An Overview on the Synthesis of Lamellarins and Related Compounds with Biological Interest
Lamellarins are natural products with a [3,4]-fused pyrrolocoumarin skeleton possessing interesting biological properties. More than 70 members have been isolated from diverse marine organisms, such as sponges, ascidians, mollusks, and tunicates.
Vasiliki-Panagiota M. Mitsiou +3 more
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Due to boron’s metalloid properties, aromatic boron reagents are prevalent synthetic intermediates. The direct borylation of aryl C-H bonds for producing aromatic boron compounds offers an appealing, one-step solution.
Manhong Li +6 more
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Crystal structures of zinc(II) coordination complexes with isoquinoline N-oxide
The reaction of one equivalent of zinc(II) halide salts with two equivalents of isoquinoline N-oxide (iQNO; C9H7NO) in methanol yields compounds of the general formula [ZnX2(iQNO)2], with X = Cl− (I), Br− (II) and I− (III). However, starting with zinc(II)
Erin N. Groneck +3 more
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INTERACTION OF COAL TAR QUINOLINE BASES WITH ION EXCHANGERS IN THE FORM OF COPPER CATIONS
Sorption of quinoline, isoquinoline, and quinaldine by copper forms of polymeric zirconium phosphate and strong acid polystyrene-divinylbenzene cation-exchanger from aqueous solutions was investigated.
O. S. Zabarina, E. V. Ostapova
doaj
Divergent synthesis of indenoisoquinolines and indenoisochromenes by rhodium-catalysed cyclocondensation of <i>N</i>-substituted benzamides with 2-diazoindenediones. [PDF]
Kim DY, Kimura Y, Miura R, Kondo T.
europepmc +1 more source
Directing group-assisted C-H functionalization of 2-arylbenzo[<i>f</i>]isoquinoline: a robust route to decumbenine B analogues with photophysical applications. [PDF]
Mondal S +9 more
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Iterative enrichment cultivation and multiomic analysis reveal potential endophytic bacteria affecting the sinomenine synthesis in Sinomenium acutum. [PDF]
Yin S +6 more
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Genome-wide transcriptional and metabolic responses of Eschscholzia californica to salt stress. [PDF]
Huang Z +8 more
europepmc +1 more source
Multitargeted Aza-Arylcarboxamides for Neurodegenerative Diseases: Potent Histamine H<sub>3</sub> Receptor Ligands with Anticholinesterase and Metal-Chelating Activities. [PDF]
Lopes FB +4 more
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