nwch low

nwch low

27 followers
·
0 followers
nwch low
More ideas from nwch
https://doi.org/10.1016/j.tetlet.2017.10.005

https://doi.org/10.1016/j.tetlet.2017.10.005

https://doi.org/10.1016/j.dyepig.2017.10.017

https://doi.org/10.1016/j.dyepig.2017.10.017

https://doi.org/10.1016/j.tet.2017.10.064

https://doi.org/10.1016/j.tet.2017.10.064

https://doi.org/10.1016/j.dyepig.2017.10.017

https://doi.org/10.1016/j.dyepig.2017.10.017

Multinuclear NMR spectroscopy, photophysical, electrochemical and DNA-binding properties of fluorinated 1,8-naphthyridine-based boron heterocycles https://doi.org/10.1016/j.jfluchem.2017.11.006

Multinuclear NMR spectroscopy, photophysical, electrochemical and DNA-binding properties of fluorinated 1,8-naphthyridine-based boron heterocycles https://doi.org/10.1016/j.jfluchem.2017.11.006

A Copper-Catalyzed Tandem C–H ortho-Hydroxylation and N–N Bond-Formation Transformation: Expedited Synthesis of 1-(ortho-Hydroxyaryl)-1H-indazoles DOI: 10.1002/ejoc.201701149

A Copper-Catalyzed Tandem C–H ortho-Hydroxylation and N–N Bond-Formation Transformation: Expedited Synthesis of 1-(ortho-Hydroxyaryl)-1H-indazoles DOI: 10.1002/ejoc.201701149

https://doi.org/10.1016/j.tetlet.2017.11.032

https://doi.org/10.1016/j.tetlet.2017.11.032

New pyrrolo[3,2-b]pyrrole derivatives with multiple-acceptor substitution: Efficient fluorescent emission and near-infrared two-photon absorption https://doi.org/10.1016/j.tetlet.2017.11.028

New pyrrolo[3,2-b]pyrrole derivatives with multiple-acceptor substitution: Efficient fluorescent emission and near-infrared two-photon absorption https://doi.org/10.1016/j.tetlet.2017.11.028

Tetraphenylethylene- and fluorene-functionalized near-infrared aza-BODIPY dyes for living cell imaging DOI: 10.1039/C7RA10820F

Tetraphenylethylene- and fluorene-functionalized near-infrared aza-BODIPY dyes for living cell imaging DOI: 10.1039/C7RA10820F

Different Quenching Effect of Intramolecular Rotation on the Singlet and Triplet Excited States of Bodipy DOI: 10.1021/acs.jpcc.7b10466

Different Quenching Effect of Intramolecular Rotation on the Singlet and Triplet Excited States of Bodipy DOI: 10.1021/acs.jpcc.7b10466

DOI: 10.1002/chem.201704858

DOI: 10.1002/chem.201704858

One-pot heterocyclic ring closure of 1,1′-bi-2-naphthol to 7H-dibenzo[c,g]carbazole https://doi.org/10.1016/j.tetlet.2017.11.054

One-pot heterocyclic ring closure of 1,1′-bi-2-naphthol to 7H-dibenzo[c,g]carbazole https://doi.org/10.1016/j.tetlet.2017.11.054

NH Tautomerism of a Quadruply Fused Porphyrin: Rigid Fused Structure Delays the Proton Transfer DOI: 10.1021/acs.jpcb.7b10945

NH Tautomerism of a Quadruply Fused Porphyrin: Rigid Fused Structure Delays the Proton Transfer DOI: 10.1021/acs.jpcb.7b10945

Pyrrolo[2,3-d:5,4-d′]bisthiazoles: Alternate Synthetic Routes and a Comparative Study to Analogous Fused-Ring Bithiophenes DOI: 10.1021/acs.joc.7b02570

Pyrrolo[2,3-d:5,4-d′]bisthiazoles: Alternate Synthetic Routes and a Comparative Study to Analogous Fused-Ring Bithiophenes DOI: 10.1021/acs.joc.7b02570

Panchromatic Ternary Photovoltaic Cells Using a Nonfullerene Acceptor Synthesized Using C–H Functionalization  DOI: 10.1021/acs.chemmater.7b04499

Panchromatic Ternary Photovoltaic Cells Using a Nonfullerene Acceptor Synthesized Using C–H Functionalization DOI: 10.1021/acs.chemmater.7b04499

Structural Tuning of Boron Difluoride Formazanate Electrochemiluminescence Mediated by Tri-n-propylamine DOI: 10.1021/acs.jpcc.7b10246

Structural Tuning of Boron Difluoride Formazanate Electrochemiluminescence Mediated by Tri-n-propylamine DOI: 10.1021/acs.jpcc.7b10246