| Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. I. Synthesis. | |
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MedLine Citation:
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PMID: 17479168 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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Five routes to stable chlorins bearing 0 or 1 meso substituents have been investigated, among which reaction of a 9-bromo-1-formyldipyrromethane and 2,3,4,5-tetrahydro-1,3,3-trimethyldipyrrin proved most effective. Application of this route afforded metallochlorins [Cu(II), Zn(II), Pd(II)] including the chlorin lacking any beta-pyrrole and meso substituents. |
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Authors:
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Marcin Ptaszek; Brian E McDowell; Masahiko Taniguchi; Han-Je Kim; Jonathan S Lindsey |
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Publication Detail:
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Type: JOURNAL ARTICLE |
Journal Detail:
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Title: Tetrahedron Volume: 63 ISSN: 0040-4020 ISO Abbreviation: Tetrahedron Publication Date: 2007 Apr |
Date Detail:
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Created Date: 2009-3-5 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 2984170R Medline TA: Tetrahedron Country: - |
Other Details:
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Languages: ENG Pagination: 3826-3839 Citation Subset: - |
Affiliation:
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Department of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA. |
Export Citation:
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Descriptor/Qualifier:
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| Grant Support | |
ID/Acronym/Agency:
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R01 GM036238-18//NIGMS NIH HHS; R01 GM036238-19//NIGMS NIH HHS; R01 GM036238-20//NIGMS NIH HHS |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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