Issue 48, 2020

Synthesis of N-methylated unsymmetric porphyrinoids with restricted N-centered chirality from chlorophyll-a

Abstract

Regioselectively N-methylated chlorophyll-a derivatives were prepared as their cationic and hydrophilic species. Both their epimerically pure samples at the chiral methylated nitrogen atom were obtained, and the stereochemistry was proposed by circular dichroism spectral analysis. This is the first example for restricted N-centered chirality in an unsymmetric chlorin core.

Graphical abstract: Synthesis of N-methylated unsymmetric porphyrinoids with restricted N-centered chirality from chlorophyll-a

Supplementary files

Article information

Article type
Communication
Submitted
26 Oct 2020
Accepted
26 Nov 2020
First published
26 Nov 2020

Org. Biomol. Chem., 2020,18, 9800-9804

Synthesis of N-methylated unsymmetric porphyrinoids with restricted N-centered chirality from chlorophyll-a

Y. Kawamoto, Y. Nagano, Y. Kitagawa and H. Tamiaki, Org. Biomol. Chem., 2020, 18, 9800 DOI: 10.1039/D0OB02146F

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