前田大光 先生(立命館大)と久木一朗 先生(大阪大)の共著論文が掲載されました。
Doubly N-Methylated Porphyrinoids
Wakana Naito, Nobuhiro Yasuda, Tatsuki Morimoto, Yasuteru Shigeta, Hikaru Takaya, Ichiro Hisaki, and Hiromitsu Maeda*
Org. Lett. 2016, 18, 3006–3009.
DOI: 10.1021/acs.orglett.6b01377
Abstract
Chirality-induced aromatic π-electronic macrocycles, porphyrin and corroles, were synthesized through doubly inner N-methylation through multistep and one-pot reactions, respectively. The exact structures of doubly N-methylated porphyrin and corroles were revealed by single-crystal synchrotron X-ray analysis, exhibiting two N-methyl groups located on neighboring pyrrole rings in up/down conformations. These doubly inner N-substitutions of the π-electronic macrocycles induced distorted geometries, resulting in chiroptical properties after optical resolutions.
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