Synthesis of 5,10,15,20-tetra(N-methyl-6-quinolyl)-21,23-dithiaporphyrin chloride as cationic core-modified porphyrin

Research output: Contribution to journalArticle

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Abstract

First cationic 6-quinolyl substituted dithiaporphyrin was synthesized using Skraup quinoline methodology from thiaporphyrin bearing 4-acetamidophenyl prepared by condensation reaction of aromatic aldehyde with pyrrole.

Original languageEnglish (US)
Pages (from-to)1261-1264
Number of pages4
JournalChinese Chemical Letters
Volume15
Issue number11
StatePublished - Nov 2004

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Bearings (structural)
Pyrroles
Condensation reactions
Porphyrins
Aldehydes
Chlorides
quinoline
21,23-dithiaporphyrin

Keywords

  • Dilithiophen
  • Porphyrin
  • Telomerase inhibitor
  • Thiaporphyrin

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Synthesis of 5,10,15,20-tetra(N-methyl-6-quinolyl)-21,23-dithiaporphyrin chloride as cationic core-modified porphyrin. / Lu, Tao; Hurley, Laurence.

In: Chinese Chemical Letters, Vol. 15, No. 11, 11.2004, p. 1261-1264.

Research output: Contribution to journalArticle

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abstract = "First cationic 6-quinolyl substituted dithiaporphyrin was synthesized using Skraup quinoline methodology from thiaporphyrin bearing 4-acetamidophenyl prepared by condensation reaction of aromatic aldehyde with pyrrole.",
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AU - Hurley, Laurence

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KW - Telomerase inhibitor

KW - Thiaporphyrin

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