Issue 22, 2019

C31-Selective substitution of cationic N-heteroaromatic groups into a 3-vinylated chlorophyll-a derivative

Abstract

A variety of N-containing heteroarenes were site-selectively introduced at the C31-position of a chlorophyll-a derivative possessing a 3-vinyl group through a C–N+ bond via oxidative reactions using iodine in the presence of a silver(I) salt. Electron-rich N-heteroarenes were effectively substituted, while electron-withdrawing or bulky nitrogen-neighboring substituents suppressed the reactivities. The cationic products formed were characterized by 1D/2D NMR, and their optical properties were also investigated.

Graphical abstract: C31-Selective substitution of cationic N-heteroaromatic groups into a 3-vinylated chlorophyll-a derivative

Supplementary files

Article information

Article type
Communication
Submitted
17 Jan 2019
Accepted
05 Mar 2019
First published
06 Mar 2019

Org. Biomol. Chem., 2019,17, 5490-5495

C31-Selective substitution of cationic N-heteroaromatic groups into a 3-vinylated chlorophyll-a derivative

T. Takahashi, S. Ogasawara, S. Echizen, Y. Shinozaki and H. Tamiaki, Org. Biomol. Chem., 2019, 17, 5490 DOI: 10.1039/C9OB00130A

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