Diversity-oriented synthesis of poly-substituted benzofuran derivatives bearing amino groups at 2- or 3-positions: Rh- or Ni-catalyzed cycloisomerization between ynamides and enol ethers

Amino-substituted benzofuran derivatives have attracted attention in recent years due to their remarkable biological activity.

Authors

Jun‐ya Hasegawa (ORCID: https://orcid.org/0000-0002-9700-3309)
Mitsuhiro Arisawa (ORCID: https://orcid.org/0000-0002-7937-670X)
Kazuhiro Uehara
Tomoyuki Tanaka (ORCID: https://orcid.org/0000-0002-9886-5947)
Makoto Sako (ORCID: https://orcid.org/0000-0002-4268-7002)
Hiromi Itakura
Kenichi Murai (ORCID: https://orcid.org/0000-0002-1689-6492)
Shohei Ohno (ORCID: https://orcid.org/0000-0002-2414-5066)
Ray Miyazaki (ORCID: https://orcid.org/0000-0001-7210-6646)
Jiawei Qiu

Institutions

Hokkaido University (JP)
The University of Osaka (JP)

Publication Details

Journal: Organic Chemistry Frontiers
Published: 2025-01-01
DOI: https://doi.org/10.1039/d5qo01123j
Citations: 1
Primary Topic: Catalytic Alkyne Reactions
Type: article
Field-Weighted Citation Impact: 0.94

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article

Diversity-oriented synthesis of poly-substituted benzofuran derivatives bearing amino groups at 2- or 3-positions: Rh- or Ni-catalyzed cycloisomerization between ynamides and enol ethers

Jun‐ya Hasegawa, Mitsuhiro Arisawa, Kazuhiro Uehara, Tomoyuki Tanaka et al.

Jan 1, 2025

1 citations

Organic Chemistry Frontiers

Catalytic Alkyne Reactions

0.94

article

Diversity-oriented synthesis of poly-substituted benzofuran derivatives bearing amino groups at 2- or 3-positions: Rh- or Ni-catalyzed cycloisomerization between ynamides and enol ethers

Jun‐ya Hasegawa, Mitsuhiro Arisawa, Kazuhiro Uehara, Tomoyuki Tanaka, Makoto Sako, Hiromi Itakura, Kenichi Murai, Shohei Ohno, Ray Miyazaki, Jiawei Qiu

January 1, 2025article en

1 citations

Abstract

Amino-substituted benzofuran derivatives have attracted attention in recent years due to their remarkable biological activity.

Organic Chemistry FrontiersVol. 12(22)

Hokkaido University (JP), The University of Osaka (JP)

Openalex Percentile: Top 21%

Catalytic Alkyne Reactions

0.94

DOI Source OpenAlex

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