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[ASAP] Mechanochemical Synthesis of Primary Amides
[ASAP] Recovery of Critical Metals from Aqueous Sources

[ASAP] Machine Learning: New Ideas and Tools in Environmental Science and Engineering

[ASAP] General Mechanochemical Synthetic Protocol to Late Transition Metal–NHC (N-Heterocyclic Carbene) Complexes

[ASAP] Importance of Thermal Stability Data to Avoid Dangerous Reagents: Temozolomide Case Study

[ASAP] Allenone-Mediated Racemization/Epimerization-Free Peptide Bond Formation and Its Application in Peptide Synthesis

Heterogeneous Palladium Catalysts for Decarbonylation of Biomass-Derived Molecules under Mild Conditions
METROHMF, algae
Workin′ 6 to 5: A highly active heterogeneous catalyst, Pd/SBA-15(DP), promotes the selective decarbonylation of biomass-derived HMF to furfural alcohol with a high yield, up to 96 %, in mild conditions. The route offers a simple and effective method of linking C6 and C5 molecules in the biomass conversion value chain. In addition to HMF the catalyst is effective towards the decarbonylation of other biomass-derived aldehydes, also.
Preparation of Imines by Oxidative Coupling of Benzyl Alcohols with Amines Catalysed by Dicopper Complexes
Abstract
Complexation of 2,7-bis(2-pyridyl)-1,8-naphthyridine (bpnp) with Cu2O in formic acid under aerobic conditions provided a dicopper complex [Cu2(bpnp)(μ-OH)(HCOO)3] (1). This complex has been characterized by X-ray crystallographic and spectroscopic analysis. With O2 as the oxidant, complex 1 is an efficient catalyst for the oxidative coupling of alcohols with amines or diamines, leading to the corresponding imines or diimines in good to excellent yields.
A dicopper complex has been found to be an efficient catalyst for the oxidative coupling of benzyl alcohols with amines or diamines, leading to the corresponding imines or diimines in good to excellent yields without using any organic solvent.