Literature DB >> 29261209

Synthesis of trifluoroalkyl or difluoroalkyl phenanthridine derivatives via cascade reaction using an intramolecular cyano group as a radical acceptor under photoredox catalysis.

Xu Liu1, Zhongjie Wu, Zeguo Zhang, Ping Liu, Peipei Sun.   

Abstract

In the presence of Ru(phen)3Cl2 or fac-Ir(ppy)3 under visible-light irradiation, the addition of fluorinated radicals to N-arylacrylamides followed by an intramolecular cyano group insertion cascade cyclization process produced trifluoroalkyl or difluoroalkyl phenanthridine derivatives in moderate to good yields. Three easily available fluoroalkylated reagents CF3SO2Cl, BrCF2CO2Et and BrCF2PO(OEt)2 were used as the sources of fluorinated radicals.

Entities:  

Year:  2018        PMID: 29261209     DOI: 10.1039/c7ob02804k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

Review 1.  Photocatalyzed syntheses of phenanthrenes and their aza-analogues. A review.

Authors:  Alessandra Del Tito; Havall Othman Abdulla; Davide Ravelli; Stefano Protti; Maurizio Fagnoni
Journal:  Beilstein J Org Chem       Date:  2020-06-25       Impact factor: 2.883

Review 2.  Progress in Difluoroalkylation of Organic Substrates by Visible Light Photoredox Catalysis.

Authors:  Agostinho Lemos; Christian Lemaire; André Luxen
Journal:  Adv Synth Catal       Date:  2019-01-17       Impact factor: 5.837

  2 in total

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