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Quoted phrase not found in phrase index: "b-resorcylaldehyde"
Page 1
Complete Reconstitution and Deorphanization of the 3 MDa Nocardiosis-Associated Polyketide Synthase.
Yuet KP, Liu CW, Lynch SR, Kuo J, Michaels W, Lee RB, McShane AE, Zhong BL, Fischer CR, Khosla C. Yuet KP, et al. J Am Chem Soc. 2020 Apr 1;142(13):5952-5957. doi: 10.1021/jacs.0c00904. Epub 2020 Mar 20. J Am Chem Soc. 2020. PMID: 32182063 Free PMC article.
The NOCAP aglycone has an unprecedented structure comprised of a substituted resorcylaldehyde headgroup linked to a 15-carbon tail that harbors two conjugated all-trans trienes separated by a stereogenic hydroxyl group. ...
The NOCAP aglycone has an unprecedented structure comprised of a substituted resorcylaldehyde headgroup linked to a 15-carbon tail th …
Total Synthesis of (-)-Peniphenone A.
Pantin M, Brimble MA, Furkert DP. Pantin M, et al. J Org Chem. 2018 Jul 6;83(13):7049-7059. doi: 10.1021/acs.joc.7b03231. Epub 2018 Mar 5. J Org Chem. 2018. PMID: 29480005
The synthesis was achieved in 14 steps (longest linear sequence) from commercially available 2,4-dihydroxybenzaldehyde in 6% overall yield. Investigations into a parallel approach required extension of Krische's enantioselective hydrogen-mediated C-C coupling …
The synthesis was achieved in 14 steps (longest linear sequence) from commercially available 2,4-dihydroxybenzaldehyde
Silver(I) complexes of 2,4-dihydroxybenzaldehyde-amino acid Schiff bases-Novel noncompetitive alpha-glucosidase inhibitors.
Zheng J, Ma L. Zheng J, et al. Bioorg Med Chem Lett. 2015;25(10):2156-61. doi: 10.1016/j.bmcl.2015.03.078. Epub 2015 Mar 31. Bioorg Med Chem Lett. 2015. PMID: 25881823
A series of silver(I) complexes of 2,4-dihydroxybenzaldehyde-amino acid Schiff bases were designed and tested for alpha-glucosidase inhibition. ...
A series of silver(I) complexes of 2,4-dihydroxybenzaldehyde-amino acid Schiff bases were designed and tested for alpha …
2,4-Dinitrophenylhydrazones of 2,4-dihydroxybenzaldehyde, 2,4-dihydroxyacetophenone and 2,4-dihydroxybenzophenone.
Baughman RG, Martin KL, Singh RK, Stoffer JO. Baughman RG, et al. Acta Crystallogr C. 2004 Feb;60(Pt 2):o103-6. doi: 10.1107/S0108270103027197. Epub 2004 Jan 10. Acta Crystallogr C. 2004. PMID: 14767127
In 2,4-dihydroxybenzaldehyde 2,4-dinitrophenylhydrazone N,N-dimethylformamide solvate [or 4-[(2,4-dinitrophenyl)hydrazonomethyl]benzene-1,3-diol N,N-dimethylformamide solvate], C(13)H(10)N(4)O(6).C(3)H(7)NO, (X), 2,4-dihydroxyacetophenone 2,4-dinitrophenylhyd …
In 2,4-dihydroxybenzaldehyde 2,4-dinitrophenylhydrazone N,N-dimethylformamide solvate [or 4-[(2,4-dinitrophenyl)hydrazo …
Modification of silica nanoparticles by 2,4-dihydroxybenzaldehyde and 5-bromosalicylaldehyde as new nanocomposites for efficient removal and preconcentration of Cu(ii) and Cd(ii) ions from water, blood, and fish muscles.
Gad HM, El Rayes SM, Abdelrahman EA. Gad HM, et al. RSC Adv. 2022 Jul 1;12(30):19209-19224. doi: 10.1039/d2ra03177a. eCollection 2022 Jun 29. RSC Adv. 2022. PMID: 35865597 Free PMC article.
Herein, silica nanoparticles were modified by 2,4-dihydroxybenzaldehyde and 5-bromosalicylaldehyde to produce new nanocomposites which were abbreviated as N(1) and N(2), respectively. ...
Herein, silica nanoparticles were modified by 2,4-dihydroxybenzaldehyde and 5-bromosalicylaldehyde to produce new nanoc …
Rapid, selective, direct and derivative spectrophotometric determination of titanium with 2,4-dihydroxybenzaldehyde isonicotinoyl hydrazone.
Babaiah O, Kesava Rao C, Sreenivasulu Reddy T, Krishna Reddy V. Babaiah O, et al. Talanta. 1996 Apr;43(4):551-8. doi: 10.1016/0039-9140(95)01766-6. Talanta. 1996. PMID: 18966518
The metal ion forms a reddish brown coloured complex with 2,4-dihydroxybenzaldehyde isonicotinoyl hydrazone (2,4-DHBINH) in the pH range 1-7. ...
The metal ion forms a reddish brown coloured complex with 2,4-dihydroxybenzaldehyde isonicotinoyl hydrazone (2,4-DHBINH …
Theoretical investigation of the Zn2+ detection mechanism based on the quinoline derivative of the Schiff-base receptor.
Wen J, Xia Y, Ding S, Liu Y. Wen J, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2023 Feb 15;287(Pt 1):122123. doi: 10.1016/j.saa.2022.122123. Epub 2022 Nov 17. Spectrochim Acta A Mol Biomol Spectrosc. 2023. PMID: 36423505
The sensing mechanism of the quinoline-derived Schiff base HL (concentrated from 8-hydroxyquinoline with 2,4-dihydroxybenzaldehyde) as a highly selective fluorescent probe for Zn(2+) was investigated by theoretical calculations with DFT and TDDFT. ...
The sensing mechanism of the quinoline-derived Schiff base HL (concentrated from 8-hydroxyquinoline with 2,4-dihydroxybenza
Synthesis, characterization of ruthenium(II), nickel(II), palladium(II), and platinum(II) triphenylphosphine-based complexes bearing an ONS-donor chelating agent: Interaction with biomolecules, antioxidant, in vitro cytotoxic, apoptotic activity and cell cycle analysis.
Elsayed SA, Badr HE, di Biase A, El-Hendawy AM. Elsayed SA, et al. J Inorg Biochem. 2021 Oct;223:111549. doi: 10.1016/j.jinorgbio.2021.111549. Epub 2021 Jul 21. J Inorg Biochem. 2021. PMID: 34315119
Four new transition metal complexes, [M(PPh(3))(L)](.)CH(3)OH (M = Ni(II) (1), Pd(II) (2)) [Pt (PPh(3))(2)(HL)]Cl (3) and [Ru(CO)(PPh(3))(2)(L)] (4) (H(2)L = 2,4-dihydroxybenzaldehyde-S-methyldithiocarbazate, PPh(3) = triphenylphosphine) have been synthesized …
Four new transition metal complexes, [M(PPh(3))(L)](.)CH(3)OH (M = Ni(II) (1), Pd(II) (2)) [Pt (PPh(3))(2)(HL)]Cl (3) and [Ru(CO)(PPh(3))(2) …
One-pot green synthesis of 1,3,5-triarylpentane-1,5-dione and triarylmethane derivatives as a new class of tyrosinase inhibitors.
Zheng ZP, Zhang YN, Zhang S, Chen J. Zheng ZP, et al. Bioorg Med Chem Lett. 2016 Feb 1;26(3):795-798. doi: 10.1016/j.bmcl.2015.12.092. Epub 2015 Dec 28. Bioorg Med Chem Lett. 2016. PMID: 26754613
A new method was developed for one-pot green synthesis 1,3,5-triarylpentane-1,5-dione, triarylmethane, and flavonoid derivatives from the reaction between 2,4-dihydroxybenzaldehyde and hydroxyacetophenones via Aldol, Michael, and Friedel-Crafts additions usin …
A new method was developed for one-pot green synthesis 1,3,5-triarylpentane-1,5-dione, triarylmethane, and flavonoid derivatives from the re …
56 results