Issue 1, 2018

Rh(iii)-Catalyzed ortho-C–H alkynylation of N-phenoxyacetamides with hypervalent iodine-alkyne reagents at room temperature

Abstract

A Rh(III)-catalyzed C–H alkynylation of substituted N-phenoxyacetamides has been developed with the aid of hypervalent iodine-alkyne reagents. Complementary to the Sonogashira coupling reaction, this protocol provides an efficient and straightforward method to access aryl alkynes at room temperature. The multifunctional directing group is preserved which can be further employed for ortho-directed functionalizations to obtain additional new complex products.

Graphical abstract: Rh(iii)-Catalyzed ortho-C–H alkynylation of N-phenoxyacetamides with hypervalent iodine-alkyne reagents at room temperature

Supplementary files

Article information

Article type
Communication
Submitted
29 Sep 2017
Accepted
28 Nov 2017
First published
28 Nov 2017

Org. Biomol. Chem., 2018,16, 43-47

Rh(III)-Catalyzed ortho-C–H alkynylation of N-phenoxyacetamides with hypervalent iodine-alkyne reagents at room temperature

S. Hu, L. Lu, T. Zhu, Q. Wu, Y. Chen, J. J. Li and J. Zhao, Org. Biomol. Chem., 2018, 16, 43 DOI: 10.1039/C7OB02438J

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