An aza-Diels-Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines.

Kim, Juhwan; Umerani, Mehran J; Kurakake, Reina; Qin, Huiting; Ziller, Joseph W; Gorodetsky, Alon A; Park, Young S

Kim, Juhwan; Umerani, Mehran J; Kurakake, Reina; Qin, Huiting; Ziller, Joseph W; Gorodetsky, Alon A; Park, Young S.

Afiliação

Kim J; Department of Chemical and Biomolecular Engineering, University of California, Irvine Irvine CA 92697 USA alon.gorodetsky@uci.edu.
Umerani MJ; Department of Materials Science and Engineering, University of California, Irvine Irvine CA 92697 USA.
Kurakake R; Department of Materials Science and Engineering, University of California, Irvine Irvine CA 92697 USA.
Qin H; Department of Chemical and Biomolecular Engineering, University of California, Irvine Irvine CA 92697 USA alon.gorodetsky@uci.edu.
Ziller JW; Department of Chemistry, University of California, Irvine Irvine CA 92697 USA.
Gorodetsky AA; Department of Chemical and Biomolecular Engineering, University of California, Irvine Irvine CA 92697 USA alon.gorodetsky@uci.edu.
Park YS; Department of Materials Science and Engineering, University of California, Irvine Irvine CA 92697 USA.

RSC Adv ; 11(23): 13722-13730, 2021 Apr 13.

Article em En | MEDLINE | ID: mdl-35423954

ABSTRACT

ABSTRACT

Quinolines and quinoline-containing macromolecules are renowned for their valuable biological activities and excellent materials properties. Herein, we validate a general strategy for the synthesis of chloro-containing quinoline, benzoquinoline and polybenzoquinoline variants via the aza-Diels-Alder reaction. The described findings could be ultimately implemented in other synthetic pathways and may open new opportunities for analogous quinoline-derived materials.

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2021 Tipo de documento: Article