40248-63-3Relevant articles and documents
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McCasland et al.
, p. 2399,2401 Anm. 18 (1959)
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New copper(II) 2-(alkylamino)troponates
Barret, Marie C.,Bhatia, Purvi H.,Kociok-Koehn, Gabriele,Molloy, Kieran C.
, p. 543 - 551 (2014/08/05)
The copper aminotropones Cu[ON(R′)C7H4R-4] 2 [R = H, R′ = Me (13), Et (14), n-Pr (15), n-Bu (16), Bz (17), MenOCH2CH2 (20); R = i-Pr, R′ = Me (18), n-Pr (19), MenOCH2CH2 (21)] have been prepared from the corresponding aminotropones HN(R′)OC7H4R-4 (1-7) by reacting with copper(II) acetate in aqueous ethanol. 20, 21 contain the flavourant, menthol, as part of the ligand. The structures of 5 (R = H, R′ = Bz), a hydrogen-bonded dimer, 14 and 20, both incorporating square-planar, four-coordinate copper centres, have been determined by X-ray crystallography. The antibacterial activities of complexes 13, 17, 20 and 21 have been assayed against Staphylococcus waneri, an in vitro model of plaque inhibition effects, and found to be more active than a commercial toothpaste formulation, but less active than the O,O-chelated copper(II) complex of ethylmaltol.
Chemical resolution of (±)-calanolide A, (±)-cordatolide A and their 11-demethyl analogues
Ma, Tao,Gao, Qi,Chen, Zhiwei,Wang, Lin,Liu, Gang
, p. 1079 - 1083 (2008/12/20)
The chemical resolution of (±)-calanolide A and (±)-cordatolide A into their corresponding optically active enantiomers is described. Their inhibitory activities against HIV-1 are tested in vitro.