Development of Pseudo-<i>C</i><sub>2</sub>-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp<sup>3</sup>)–H Functionalization Reactions under Rh(III) Catalysis
-
- Yoshimi Kato
- Faculty of Pharmaceutical Science, Hokkaido University, Sapporo 060-0812, Japan
-
- Luqing Lin
- Zhang Dayu School of Chemistry, Dalian University of Technology, Dalian 116024, Liaoning, China
-
- Masahiro Kojima
- Faculty of Pharmaceutical Science, Hokkaido University, Sapporo 060-0812, Japan
-
- Tatsuhiko Yoshino
- Faculty of Pharmaceutical Science, Hokkaido University, Sapporo 060-0812, Japan
-
- Shigeki Matsunaga
- Faculty of Pharmaceutical Science, Hokkaido University, Sapporo 060-0812, Japan
書誌事項
- 公開日
- 2021-03-22
- 資源種別
- journal article
- 権利情報
-
- https://doi.org/10.15223/policy-029
- https://doi.org/10.15223/policy-037
- https://doi.org/10.15223/policy-045
- DOI
-
- 10.1021/acscatal.1c00765
- 公開者
- American Chemical Society (ACS)
この論文をさがす
説明
Enantioselective C(sp3)–H functionalization reactions using high-valent group 9 metal catalysts with cyclopentadienyl ligands have been achieved by the introduction of appropriate chiral carboxylic...
収録刊行物
-
- ACS Catalysis
-
ACS Catalysis 11 (7), 4271-4277, 2021-03-22
American Chemical Society (ACS)
- Tweet
キーワード
- Enantioselective
- chiral carboxylic acids
- Chemical Sciences not elsewhere classified
- Immunology
- t Bu Rh III
- C 2
- substrate
- high-valent group 9 metal catalysts
- chiral carboxylic acid
- Biochemistry
- 333
- Environmental Sciences not elsewhere classified
- tunable chiral carboxylic acids
- Medicine
- Chiral Binaphthyl Monocarboxylic Acids
- Molecular Biology
- Biological Sciences not elsewhere classified
詳細情報 詳細情報について
-
- CRID
- 1360572092880416640
-
- ISSN
- 21555435
-
- 資料種別
- journal article
-
- データソース種別
-
- Crossref
- KAKEN
- OpenAIRE
