described. Through the use of these phosphanes as ancillary ligands in Au(I)catalysis, a highly regio- and enantioselective assembly of appropriately designed alkynes into 1-(aryl)benzo[5]carbohelicenes is achieved. The modular synthesis of these ligands and the enhanced reactivity that they impart to Au-I-centers after coordination have been found to be the key features that allow an optimization of the reaction conditions until the desired benzo[5]helicenes are obtained with high yield and enantioselectivity.

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