Results 181 to 190 of about 18,771 (284)

Double Click for Chirality: Chiral Dibenzo‐cycloocta‐bis‐triazoles via Strain‐Promoted Alkyne‐Azide Cycloaddition

open access: yesChemPhotoChem, EarlyView.
Strain‐promoted, double alkyne‐azide 1,3‐dipolar cycloadditions make dibenzo‐cycloocta‐bis‐triazoles which display a form of chirality that to date has been overlooked. The enantiomers can be resolved, with their remarkably high configurational stability being exemplified through a chiral fluorescent example.
Sebastian Pim   +7 more
wiley   +1 more source

The efficacy and safety of first-line monotherapies in primary therapy of invasive aspergillosis: a systematic review. [PDF]

open access: yesFront Pharmacol
Chen Y   +16 more
europepmc   +1 more source

4-[(E)-2-Furylmethyleneamino]-3-phenyl-1H-1,2,4-triazole-5(4H)-thione [PDF]

open access: gold, 2008
Hoong‐Kun Fun   +5 more
openalex   +1 more source

Chemistry of 1, 2, 4-Triazole: A Review Article

open access: yesInternational Journal of Science and Research (IJSR), 2016
openaire   +1 more source

Enhanced Performance of NiO‐Based Dye‐Sensitized Solar Cells Using a Covalent Porphyrin‐C60 Dyad

open access: yesChemPhotoChem, EarlyView.
The preparation and complete characterization of a covalent ZnPor‐C60 donor–acceptor dyad and its study in p‐type dye‐sensitized solar cells are described. This novel dyad contains an oligo(p‐phenylenevinylene) bridge, which elongates the distance between the electron donating and accepting units, leading in achieving significantly enhanced ...
Asterios Charisiadis   +6 more
wiley   +1 more source

4-[(E)-2,6-Dichlorobenzylideneamino]-3-{1-[4-(2-methylpropyl)phenyl]ethyl}-1H-1,2,4-triazole-5(4H)-thione [PDF]

open access: gold, 2008
Hoong‐Kun Fun   +6 more
openalex   +1 more source

Sustainable Synthesis of 1,2,3‐Triazoles using Cyrene as a Biodegradable Solvent in Click Chemistry

open access: yesChemSusChem, EarlyView.
Green triazoles: The first successful synthesis of 1,2,3‐triazoles using Cyrene as a biodegradable and non‐toxic solvent in click chemistry has been developed. This sustainable approach allows product isolation by simple precipitation in water, eliminating the need for organic solvent extractions and chromatographic purifications, thus minimizing waste
Andrea Citarella   +4 more
wiley   +1 more source

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