4.8 Article

Enantioselective Copper-Catalyzed Borylative Cyclization for the Synthesis of Quinazolinones

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 26, 页码 14355-14359

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202103259

关键词

asymmetric; boron; copper; cyclization; nitrogen-containing heterocycles

资金

  1. Leverhulme Trust (PDRA) [RPG-2016-360]
  2. European Union Horizon 2020 (Marie Sklodowska-Curie grant) [798846-CuCAN]
  3. Royal Government of Thailand (DPST scholarship)

向作者/读者索取更多资源

In this study, an enantioselective copper-catalyzed borylative cyclization was reported for the assembly of privileged pyrroloquinazolinone motifs. The reaction demonstrated high enantio- and diastereocontrol, yielding products with quaternary stereocenters. The utility of the products was further demonstrated through additional manipulations.
Quinazolinones are common substructures in molecules of medicinal importance. We report an enantioselective copper-catalyzed borylative cyclization for the assembly of privileged pyrroloquinazolinone motifs. The reaction proceeds with high enantio- and diastereocontrol, and can deliver products containing quaternary stereocenters. The utility of the products is demonstrated through further manipulations.

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