Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin

P. A. Liddell, X. Zarate, Ana L Moore, Thomas A Moore, John Devens Gust

Research output: Contribution to journalArticle

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Abstract

A carotenobenzoporphyrin has been prepared by covalently joining a benzoporphyrin derivative and an anilinocarotenoid by an amide linkage. A synthetic meso-diphenylporphyrin is the precursor of the benzoporphyrin moiety. The carotenobenzoporphyrin is highly fluorescent and does not sensitize measurable amounts of singlet oxygen. (C) 2000 Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)9661-9665
Number of pages5
JournalTetrahedron Letters
Volume41
Issue number49
Publication statusPublished - Dec 2 2000

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Singlet Oxygen
Amides
Joining
Derivatives

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin. / Liddell, P. A.; Zarate, X.; Moore, Ana L; Moore, Thomas A; Gust, John Devens.

In: Tetrahedron Letters, Vol. 41, No. 49, 02.12.2000, p. 9661-9665.

Research output: Contribution to journalArticle

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