Enantioenriched Synthesis of C1-Symmetric BINOLs: Iron-Catalyzed Cross-Coupling of 2-Naphthols and Some Mechanistic Insight-Reference-Cited by-同舟云学术

Enantioenriched Synthesis of C1-Symmetric BINOLs: Iron-Catalyzed Cross-Coupling of 2-Naphthols and Some Mechanistic Insight

Published:2010-09-10 Issue:39 Volume:132 Page:13633-13635
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Egami Hiromichi¹,Matsumoto Kenji¹,Oguma Takuya¹,Kunisu Takashi¹,Katsuki Tsutomu¹

Affiliation:

1. Department of Chemistry, Faculty of Science, Graduate School, Kyushu University, and Institute for Advanced Study, Kyushu University, Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja105442m

Reference33 articles.

1. BINOL: A Versatile Chiral Reagent

2. Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon–carbon bond forming reactions

3. Chiral Phosphoric Acids: Powerful Organocatalysts for Asymmetric Addition Reactions to Imines

4. Stronger Brønsted Acids

5. Synthesis of enantiomerically pure binaphthyl derivatives. Mechanism of the enantioselective, oxidative coupling of naphthols and designing a catalytic cycle

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