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Published in 2025 at "Advanced Science"
DOI: 10.1002/advs.202570010
Abstract: Cyclic Ether‐Based Electrolytes The introduction of 1,8‐diazabicyclo[5.4.0]undec‐7‐ene (DBU) as an organic base additive completely inhibits the ring‐opening polymerization in DOL‐based electrolytes. The designed electrolyte exhibits a robust weak solvation structure, and rapid lithium‐ion transport dynamics,…
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Keywords:
temperature range;
lithium ion;
diazabicyclo undec;
undec ene ... See more keywords
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Published in 2023 at "International Journal of Energy Research"
DOI: 10.1155/2023/2171897
Abstract: Biodiesel is a promising alternative to petrodiesel, but its production from acid oils retains several technical challenges. Therefore, this study developed a new approach involving 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)-catalyzed one-pot reaction (simultaneous esterification-transesterification) to produce biodiesel with…
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Keywords:
reaction;
biodiesel;
one pot;
acid ... See more keywords
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Published in 2019 at "Journal of Chemical Research"
DOI: 10.1177/1747519819884146
Abstract: A facile and efficient method was developed for the preparation of a variety of aryl, heteroaryl, and alkyl N-sulfinyl imines using 1,8-diazabicyclo[5.4.0]undec-7-ene. In addition to tert-butanesulfinamide, the condensation is also effective with p-toluenesulfinamide. The reaction…
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Keywords:
diazabicyclo undec;
undec ene;
ene mediated;
sulfinyl imines ... See more keywords
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Published in 2022 at "Current organic synthesis"
DOI: 10.2174/1570179419666220831100708
Abstract: OBJECTIVE Misoprostol is a synthetic prostaglandin that is related structurally to naturally occurring prostaglandin (PG), and it has been acknowledged as an effective inhibitor of gastric acid secretion when administered intravenously. METHODS In the present…
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Keywords:
type misoprostol;
diazabicyclo undec;
misoprostol;
intramolecular isomerization ... See more keywords