| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1315681 | Journal of Fluorine Chemistry | 2006 | 6 Pages | 
Abstract
												A strong DNA cleavage property switched by photo irradiation was found for 9-anthracenecarboxylic acid substituted gem-difluorocyclopropane derivatives; in particular, a clear contrast in the activity was observed between the enantiomers of (S,S)- and (R,R)-3-aminomethyl-2,2-difluorocyclopropylmethyl 9-anthracenecarboxylate.
Graphical abstractA unique DNA cleavage property switched by photo irradiation was found for anthracene–cyclopropane hybrids compounds. Figure optionsDownload full-size imageDownload as PowerPoint slide
Keywords
												
											Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Inorganic Chemistry
												
											Authors
												Keiko Ninomiya, Kunihiko Tanimoto, Nanae Ishida, Daisuke Horii, Masahiko Sisido, Toshiyuki Itoh, 
											