Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin

P. A. Liddell; X. Zarate; Ana Moore; Thomas Moore; D. Gust

doi:10.1016/S0040-4039(00)01740-8

Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin

P. A. Liddell
, X. Zarate
, Ana Moore
, Thomas Moore
, D. Gust

Molecular Sciences, School of (SMS)

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

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 language	English (US)
Pages (from-to)	9661-9665
Number of pages	5
Journal	Tetrahedron Letters
Volume	41
Issue number	49
DOIs	https://doi.org/10.1016/S0040-4039(00)01740-8
State	Published - Dec 2 2000

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin",

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.",

author = "Liddell, \{P. A.\} and X. Zarate and Ana Moore and Thomas Moore and D. Gust",

note = "Funding Information: This work was supported by the US Department of Energy (DE-FG03-93ER14404). It is publication 438 from the ASU Center for the Study of Early Events in Photosynthesis. The mass spectra data was obtained at the Nebraska Center for Mass Spectrometry.",

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AU - Liddell, P. A.

AU - Zarate, X.

AU - Moore, Ana

AU - Moore, Thomas

AU - Gust, D.

N1 - Funding Information: This work was supported by the US Department of Energy (DE-FG03-93ER14404). It is publication 438 from the ASU Center for the Study of Early Events in Photosynthesis. The mass spectra data was obtained at the Nebraska Center for Mass Spectrometry.

PY - 2000/12/2

Y1 - 2000/12/2

N2 - 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.

AB - 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.

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 49

ER -

Synthesis of a carotenobenzoporphyrin from a meso-diphenylporphyrin

Abstract

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