Cinnamic acid derivatives in tuberculosis, malaria and cardiovascular diseases-a review

P De, F Bedos-Belval… - Current Organic …, 2012 - ingentaconnect.com
Cinnamic acid and its phenolic analogues are natural substances. Chemically, cinnamic
acids or the 3-phenyl acrylic acids, offer three main reactive sites: substitution on the phenyl …

Novel 1, 4-naphthoquinone-based sulfonamides: Synthesis, QSAR, anticancer and antimalarial studies

R Pingaew, V Prachayasittikul… - European Journal of …, 2015 - Elsevier
Abstract A novel series of 1, 4-naphthoquinones (33–44) tethered by open and closed chain
sulfonamide moieties were designed, synthesized and evaluated for their cytotoxic and …

p‐Nitrobenzyloxycarbonyl (pNZ) as a Temporary Nα‐Protecting Group in Orthogonal Solid‐Phase Peptide Synthesis – Avoiding Diketopiperazine and Aspartimide …

A Isidro‐Llobet, J Guasch‐Camell, M Álvarez… - 2005 - Wiley Online Library
Abstract p‐Nitrobenzyloxycarbonyl (pNZ) was used as a temporary protecting group for α‐
amino functionalities in solid‐phase peptide synthesis. The corresponding derivatives are …

Structure–activity relationships of novel anti-malarial agents. Part 2: Cinnamic acid derivatives

J Wiesner, A Mitsch, P Wißner, H Jomaa… - Bioorganic & medicinal …, 2001 - Elsevier
We have described compound 1 as a lead structure for a novel class of anti-malarial agents.
Replacement of the 3-phenylpropionyl moiety of the lead structure 1 by a 4-propoxycinnamic …

Selective N-Alkylation of Aminobenzenesulfonamides with Alcohols for the Synthesis of Amino-(N-alkyl)benzenesulfonamides Catalyzed by a Metal–Ligand …

L Shen, X Wu, L Shi, X Xu, J Zhang… - The Journal of Organic …, 2024 - ACS Publications
[(p-Cymene) Ru (2, 2′-bpyO)(H2O)] was proven to be an efficient catalyst for the synthesis
of amino-(N-alkyl) benzenesulfonamides via selective N-alkylation of …

Progresses in the pursuit of aldose reductase inhibitors: the structure-based lead optimization step

A Ramunno, S Cosconati, S Sartini, V Maglio… - European journal of …, 2012 - Elsevier
Aldose reductase (ALR2) is a crucial enzyme in the development of the major complications
of diabetes mellitus. Very recently it has been demonstrated that the ARL2 inhibitor …

Photochemical modulation of Ras‐mediated signal transduction using caged farnesyltransferase inhibitors: Activation by one‐and two‐photon excitation

D Abate‐Pella, NA Zeliadt, JD Ochocki… - …, 2012 - Wiley Online Library
The creation of caged molecules involves the attachment of protecting groups to biologically
active compounds such as ligands, substrates and drugs that can be removed under specific …

Organic compounds

F Shi, H Renes, E Van Ommeren, SM Vorster… - US Patent …, 2020 - Google Patents
R, is an alkyl residue containing 6 to 20 carbon atoms, or an alkene residue containing from
9 to 25 carbon atoms with 1 to 6 double bonds, R, together with the carbonyl group to which …

Green synthesis of spirooxindole-pyrrolidine/piperidine fused nitrochromane: One pot three component stereo and regioselective cycloaddition

S Nayak, SK Mishra, S Bhakta, P Panda… - Letters in Organic …, 2016 - ingentaconnect.com
Background: Now a day's green synthesis for multicomponent reactions is a powerful tool for
construction of five membered/six membered heterocyclic ring systems. The synthesis of …

N-acyl-amino acid derivatives for improvement of the flavor profile of edible compositions

F Shi, H Renes, E Van Ommeren, SM Vorster… - US Patent …, 2020 - Google Patents
US10856563B2 - N-acyl-amino acid derivatives for improvement of the flavor profile of edible
compositions - Google Patents US10856563B2 - N-acyl-amino acid derivatives for improvement …