Rational design of supramolecular chirality in porphyrin assemblies: the halogen bond case‡
Literature Information
Sankar Muniappan, Sophia Lipstman, Israel Goldberg
Asymmetric functionalization of the tetraarylporphyrin scaffold, combined with directional supramolecular halogen bonding, yields chiral architectures.
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![(4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure (4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure](https://static.chemtradehub.com/structs/184/18411-75-1-d4cd.webp)



