Unknown

Dataset Information

0

Au-Ag Bimetallic Catalysis: 3-Alkynyl Benzofurans from Phenols via Tandem C-H Alkynylation/Oxy-Alkynylation.


ABSTRACT: The development of new methodologies enabling a facile access to valuable heterocyclic frameworks still is an important subject of research. In this context, we describe a dual catalytic cycle merging C-H alkynylation of phenols and oxy-alkynylation of the newly introduced triple bond by using a unique redox property and the carbophilic π acidity of gold. Mechanistic studies support the participation of a bimetallic gold-silver species. The one-pot protocol offers a direct, simple, and regio-specific approach to 3-alkynyl benzofurans from readily available phenols. A broad range of substrates, including heterocycles, is transferred with excellent functional group tolerance. Thus, this methodology can be used for the late-stage incorporation of benzofurans.

SUBMITTER: Hu L 

PROVIDER: S-EPMC8252013 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Au-Ag Bimetallic Catalysis: 3-Alkynyl Benzofurans from Phenols via Tandem C-H Alkynylation/Oxy-Alkynylation.

Hu Long L   Dietl Martin C MC   Han Chunyu C   Rudolph Matthias M   Rominger Frank F   Hashmi A Stephen K ASK  

Angewandte Chemie (International ed. in English) 20210330 19


The development of new methodologies enabling a facile access to valuable heterocyclic frameworks still is an important subject of research. In this context, we describe a dual catalytic cycle merging C-H alkynylation of phenols and oxy-alkynylation of the newly introduced triple bond by using a unique redox property and the carbophilic π acidity of gold. Mechanistic studies support the participation of a bimetallic gold-silver species. The one-pot protocol offers a direct, simple, and regio-spe  ...[more]

Similar Datasets

| S-EPMC3778369 | biostudies-literature
| S-EPMC6414615 | biostudies-literature
| S-EPMC1762102 | biostudies-literature
| S-EPMC8503609 | biostudies-literature
| S-EPMC6843713 | biostudies-literature
| S-EPMC6731704 | biostudies-literature
| S-EPMC7559643 | biostudies-literature
| S-EPMC9642353 | biostudies-literature
| S-EPMC9078928 | biostudies-literature
| S-EPMC5562423 | biostudies-other