1382250-08-9

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 471239-60-8 di-tert-butyl (4-bromobenzene-1,2-diyl)biscarbamate 
• 1066-54-2 trimethylsilylacetylene 
• 1575-37-7 4-Bromo-benzene-1,2-diamine 

Downstream Products

• 1382250-10-3 di-tert-butyl(4-ethynyl-1,2-phenylene)dicarbamate 
• 1382250-12-5 (E)-3,4-bis(tert-butoxycarbonylamino)styrylboronic acid 
• 1382250-14-7 (E)-tert-butyl 4,4'-(ethene-1,2-diyl)bis(benzene-4,2,1-triyl)tetracarbamate 
• 1382250-16-9 tert-butyl 4,4'-(3-(4-(benzyloxy)phenyl)cyclopropane-1,2-diyl)bis(benzene-4,2,1-triyl)tetracarbamate 
• 1382250-18-1 4,4'-(3-(4-(benzyloxy)phenyl)cyclopropane-1,2-diyl)dibenzene-1,2-diamine 
• 1382650-12-5 (2S)-tert-butyl 2-(2-amino-4-(2-(4-amino-3-((S)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxamido)phenyl)-3-(4-(benzyloxy)phenyl)cyclopropyl)phenylcarbamoyl)pyrrolidine-1-carboxylate 
• 1382650-15-8 (2S,2'S)-tert-butyl 2,2'-(5,5'-(3-(4-(benzyloxy)phenyl)cyclopropane-1,2-diyl)bis(1H-benzo[d]imidazole-5,2-diyl))dipyrrolidine-1-carboxylate 
• 1382650-18-1 (S)-5,5'-(3-(4-(benzyloxy)phenyl)cyclopropane-1,2-diyl)bis(2-((S)-pyrrolidine-2-yl)-1H-benzo[d]imidazole) 
• 1382649-76-4 dimethyl (2S,2'S)-1,1'-((2S,2'S)-2,2'-(5,5'-(3-(4-(benzyloxy)phenyl)cyclopropane-1,2-diyl)bis(1H-benzo[d]imidazole-5,2-diyl))bis(pyrrolidine-2,1-diyl))bis(3-methyl-1-oxobutane-2,1-diyl)dicarbamate 
• 58297-31-7 4-ethynylbenzene-1,2-diamine 

Relevant academic research and scientific papers

Synthesis and Photophysical Properties of Triazolyl IrIIINucleosides

DNA-based nanomaterials are the subject of numerous researches. A series of modified nucleobases were synthesized either to construct a double helix where the natural H-bonded bases are replaced by metal-coordinated liganosides or to introduce a punctual modification inside a natural DNA structure. Thanks to their photophysical and photochemical properties, iridium(III) complexes are of increasing interest in the development of sensors and photoreactants for biochemical applications. In this view, we previously demonstrated that some IrIIIcomplexes are able to photoreact with DNA through photoinduced electron transfer. In this study, we report the synthesis and characterization of nucleosides bearing iridium complexes with unaltered properties compared to their parent complexes.

π-Extended Diaza[7]helicenes by Hybridization of Naphthalene Diimides and Hexa-peri-hexabenzocoronenes

The synthesis of an unprecedented, π-extended hexabenzocorene (HBC)-based diaza[7]helicene is presented. The target compound was synthesized by an ortho-fusion of two naphthalene diimide (NDI) units to a HBC-skeleton. A combination of Diels–Alder and Scho

ANTI-VIRAL COMPOUNDS

Compounds effective in inhibiting replication of Hepatitis C virus ("HCV") are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.