5 research outputs found
Novel podands containing N-arylthiosemicarbazide moiety
Six novel biological active podands based on N-arylthiosemicarbazide were synthesized from 1,5-bis(2-formylphenoxy)-3-oxapentane or 1,8-bis-(2-formylphenoxy)-3,6-dioxaoctane. All podands have tested cytotoxicity on human cancer cell lines RL, MCF7, RD, and HepG2 and antimicrobial activity. © ISUCT Publishing
Synthesis of tetrakisbenzo-31(34)-crown-7(8) ethers
Condensations of 1,5-bis(2-formylphenoxy)-3-oxapentane (1a) or 1,8-bis(2-formylphenoxy)-3,6-dioxanoctane (1b) podands and 1,8-bis(2-acetylphenoxy)-3,6-dioxanoctane (2) gave two novel crown ethers: tetrakis-(benzo)-31-crown-7 ether (5) and tetrakis(benzo)-34-crown-8 ether (6). Their molecular structures were established by IR, NMR and MS methods. © ISUCT Publishing
Novel podands containing N-arylthiosemicarbazide moiety
Six novel biological active podands based on N-arylthiosemicarbazide were synthesized from 1,5-bis(2-formylphenoxy)-3-oxapentane or 1,8-bis-(2-formylphenoxy)-3,6-dioxaoctane. All podands have tested cytotoxicity on human cancer cell lines RL, MCF7, RD, and HepG2 and antimicrobial activity. © ISUCT Publishing
Synthesis of tetrakisbenzo-31(34)-crown-7(8) ethers
Condensations of 1,5-bis(2-formylphenoxy)-3-oxapentane (1a) or 1,8-bis(2-formylphenoxy)-3,6-dioxanoctane (1b) podands and 1,8-bis(2-acetylphenoxy)-3,6-dioxanoctane (2) gave two novel crown ethers: tetrakis-(benzo)-31-crown-7 ether (5) and tetrakis(benzo)-34-crown-8 ether (6). Their molecular structures were established by IR, NMR and MS methods. © ISUCT Publishing