Daisuke Taguchi, Takashi Nakamura, Hiroaki Horiuchi, Makoto Saikawa, Tatsuya Nabeshima
文献索引:10.1021/acs.joc.8b00782
全文:HTML全文
A series of selenophene-substituted boron-dipyrrin (BODIPY) monomers and selenophene-linked BODIPY oligomers was synthesized. The synthesized BODIPYs show good absorption/emission properties in the red to near-infrared region. Furthermore, some of the selenophenyl BODIPYs are not only useful fluorophores but also good photosensitizers to produce singlet oxygen.
Synthesis of 3,5-Disubstituted BODIPYs Bearing N-Containing ...
2018-04-17 [10.1021/acs.joc.8b00087] |
Steric Hindrance Underestimated: It is a Long, Long Way to T...
2018-04-17 [10.1021/acs.joc.8b00496] |
Stereoselective Sequential [4+2]/[2+2] Cycloadditions Involv...
2018-04-16 [10.1021/acs.joc.8b00346] |
Pd-Induced Double C–H Bond Activation in Annulative Synthese...
2018-04-16 [10.1021/acs.joc.8b00630] |
DiCE: Diastereomeric in Silico Chiral Elucidation, Expanded ...
2018-04-16 [10.1021/acs.joc.8b00338] |
首页 |
期刊大全 |
MSDS查询 |
化工产品分类 |
生物活性化合物 |
关于我们 |
免责声明:知识产权问题请联系 service1@chemsrc.com
Copyright © 2024 ChemSrc All Rights Reserved