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Catalytic Asymmetric Substitution Reaction of 3-Substituted 2-Indolylmethanols with 2-Naphthols

Feng Gao, Yu‐Chen Zhang, Feng Shi, Jin-Ping Lan, Yi‐Nan Lu, Ke-Wei Chen, Fei Jiang

2020Synthesis30 citationsDOI

Abstract

A catalytic asymmetric substitution of 3-substituted 2-indolylmethanols with 2-naphthols has been established under the catalysis of chiral phosphoric acid. By this approach, a series of structurally diversified triarylmethane derivatives were obtained in moderate to high yields with good enantioselectivities (up to 97% yield, 95:5 er). This approach not only enriches the chemistry of 2-indolylmethanol-inolved catalytic asymmetric substitutions, but also provides a useful method for the enantioselective synthesis of chiral triarylmethane derivatives.

Topics & Concepts

ChemistryEnantioselective synthesisCatalysisYield (engineering)Phosphoric acidSubstitution (logic)Organic chemistryCombinatorial chemistryMetallurgyProgramming languageMaterials scienceComputer scienceSynthesis of Indole Derivatives
Catalytic Asymmetric Substitution Reaction of 3-Substituted 2-Indolylmethanols with 2-Naphthols | Litcius