A General and Practical Access to Chiral Quinoxalinones with Low Copper‐Catalyst Loading | Zendy

Tanimori Shinji | Zendy; Kashiwagi Hiroaki | Zendy; Nishimura Takeshi | Zendy; Kirihata Mitsunori | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

A General and Practical Access to Chiral Quinoxalinones with Low Copper‐Catalyst Loading

Author(s) -

Tanimori Shinji,

Kashiwagi Hiroaki,

Nishimura Takeshi,

Kirihata Mitsunori

Publication year - 2010

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.201000323

Subject(s) - copper , chemistry , catalysis , chloride , copper chloride , combinatorial chemistry , organic chemistry

A general, straightforward, and practical access to multi‐substituted chiral quinoxalin‐2‐ones has been achieved based on the copper(I) chloride‐dimethylethylenediamine (DMEDA) catalyst system. With the use of 1 mol% copper(I) chloride, structurally diverse quinoxalin‐2‐ones were generated with high optical purity from readily available starting materials, 2‐haloanilines and α‐amino acids, in a one‐pot manner.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research