| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270002 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Three new phenothiazine-corrole dyads were prepared by the reaction of phenothiazine-10-carbonyl chloride and mono-hydroxyl triaryl corrole in the presence of DBU. As compared to corrole monomer, these phenothiazine-corrole dyads exhibit significant enhanced DNA photocleavage activity as compared to corrole monomer precursors.
Graphical abstractThree new phenothiazine-corrole dyads were prepared by the reaction of phenothiazine-10-carbonyl chloride and mono-hydroxyl triaryl corrole in the presence of DBU. These phenothiazine-corrole dyads exhibit significant enhanced DNA photocleavage activity as compared to corrole monomer precursors.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lei Shi, Hai-Yang Liu, Kai-Mei Peng, Xiang-Li Wang, Li-Li You, Jun Lu, Lei Zhang, Hui Wang, Liang-Nian Ji, Huan-Feng Jiang,