Phosphinodifluoroalkylation of alkynes using P(O)H compounds and ethyl difluoroiodoacetate

Literature Information

Publication Date 2017-07-17
DOI 10.1039/C7QO00466D
Impact Factor 5.281
Authors

Pengbo Zhang, Jianxi Ying, Guo Tang


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Abstract

The first phosphinodifluoroalkylation of alkynes is achieved and the simultaneous addition of both difluoromethylene and phosphinoyl groups across the alkynes with high regio- and stereoselectivity is of great significance. By using palladium(II) chloride as a catalyst and Xantphos as a ligand, the reaction of P(O)H compounds, alkynes, and ethyl difluoroiodoacetate proceeds with moderate to high yields, and provides an attractive approach for the construction of (E)-γ,γ-difluoroalkenylphosphine oxides.

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Contents

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DOI: 10.1039/C0CP90048F

Back cover

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DOI: 10.1039/C0CP90005B

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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