Abstract
The readily available tetrakis(4-hydroxyphenyl)porphyrin core 1 was silylated to the trisprotected 2a and the tetraprotected 3a. These two molecules were used, respectively as monomers and core reagents in a synthesis of pentaporphyrin dendrimers 7a-c with benzyl ether branches or hexadecyl groups as the peripheral groups.
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Smeets, S., Roex, H., & Dehaen, W. (2003). Asymmetrically protected porphyrin meso-tetraphenols and their applicationin the synthesis of pentaporphyrin dendrimers. Arkivoc, 2003(4), 83–92. https://doi.org/10.3998/ark.5550190.0004.407
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