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Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. Part 1: Synthesis

Journal

TETRAHEDRON
Volume 63, Issue 18, Pages 3826-3839

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2007.02.038

Keywords

chlorin; hydroporphyrin; hydrodipyrrin; dipyrromethane

Funding

  1. NIGMS NIH HHS [R01 GM036238, R01 GM036238-20, R01 GM036238-18, R01 GM036238-19] Funding Source: Medline

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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)), and Pd(Il)] including the chlorin lacking any beta-pyrrole and meso substituents. (C) 2007 Elsevier Ltd. All rights reserved.

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